Origins of DLBCL genes
Tier 1, high-confidence DLBCL genes
125 total
Tier 2, low-confidence DLBCL genes
210 total
Tier 3, retired DLBCL genes
387 total
References
1.
Lohr
JG, Stojanov P, Lawrence MS, Auclair D, Chapuy B, Sougnez C,
Cruz-Gordillo P, Knoechel B, Asmann YW, Slager SL, Novak AJ, Dogan A,
Ansell SM, Link BK, Zou L, Gould J, Saksena G, Stransky N,
Rangel-Escareño C, Fernandez-Lopez JC, Hidalgo-Miranda A,
Melendez-Zajgla J, Hernández-Lemus E, Schwarz-Cruz y Celis A,
Imaz-Rosshandler I, Ojesina AI, Jung J, Pedamallu CS, Lander ES,
Habermann TM, Cerhan JR, Shipp MA, Getz G, Golub TR. Discovery and
prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by
whole-exome sequencing. Proc Natl Acad Sci U S A. 2012 Mar
6;109(10):3879–3884. PMCID: PMC3309757
2.
Dreval K, Hilton LK, Cruz M, Shaalan H,
Ben-Neriah S, Boyle M, Collinge B, Coyle KM, Duns G, Farinha P, Grande
BM, Meissner B, Pararajalingam P, Rushton CK, Slack GW, Wong J, Mungall
AJ, Marra MA, Connors JM, Steidl C, Scott DW, Morin RD. Genetic
subdivisions of follicular lymphoma defined by distinct coding and
noncoding mutation patterns. Blood. 2023 Aug 10;142(6):561–573. PMCID:
PMC10644066
3.
Wienand K, Chapuy B, Stewart C, Dunford AJ, Wu
D, Kim J, Kamburov A, Wood TR, Cader FZ, Ducar MD, Thorner AR, Nag A,
Heubeck AT, Buonopane MJ, Redd RA, Bojarczuk K, Lawton LN, Armand P,
Rodig SJ, Fromm JR, Getz G, Shipp MA. Genomic analyses of flow-sorted
Hodgkin Reed-Sternberg cells reveal complementary
mechanisms of immune evasion. Blood Adv. 2019 Dec 10;3(23):4065–4080.
PMCID: PMC6963251
4.
Fan
Z, Pei R, Sha K, Chen L, Wang T, Lu Y. Comprehensive characterization of
driver genes in diffuse large B cell lymphoma. Oncol Lett.
2020 Jul;20(1):382–390. PMCID: PMC7285964
5.
Desch AK, Hartung K, Botzen A, Brobeil A,
Rummel M, Kurch L, Georgi T, Jox T, Bielack S, Burdach S, Classen CF,
Claviez A, Debatin KM, Ebinger M, Eggert A, Faber J, Flotho C, Frühwald
M, Graf N, Jorch N, Kontny U, Kramm C, Kulozik A, Kühr J, Sykora KW,
Metzler M, Müller HL, Nathrath M, Nüßlein T, Paulussen M, Pekrun A,
Reinhardt D, Reinhard H, Rössig C, Sauerbrey A, Schlegel PG, Schneider
DT, Scheurlen W, Schweigerer L, Simon T, Suttorp M, Vorwerk P, Schmitz
R, Kluge R, Mauz-Körholz C, Körholz D, Gattenlöhner S, Bräuninger A. Genotyping circulating
tumor DNA of pediatric Hodgkin lymphoma.
Leukemia. 2020 Jan;34(1):151–166.
6.
Hübschmann D, Kleinheinz K, Wagener R, Bernhart
SH, López C, Toprak UH, Sungalee S, Ishaque N, Kretzmer H, Kreuz M,
Waszak SM, Paramasivam N, Ammerpohl O, Aukema SM, Beekman R, Bergmann
AK, Bieg M, Binder H, Borkhardt A, Borst C, Brors B, Bruns P, Carrillo
de Santa Pau E, Claviez A, Doose G, Haake A, Karsch D, Haas S, Hansmann
ML, Hoell JI, Hovestadt V, Huang B, Hummel M, Jäger-Schmidt C,
Kerssemakers JNA, Korbel JO, Kube D, Lawerenz C, Lenze D, Martens JHA,
Ott G, Radlwimmer B, Reisinger E, Richter J, Rico D, Rosenstiel P,
Rosenwald A, Schillhabel M, Stilgenbauer S, Stadler PF, Martín-Subero
JI, Szczepanowski M, Warsow G, Weniger MA, Zapatka M, Valencia A,
Stunnenberg HG, Lichter P, Möller P, Loeffler M, Eils R, Klapper W,
Hoffmann S, Trümper L, ICGC MMML-Seq consortium, ICGC DE-Mining
consortium, BLUEPRINT consortium, Küppers R, Schlesner M, Siebert R.
Mutational mechanisms shaping the coding and noncoding genome of
germinal center derived B-cell lymphomas.
Leukemia. 2021 Jul;35(7):2002–2016. PMCID: PMC8257491
7.
Spina V, Khiabanian H, Messina M, Monti S,
Cascione L, Bruscaggin A, Spaccarotella E, Holmes AB, Arcaini L, Lucioni
M, Tabbò F, Zairis S, Diop F, Cerri M, Chiaretti S, Marasca R, Ponzoni
M, Deaglio S, Ramponi A, Tiacci E, Pasqualucci L, Paulli M, Falini B,
Inghirami G, Bertoni F, Foà R, Rabadan R, Gaidano G, Rossi D. The
genetics of nodal marginal zone lymphoma. Blood. 2016 Sep
8;128(10):1362–1373. PMCID: PMC5016706
8.
Zhang J, Grubor V, Love CL, Banerjee A,
Richards KL, Mieczkowski PA, Dunphy C, Choi W, Au WY, Srivastava G,
Lugar PL, Rizzieri DA, Lagoo AS, Bernal-Mizrachi L, Mann KP, Flowers C,
Naresh K, Evens A, Gordon LI, Czader M, Gill JI, Hsi ED, Liu Q, Fan A,
Walsh K, Jima D, Smith LL, Johnson AJ, Byrd JC, Luftig MA, Ni T, Zhu J,
Chadburn A, Levy S, Dunson D, Dave SS. Genetic heterogeneity of diffuse
large B-cell lymphoma. Proceedings of the
National Academy of Sciences of the United States of America.
2013;110:1398–1403. PMCID: PMC3557051
9.
Barisic D, Chin CR, Meydan C, Teater M, Tsialta
I, Mlynarczyk C, Chadburn A, Wang X, Sarkozy M, Xia M, Carson SE,
Raggiri S, Debek S, Pelzer B, Durmaz C, Deng Q, Lakra P, Rivas M, Steidl
C, Scott DW, Weng AP, Mason CE, Green MR, Melnick A. ARID1A
orchestrates SWI/SNF-mediated
sequential binding of transcription factors with ARID1A
loss driving pre-memory B cell fate and
lymphomagenesis. Cancer Cell. 2024 Apr 8;42(4):583–604.e11.
10.
Krysiak K, Gomez F, White BS, Matlock M, Miller
CA, Trani L, Fronick CC, Fulton RS, Kreisel F, Cashen AF, Carson KR,
Berrien-Elliott MM, Bartlett NL, Griffith M, Griffith OL, Fehniger TA.
Recurrent somatic mutations affecting B-cell
receptor signaling pathway genes in follicular lymphoma. Blood. 2017 Jan
26;129(4):473–483. PMCID: PMC5270390
11.
Love C, Sun Z, Jima D, Li G, Zhang J, Miles R,
Richards KL, Dunphy CH, Choi WWL, Srivastava G, Lugar PL, Rizzieri DA,
Lagoo AS, Bernal-Mizrachi L, Mann KP, Flowers CR, Naresh KN, Evens AM,
Chadburn A, Gordon LI, Czader MB, Gill JI, Hsi ED, Greenough A, Moffitt
AB, McKinney M, Banerjee A, Grubor V, Levy S, Dunson DB, Dave SS. The
genetic landscape of mutations in Burkitt lymphoma. Nat
Genet. 2012 Dec;44(12):1321–1325. PMCID: PMC3674561
12.
Rossi D, Trifonov V, Fangazio M, Bruscaggin A,
Rasi S, Spina V, Monti S, Vaisitti T, Arruga F, Famà R, Ciardullo C,
Greco M, Cresta S, Piranda D, Holmes A, Fabbri G, Messina M, Rinaldi A,
Wang J, Agostinelli C, Piccaluga PP, Lucioni M, Tabbò F, Serra R,
Franceschetti S, Deambrogi C, Daniele G, Gattei V, Marasca R, Facchetti
F, Arcaini L, Inghirami G, Bertoni F, Pileri SA, Deaglio S, Foà R,
Dalla-Favera R, Pasqualucci L, Rabadan R, Gaidano G. The coding genome
of splenic marginal zone lymphoma: Activation of NOTCH2 and
other pathways regulating marginal zone development. J Exp Med. 2012 Aug
27;209(9):1537–1551. PMCID: PMC3428941
13.
Reddy A, Zhang J, Davis NS, Moffitt AB, Love
CL, Waldrop A, Leppa S, Pasanen A, Meriranta L, Karjalainen-Lindsberg
ML, Nørgaard P, Pedersen M, Gang AO, Høgdall E, Heavican TB, Lone W,
Iqbal J, Qin Q, Li G, Kim SY, Healy J, Richards KL, Fedoriw Y,
Bernal-Mizrachi L, Koff JL, Staton AD, Flowers CR, Paltiel O,
Goldschmidt N, Calaminici M, Clear A, Gribben J, Nguyen E, Czader MB,
Ondrejka SL, Collie A, Hsi ED, Tse E, Au-Yeung RKH, Kwong YL, Srivastava
G, Choi WWL, Evens AM, Pilichowska M, Sengar M, Reddy N, Li S, Chadburn
A, Gordon LI, Jaffe ES, Levy S, Rempel R, Tzeng T, Happ LE, Dave T,
Rajagopalan D, Datta J, Dunson DB, Dave SS. Genetic and Functional
Drivers of Diffuse Large B Cell Lymphoma. Cell. 2017
Oct;171(2):481–494.e15. PMCID: PMC5659841
14.
Camacho E, Hernández L, Hernández S, Tort F,
Bellosillo B, Beà S, Bosch F, Montserrat E, Cardesa A, Fernández PL,
Campo E. ATM gene
inactivation in mantle cell lymphoma mainly occurs by truncating
mutations and missense mutations involving the phosphatidylinositol-3
kinase domain and is associated with increasing numbers of chromosomal
imbalances. Blood. 2002 Jan 1;99(1):238–244.
15.
Beà
S, Valdés-Mas R, Navarro A, Salaverria I, Martín-Garcia D, Jares P, Giné
E, Pinyol M, Royo C, Nadeu F, Conde L, Juan M, Clot G, Vizán P, Croce
LD, Puente DA, López-Guerra M, Moros A, Roue G, Aymerich M, Villamor N,
Colomo L, Martínez A, Valera A, Martín-Subero JI, Amador V, Hernández L,
Rozman M, Enjuanes A, Forcada P, Muntañola A, Hartmann EM, Calasanz MJ,
Rosenwald A, Ott G, Hernández-Rivas JM, Klapper W, Siebert R, Wiestner
A, Wilson WH, Colomer D, López-Guillermo A, López-Otín C, Puente XS,
Campo E. Landscape of
somatic mutations and clonal evolution in mantle cell lymphoma.
PNAS. 2013;110(45):18250–18255.
16.
Braggio E, Dogan A, Keats JJ, Chng WJ, Huang G,
Matthews JM, Maurer MJ, Law ME, Bosler DS, Barrett M, Lossos IS, Witzig
TE, Fonseca R. Genomic analysis of marginal zone and lymphoplasmacytic
lymphomas identified common and disease-specific abnormalities. Mod
Pathol. 2012 May;25(5):651–660. PMCID: PMC3341516
17.
Morin RD, Mendez-Lago M, Mungall AJ, Goya R,
Mungall KL, Corbett RD, Johnson NA, Severson TM, Chiu R, Field M,
Jackman S, Krzywinski M, Scott DW, Trinh DL, Tamura-Wells J, Li S, Firme
MR, Rogic S, Griffith M, Chan S, Yakovenko O, Meyer IM, Zhao EY, Smailus
D, Moksa M, Chittaranjan S, Rimsza L, Brooks-Wilson A, Spinelli JJ,
Ben-Neriah S, Meissner B, Woolcock B, Boyle M, McDonald H, Tam A, Zhao
Y, Delaney A, Zeng T, Tse K, Butterfield Y, Birol I, Holt R, Schein J,
Horsman DE, Moore R, Jones SJM, Connors JM, Hirst M, Gascoyne RD, Marra
MA. Frequent mutation of histone-modifying genes in
non-Hodgkin lymphoma. Nature. 2011 Jul
27;476(7360):298–303. PMCID: PMC3210554
18.
Challa-Malladi M, Lieu YK, Califano O, Holmes
AB, Bhagat G, Murty VV, Dominguez-Sola D, Pasqualucci L, Dalla-Favera R.
Combined genetic inactivation of Β2-Microglobulin and
CD58 reveals frequent escape from immune recognition in
diffuse large B cell lymphoma. Cancer Cell. 2011 Dec
13;20(6):728–740. PMCID: PMC3660995
19.
Pararajalingam P, Coyle KM, Arthur SE, Thomas
N, Alcaide M, Meissner B, Boyle M, Qureshi Q, Grande BM, Rushton C,
Slack GW, Mungall AJ, Tam CS, Agarwal R, Dawson SJ, Lenz G,
Balasubramanian S, Gascoyne RD, Steidl C, Connors J, Villa D, Audas TE,
Marra MA, Johnson NA, Scott DW, Morin RD. Coding and noncoding drivers
of mantle cell lymphoma identified through exome and genome sequencing.
Blood. 2020 Jul 30;136(5):572–584. PMCID: PMC7440974
20.
Reichel J, Chadburn A, Rubinstein PG,
Giulino-Roth L, Tam W, Liu Y, Gaiolla R, Eng K, Brody J, Inghirami G,
Carlo-Stella C, Santoro A, Rahal D, Totonchy J, Elemento O, Cesarman E,
Roshal M. Flow
sorting and exome sequencing reveal the oncogenome of primary
Hodgkin and Reed-Sternberg cells. Blood.
2015 Feb 12;125(7):1061–1072.
21.
Xia
M, David L, Teater M, Gutierrez J, Wang X, Meydan C, Lytle A, Slack GW,
Scott DW, Morin RD, Onder O, Elenitoba-Johnson KSJ, Zamponi N,
Cerchietti L, Lu T, Philippar U, Fontan L, Wu H, Melnick AM. BCL10
Mutations Define Distinct Dependencies Guiding Precision Therapy
for DLBCL. Cancer Discov. 2022 Aug 5;12(8):1922–1941.
PMCID: PMC9357155
22.
Russler-Germain DA, Krysiak K, Ramirez CA,
Mosior M, Watkins MP, Gomez F, Skidmore ZL, Trani L, Gao F, Geyer S,
Cashen A, Mehta-Shah N, Kahl B, Bartlett N, Alderuccio J, Lossos I,
Ondrejka S, Hsi E, Martin P, Leonard J, Griffith M, Griffith O, Fehniger
T. Mutations
associated with progression in follicular lymphoma predict inferior
outcomes at diagnosis: Alliance A151303. Blood
Advances. 2023;7:5524–5539.
23.
Tanaka S, Louie DC, Kant JA, Reed JC. Frequent incidence of
somatic mutations in translocated BCL2 oncogenes of
non-Hodgkin’s lymphomas. Blood. 1992 Jan
1;79(1):229–237.
24.
Burkhardt B, Michgehl U, Rohde J, Erdmann T,
Berning P, Reutter K, Rohde M, Borkhardt A, Burmeister T, Dave S,
Tzankov A, Dugas M, Sandmann S, Fend F, Finger J, Mueller S, Gökbuget N,
Haferlach T, Kern W, Hartmann W, Klapper W, Oschlies I, Richter J,
Kontny U, Lutz M, Maecker-Kolhoff B, Ott G, Rosenwald A, Siebert R, von
Stackelberg A, Strahm B, Woessmann W, Zimmermann M, Zapukhlyak M, Grau
M, Lenz G. Clinical relevance of molecular characteristics in
Burkitt lymphoma differs according to age. Nat Commun. 2022
Jul 6;13(1):3881. PMCID: PMC9259584
25.
Sarkozy C, Hung SS, Chavez EA, Duns G, Takata
K, Chong LC, Aoki T, Jiang A, Miyata-Takata T, Telenius A, Slack GW,
Molina TJ, Ben-Neriah S, Farinha P, Dartigues P, Damotte D, Mottok A,
Salles GA, Casasnovas RO, Savage KJ, Laurent C, Scott DW,
Traverse-Glehen A, Steidl C. Mutational landscape of
gray zone lymphoma. Blood. 2021 Apr 1;137(13):1765–1776.
26.
Mascle X, Albagli O, Lemercier C. Point mutations in
BCL6 DNA-binding domain reveal distinct
roles for the six zinc fingers. Biochem Biophys Res Commun. 2003 Jan
10;300(2):391–396.
27.
Baliñas-Gavira C, Rodríguez MI, Andrades Á,
Cuadros M, Álvarez-Pérez J, Álvarez-Prado ÁF, Yébenes VG de,
Sanchez-Hernandez S, Fernández-Vigo E, Muñoz J, Martín F, Ramiro A,
Martinez-Climent J, Medina P. Frequent mutations in
the amino-terminal domain of BCL7A impair its tumor
suppressor role in DLBCL. Leukemia. 2020;1–14.
28.
Grande BM, Gerhard DS, Jiang A, Griner NB,
Abramson JS, Alexander TB, Allen H, Ayers LW, Bethony JM, Bhatia K,
Bowen J, Casper C, Choi JK, Culibrk L, Davidsen TM, Dyer MA,
Gastier-Foster JM, Gesuwan P, Greiner TC, Gross TG, Hanf B, Harris NL,
He Y, Irvin JD, Jaffe ES, Jones SJM, Kerchan P, Knoetze N, Leal FE,
Lichtenberg TM, Ma Y, Martin JP, Martin MR, Mbulaiteye SM, Mullighan CG,
Mungall AJ, Namirembe C, Novik K, Noy A, Ogwang MD, Omoding A, Orem J,
Reynolds SJ, Rushton CK, Sandlund JT, Schmitz R, Taylor C, Wilson WH,
Wright GW, Zhao EY, Marra MA, Morin RD, Staudt LM. Genome-wide discovery
of somatic coding and noncoding mutations in pediatric endemic and
sporadic Burkitt lymphoma. Blood. 2019;133(12):1313–1324.
PMCID: PMC6428665
29.
Tiacci E, Trifonov V, Schiavoni G, Holmes A,
Kern W, Martelli MP, Pucciarini A, Bigerna B, Pacini R, Wells VA,
Sportoletti P, Pettirossi V, Mannucci R, Elliott O, Liso A, Ambrosetti
A, Pulsoni A, Forconi F, Trentin L, Semenzato G, Inghirami G, Capponi M,
Di Raimondo F, Patti C, Arcaini L, Musto P, Pileri S, Haferlach C,
Schnittger S, Pizzolo G, Foà R, Farinelli L, Haferlach T, Pasqualucci L,
Rabadan R, Falini B. BRAF mutations in hairy-cell leukemia.
N Engl J Med. 2011 Jun 16;364(24):2305–2315. PMCID: PMC3689585
30.
Wan
PTC, Garnett MJ, Roe SM, Lee S, Niculescu-Duvaz D, Good VM, Jones CM,
Marshall CJ, Springer CJ, Barford D, Marais R, Cancer Genome Project. Mechanism of
activation of the RAF-ERK signaling pathway by oncogenic
mutations of B-RAF. Cell. 2004 Mar 19;116(6):855–867.
31.
Almasmoum HA, Airhihen B, Seedhouse C, Winkler
GS. Frequent
loss of BTG1 activity and impaired interactions with the
Caf1 subunit of the Ccr4-Not deadenylase in
non-Hodgkin lymphoma. Leuk Lymphoma. 2021
Feb;62(2):281–290.
32.
Albuquerque MA, Grande BM, Ritch EJ,
Pararajalingam P, Jessa S, Krzywinski M, Grewal JK, Shah SP, Boutros PC,
Morin RD. Enhancing knowledge discovery from cancer genomics data with
Galaxy. Gigascience. 2017 May 1;6(5):1–13. PMCID: PMC5437943
33.
Hu
N, Wang F, Sun T, Xu Z, Zhang J, Bernard D, Xu S, Wang S, Kaminski M,
Devata S, Phillips T, Malek SN. Follicular Lymphoma-associated BTK Mutations are
Inactivating Resulting in Augmented AKT
Activation. Clin Cancer Res. 2021 Apr 15;27(8):2301–2313. PMCID:
PMC8046715
34.
Lenz G, Davis RE, Ngo VN, Lam L, George TC,
Wright GW, Dave SS, Zhao H, Xu W, Rosenwald A, Ott G, Müller-Hermelink
HK, Gascoyne RD, Connors JM, Rimsza LM, Campo E, Jaffe ES, Delabie J,
Smeland EB, Fisher RI, Chan WC, Staudt LM. Oncogenic
CARD11 mutations in human diffuse large B cell
lymphoma. Science. 2008 Mar;319(5870):1676–1679.
35.
Wu
C, de Miranda NF, Chen L, Wasik AM, Mansouri L, Jurczak W, Galazka K,
Dlugosz-Danecka M, Machaczka M, Zhang H, Peng R, Morin RD, Rosenquist R,
Sander B, Pan-Hammarström Q. Genetic heterogeneity in primary and
relapsed mantle cell lymphomas: Impact of recurrent
CARD11 mutations. Oncotarget. 2016 Jun
21;7(25):38180–38190. PMCID: PMC5122381
36.
Yan
Q, Huang Y, Watkins AJ, Kocialkowski S, Zeng N, Hamoudi RA, Isaacson PG,
de Leval L, Wotherspoon A, Du MQ. BCR and TLR
signaling pathways are recurrently targeted by genetic changes in
splenic marginal zone lymphomas. Haematologica. 2012 Apr;97(4):595–598.
PMCID: PMC3347666
37.
Schmitz R, Young RM, Ceribelli M, Jhavar S,
Xiao W, Zhang M, Wright G, Shaffer AL, Hodson DJ, Buras E, Liu X, Powell
J, Yang Y, Xu W, Zhao H, Kohlhammer H, Rosenwald A, Kluin P,
Müller-Hermelink HK, Ott G, Gascoyne RD, Connors JM, Rimsza LM, Campo E,
Jaffe ES, Delabie J, Smeland EB, Ogwang MD, Reynolds SJ, Fisher RI,
Braziel RM, Tubbs RR, Cook JR, Weisenburger DD, Chan WC, Pittaluga S,
Wilson W, Waldmann TA, Rowe M, Mbulaiteye SM, Rickinson AB, Staudt LM.
Burkitt lymphoma pathogenesis and therapeutic targets from structural
and functional genomics. Nature. 2012 Oct 4;490(7418):116–120. PMCID: PMC3609867
38.
Jallades L, Baseggio L, Sujobert P, Huet S,
Chabane K, Callet-Bauchu E, Verney A, Hayette S, Desvignes JP, Salgado
D, Levy N, Béroud C, Felman P, Berger F, Magaud JP, Genestier L, Salles
G, Traverse-Glehen A. Exome sequencing identifies recurrent
BCOR alterations and the absence of KLF2,
TNFAIP3 and MYD88 mutations in splenic diffuse
red pulp small B-cell lymphoma.
Haematologica. 2017 Oct;102(10):1758–1766. PMCID: PMC5622860
39.
Richter J, Schlesner M, Hoffmann S, Kreuz M,
Leich E, Burkhardt B, Rosolowski M, Ammerpohl O, Wagener R, Bernhart SH,
Lenze D, Szczepanowski M, Paulsen M, Lipinski S, Russell RB, Adam-Klages
S, Apic G, Claviez A, Hasenclever D, Hovestadt V, Hornig N, Korbel JO,
Kube D, Langenberger D, Lawerenz C, Lisfeld J, Meyer K, Picelli S,
Pischimarov J, Radlwimmer B, Rausch T, Rohde M, Schilhabel M, Scholtysik
R, Spang R, Trautmann H, Zenz T, Borkhardt A, Drexler HG, Möller P,
MacLeod RAF, Pott C, Schreiber S, Trümper L, Loeffler M, Stadler PF,
Lichter P, Eils R, Küppers R, Hummel M, Klapper W, Rosenstiel P,
Rosenwald A, Brors B, Siebert R, ICGC MMML-Seq Project. Recurrent mutation of the
ID3 gene in Burkitt lymphoma identified by
integrated genome, exome and transcriptome sequencing. Nat Genet.
2012 Dec;44(12):1316–1320.
40.
Schneider M, Schneider S, Zühlke-Jenisch R,
Klapper W, Sundström C, Hartmann S, Hansmann ML, Siebert R, Küppers R,
Giefing M. Alterations of
the CD58 gene in classical Hodgkin
lymphoma. Genes Chromosomes Cancer. 2015 Oct;54(10):638–645.
41.
Nie
M, Ren W, Ye X, Berglund M, Wang X, Fjordén K, Du L, Giannoula Y, Lei D,
Su W, Li W, Liu D, Linderoth J, Jiang C, Bao H, Jiang W, Huang H, Hou Y,
Zhu S, Enblad G, Jerkeman M, Wu K, Zhang H, Amini RM, Li ZM,
Pan-Hammarström Q. The dual role of CD70 in B-cell lymphomagenesis. Clin Transl Med. 2022
Dec;12(12):e1118. PMCID: PMC9722974
42.
Davis RE, Ngo VN, Lenz G, Tolar P, Young RM,
Romesser PB, Kohlhammer H, Lamy L, Zhao H, Yang Y, Xu W, Shaffer AL,
Wright G, Xiao W, Powell J, Jiang JK, Thomas CJ, Rosenwald A, Ott G,
Müller-Hermelink HK, Gascoyne RD, Connors JM, Johnson NA, Rimsza LM,
Campo E, Jaffe ES, Wilson WH, Delabie J, Smeland EB, Fisher RI, Braziel
RM, Tubbs RR, Cook JR, Weisenburger DD, Chan WC, Pierce SK, Staudt LM.
Chronic active B-cell-receptor signalling in
diffuse large B-cell lymphoma. Nature. 2010
Jan;463(7277):88–92. PMCID: PMC2845535
43.
Panea R, Love C, Shingleton JR, Reddy A, Bailey
J, Moormann A, Otieno J, Ong’echa J, Oduor C, Schroêder K, Masalu N,
Chao N, Agajanian M, Major M, Fedoriw Y, Richards K, Rymkiewicz G, Miles
R, Alobeid B, Bhagat G, Flowers C, Ondrejka S, Hsi E, Choi W, Au-Yeung
R, Hartmann W, Lenz G, Meyerson H, Lin YY, Zhuang Y, Luftig M, Waldrop
A, Dave T, Thakkar D, Sahay H, Li G, Palus B, Seshadri V, Kim S,
Gascoyne R, Levy S, Mukhopadhyay M, Dunson D, Dave S. The whole genome
landscape of Burkitt lymphoma subtypes. Blood. 2019;
44.
Morin RD, Mungall K, Pleasance E, Mungall AJ,
Goya R, Huff RD, Scott DW, Ding J, Roth A, Chiu R, Corbett RD, Chan FC,
Mendez-Lago M, Trinh DL, Bolger-Munro M, Taylor G, Hadj Khodabakhshi A,
Ben-Neriah S, Pon J, Meissner B, Woolcock B, Farnoud N, Rogic S, Lim EL,
Johnson NA, Shah S, Jones S, Steidl C, Holt R, Birol I, Moore R, Connors
JM, Gascoyne RD, Marra MA. Mutational and structural analysis of diffuse
large B-cell lymphoma using whole-genome
sequencing. Blood. 2013 Aug 15;122(7):1256–1265. PMCID: PMC3744992
45.
Duns G, Viganò E, Ennishi D, Sarkozy C, Hung
SS, Chavez E, Takata K, Rushton C, Jiang A, Ben-Neriah S, Woolcock BW,
Slack GW, Hsi ED, Craig JW, Hilton LK, Shah SP, Farinha P, Mottok A,
Gascoyne RD, Morin RD, Savage KJ, Scott DW, Steidl C. Characterization of
DLBCL with a PMBL gene expression
signature. Blood. 2021 Jul 15;138(2):136–148.
46.
Kannengiesser C, Brookes S, del Arroyo AG, Pham
D, Bombled J, Barrois M, Mauffret O, Avril MFM, Chompret A, Lenoir GM,
Sarasin A, French Hereditary Melanoma Study Group, Peters G, Bressac-de
Paillerets B. Functional,
structural, and genetic evaluation of 20 CDKN2A germ line
mutations identified in melanoma-prone families or patients. Hum
Mutat. 2009 Apr;30(4):564–574.
47.
Mottok A, Woolcock B, Chan FC, Tong KM, Chong
L, Farinha P, Telenius A, Chavez E, Ramchandani S, Drake M, Boyle M,
Ben-Neriah S, Scott DW, Rimsza LM, Siebert R, Gascoyne RD, Steidl C. Genomic
Alterations in CIITA Are Frequent in
Primary Mediastinal Large B Cell Lymphoma and Are
Associated with Diminished MHC Class II
Expression. Cell Rep. 2015 Nov 17;13(7):1418–1431.
48.
Pasqualucci L, Dominguez-Sola D, Chiarenza A,
Fabbri G, Grunn A, Trifonov V, Kasper LH, Lerach S, Tang H, Ma J, Rossi
D, Chadburn A, Murty VV, Mullighan CG, Gaidano G, Rabadan R, Brindle PK,
Dalla-Favera R. Inactivating mutations of acetyltransferase genes in
B-cell lymphoma. Nature. 2011 Mar
10;471(7337):189–195. PMCID: PMC3271441
49.
Parry M, Rose-Zerilli MJJ, Gibson J, Ennis S,
Walewska R, Forster J, Parker H, Davis Z, Gardiner A, Collins A, Oscier
DG, Strefford JC. Whole exome sequencing identifies novel recurrently
mutated genes in patients with splenic marginal zone lymphoma. PLoS One.
2013;8(12):e83244. PMCID: PMC3862727
50.
Khodabakhshi AH, Morin RD, Fejes AP, Mungall
AJ, Mungall KL, Bolger-Munro M, Johnson NA, Connors JM, Gascoyne RD,
Marra MA, Birol I, Jones SJM. Recurrent targets of aberrant somatic
hypermutation in lymphoma. Oncotarget. 2012;3(11):1308–1319. PMCID: PMC3717795
51.
Zmajkovicova K, Pawar S, Maier-Munsa S,
Maierhofer B, Wiest I, Skerlj R, Taveras AG, Badarau A.
Genotype-phenotype correlations in WHIM syndrome: A
systematic characterization of CXCR4WHIM variants. Genes
Immun. 2022 Sep;23(6):196–204. PMCID: PMC9519442
52.
Gong C, Krupka JA, Gao J, Grigoropoulos NF,
Giotopoulos G, Asby R, Screen M, Usheva Z, Cucco F, Barrans S, Painter
D, Zaini NBM, Haupl B, Bornelöv S, Ruiz De Los Mozos I, Meng W, Zhou P,
Blain AE, Forde S, Matthews J, Khim Tan MG, Burke GAA, Sze SK, Beer P,
Burton C, Campbell P, Rand V, Turner SD, Ule J, Roman E, Tooze R,
Oellerich T, Huntly BJ, Turner M, Du MQ, Samarajiwa SA, Hodson DJ. Sequential inverse
dysregulation of the RNA helicases DDX3X and
DDX3Y facilitates MYC-driven
lymphomagenesis. Molecular Cell. 2021;
53.
Mottok A, Hung SS, Chavez EA, Woolcock B,
Telenius A, Chong LC, Meissner B, Nakamura H, Rushton C, Viganò E,
Sarkozy C, Gascoyne RD, Connors JM, Ben-Neriah S, Mungall A, Marra MA,
Siebert R, Scott DW, Savage KJ, Steidl C. Integrative genomic
analysis identifies key pathogenic mechanisms in primary mediastinal
large B-cell lymphoma. Blood. 2019 Sep
5;134(10):802–813.
54.
Gomez F, Fisk B, McMichael JF, Mosior M, Foltz
JA, Skidmore ZL, Duncavage EJ, Miller CA, Abel H, Li YS, Russler-Germain
DA, Krysiak K, Watkins MP, Ramirez CA, Schmidt A, Martins Rodrigues F,
Trani L, Khanna A, Wagner JA, Fulton RS, Fronick CC, O’Laughlin MD,
Schappe T, Cashen AF, Mehta-Shah N, Kahl BS, Walker J, Bartlett NL,
Griffith M, Fehniger TA, Griffith OL. Ultra-Deep Sequencing
Reveals the Mutational Landscape of Classical
Hodgkin Lymphoma. Cancer Res Commun. 2023 Nov 15;3(11):2312–2330.
PMCID: PMC10648575
55.
Bohle V, Döring C, Hansmann M-L, Küppers R. Role of early B-cell factor 1 (EBF1) in
Hodgkin lymphoma. Leukemia. 2013 Mar;27(3):671–679.
56.
Ramírez-Komo JA, Delaney MA, Straign D, Lukin
K, Tsang M, Iritani BM, Hagman J. Spontaneous loss of B
lineage transcription factors leads to pre-B leukemia in
Ebf1+/-Bcl-xLTg mice.
Oncogenesis. 2017 Jul 10;6(7):e355. PMCID: PMC5541707
57.
Thomas N, Dreval K, Gerhard DS, Hilton LK,
Abramson JS, Ambinder RF, Barta S, Bartlett NL, Bethony J, Bhatia K,
Bowen J, Bryan AC, Cesarman E, Casper C, Chadburn A, Cruz M, Dittmer DP,
Dyer MA, Farinha P, Gastier-Foster JM, Gerrie AS, Grande BM, Greiner T,
Griner NB, Gross TG, Harris NL, Irvin JD, Jaffe ES, Henry D, Huppi R,
Leal FE, Lee MS, Martin JP, Martin MR, Mbulaiteye SM, Mitsuyasu R,
Morris V, Mullighan CG, Mungall AJ, Mungall K, Mutyaba I, Nokta M,
Namirembe C, Noy A, Ogwang MD, Omoding A, Orem J, Ott G, Petrello H,
Pittaluga S, Phelan JD, Ramos JC, Ratner L, Reynolds SJ, Rubinstein PG,
Sissolak G, Slack G, Soudi S, Swerdlow SH, Traverse-Glehen A, Wilson WH,
Wong J, Yarchoan R, ZenKlusen JC, Marra MA, Staudt LM, Scott DW, Morin
RD. Genetic subgroups inform on pathobiology in adult and pediatric
Burkitt lymphoma. Blood. 2023 Feb 23;141(8):904–916. PMCID:
PMC10023728
58.
Chapuy B, Stewart C, Dunford AJ, Kim J,
Kamburov A, Redd RA, Lawrence MS, Roemer MGM, Li AJ, Ziepert M, Staiger
AM, Wala JA, Ducar MD, Leshchiner I, Rheinbay E, Taylor-Weiner A,
Coughlin CA, Hess JM, Pedamallu CS, Livitz D, Rosebrock D, Rosenberg M,
Tracy AA, Horn H, van Hummelen P, Feldman AL, Link BK, Novak AJ, Cerhan
JR, Habermann TM, Siebert R, Rosenwald A, Thorner AR, Meyerson ML, Golub
TR, Beroukhim R, Wulf GG, Ott G, Rodig SJ, Monti S, Neuberg DS, Loeffler
M, Pfreundschuh M, Trümper L, Getz G, Shipp MA. Molecular subtypes of
diffuse large B cell lymphoma are associated with distinct
pathogenic mechanisms and outcomes. Nat Med. 2018 May;24(5):679–690.
PMCID: PMC6613387
59.
Wang Q, Dong S, Yao H, Wen L, Qiu H, Qin L, Ma
L, Chen S. ETV6 mutation in a cohort of 970 patients with
hematologic malignancies. Haematologica. 2014 Oct;99(10):e176–178.
PMCID: PMC4181263
60.
Morin RD, Johnson NA, Severson TM, Mungall AJ,
An J, Goya R, Paul JE, Boyle M, Woolcock BW, Kuchenbauer F, Yap D,
Humphries RK, Griffith OL, Shah S, Zhu H, Kimbara M, Shashkin P, Charlot
JF, Tcherpakov M, Corbett R, Tam A, Varhol R, Smailus D, Moksa M, Zhao
Y, Delaney A, Qian H, Birol I, Schein J, Moore R, Holt R, Horsman DE,
Connors JM, Jones S, Aparicio S, Hirst M, Gascoyne RD, Marra MA. Somatic
mutations altering EZH2 (Tyr641) in follicular
and diffuse large B-cell lymphomas of
germinal-center origin. Nat Genet. 2010 Feb;42(2):181–185. PMCID: PMC2850970
61.
Sneeringer CJ, Scott MP, Kuntz KW, Knutson SK,
Pollock RM, Richon VM, Copeland RA. Coordinated activities of wild-type
plus mutant EZH2 drive tumor-associated hypertrimethylation
of lysine 27 on histone H3 (H3K27) in human
B-cell lymphomas. Proc Natl Acad Sci U S A.
2010 Dec 7;107(49):20980–20985. PMCID: PMC3000297
62.
Scholl V, Stefanoff CG, Hassan R, Spector N,
Renault IZ. Mutations within the 5’
region of FAS/CD95 gene in nodal diffuse large
B-cell lymphoma. Leuk Lymphoma. 2007
May;48(5):957–963.
63.
Wang L, Yang JK, Kabaleeswaran V, Rice AJ, Cruz
AC, Park AY, Yin Q, Damko E, Jang SB, Raunser S, Robinson CV, Siegel RM,
Walz T, Wu H. The Fas-FADD death domain complex structure
reveals the basis of DISC assembly and disease mutations.
Nat Struct Mol Biol. 2010 Nov;17(11):1324–1329. PMCID: PMC2988912
64.
Arthur SE, Jiang A, Grande BM, Alcaide M,
Cojocaru R, Rushton CK, Mottok A, Hilton LK, Lat PK, Zhao EY, Culibrk L,
Ennishi D, Jessa S, Chong L, Thomas N, Pararajalingam P, Meissner B,
Boyle M, Davidson J, Bushell KR, Lai D, Farinha P, Slack GW, Morin GB,
Shah S, Sen D, Jones SJM, Mungall AJ, Gascoyne RD, Audas TE, Unrau P,
Marra MA, Connors JM, Steidl C, Scott DW, Morin RD. Genome-wide
discovery of somatic regulatory variants in diffuse large B-cell lymphoma. Nat Commun. 2018 Oct 1;9(1):4001.
PMCID: PMC6167379
65.
Duan S, Cermak L, Pagan JK, Rossi M, Martinengo
C, di Celle PF, Chapuy B, Shipp M, Chiarle R, Pagano M.
FBXO11 targets BCL6 for degradation and is
inactivated in diffuse large B-cell
lymphomas. Nature. 2011 Nov;
66.
Saffie R, Zhou N, Rolland D, Önder Ö, Basrur V,
Campbell S, Wellen KE, Elenitoba-Johnson KSJ, Capell BC, Busino L.
FBXW7 Triggers Degradation of KMT2D to
Favor Growth of Diffuse Large B-cell
Lymphoma Cells. Cancer Res. 2020 Jun 15;80(12):2498–2511. PMCID:
PMC7417195
67.
Trinh DL, Scott DW, Morin RD, Mendez-Lago M, An
J, Jones SJM, Mungall AJ, Zhao Y, Schein J, Steidl C, Connors JM,
Gascoyne RD, Marra MA. Analysis of FOXO1 mutations in
diffuse large B-cell lymphoma. Blood.
2013;121(18):3666–3674. PMCID: PMC3643765
68.
Muppidi J, Schmitz R, Green JA, Green JA, Xiao
W, Larsen AB, Braun S, An J, Xu Y, Rosenwald A, Ott G, Gascoyne R,
Rimsza L, Campo E, Jaffe E, Delabie J, Smeland E, Braziel R, Tubbs R,
Cook J, Weisenburger D, Chan W, Vaidehi N, Staudt L, Cyster J. Loss of signaling via
Gα13 in germinal center B cell-derived
lymphoma. Nature. 2014;516:254–258.
69.
Pasqualucci L, Trifonov V, Fabbri G, Ma J,
Rossi D, Chiarenza A, Wells VA, Grunn A, Messina M, Elliot O, Chan J,
Bhagat G, Chadburn A, Gaidano G, Mullighan CG, Rabadan R, Dalla-Favera
R. Analysis of the coding genome of diffuse large B-cell lymphoma. Nat Genet. 2011 Jul
31;43(9):830–837. PMCID: PMC3297422
70.
Schmitz R, Wright GW, Huang DW, Johnson CA,
Phelan JD, Wang JQ, Roulland S, Kasbekar M, Young RM, Shaffer AL, Hodson
DJ, Xiao W, Yu X, Yang Y, Zhao H, Xu W, Liu X, Zhou B, Du W, Chan WC,
Jaffe ES, Gascoyne RD, Connors JM, Campo E, Lopez-Guillermo A, Rosenwald
A, Ott G, Delabie J, Rimsza LM, Tay Kuang Wei K, Zelenetz AD, Leonard
JP, Bartlett NL, Tran B, Shetty J, Zhao Y, Soppet DR, Pittaluga S,
Wilson WH, Staudt LM. Genetics and Pathogenesis of
Diffuse Large B-Cell Lymphoma. N Engl J Med. 2018 Apr
12;378(15):1396–1407. PMCID: PMC6010183
71.
Fangazio M, Ladewig E, Gomez K, Garcia-Ibanez
L, Kumar R, Teruya-Feldstein J, Rossi D, Filip I, Pan-Hammarström Q,
Inghirami G, Boldorini R, Ott G, Staiger AM, Chapuy B, Gaidano G, Bhagat
G, Basso K, Rabadan R, Pasqualucci L, Dalla-Favera R. Genetic mechanisms
of HLA-I loss and immune escape in diffuse large
B cell lymphoma. Proc Natl Acad Sci U S A. 2021 Jun
1;118(22):e2104504118. PMCID: PMC8179151
72.
Lazarian G, Yin S, Ten Hacken E, Sewastianik T,
Uduman M, Font-Tello A, Gohil SH, Li S, Kim E, Joyal H, Billington L,
Witten E, Zheng M, Huang T, Severgnini M, Lefebvre V, Rassenti LZ,
Gutierrez C, Georgopoulos K, Ott CJ, Wang L, Kipps TJ, Burger JA, Livak
KJ, Neuberg DS, Baran-Marszak F, Cymbalista F, Carrasco RD, Wu CJ. A
hotspot mutation in transcription factor IKZF3 drives
B cell neoplasia via transcriptional dysregulation. Cancer
Cell. 2021 Mar 8;39(3):380–393.e8. PMCID: PMC8034546
73.
Viganò E, Gunawardana J, Mottok A, Van Tol T,
Mak K, Chan FC, Chong L, Chavez E, Woolcock B, Takata K, Twa D, Shulha
HP, Telenius A, Kutovaya O, Hung SS, Healy S, Ben-Neriah S, Leroy K,
Gaulard P, Diepstra A, Kridel R, Savage KJ, Rimsza L, Gascoyne R, Steidl
C. Somatic
IL4R mutations in primary mediastinal large B-cell lymphoma lead to constitutive
JAK-STAT signaling activation. Blood. 2018 May
3;131(18):2036–2046.
74.
Qiu
Z, Khalife J, Ethiraj P, Jaafar C, Lin AP, Holder KN, Ritter JP, Chiou
L, Huelgas-Morales G, Aslam S, Zhang Z, Liu Z, Arya S, Gupta YK, Dahia
PLM, Aguiar RCT. IRF8-mutant B cell lymphoma
evades immunity through a CD74-dependent
deregulation of antigen processing and presentation in
MHCII complexes. Sci Adv. 2024 Jul 12;10(28):eadk2091.
PMCID: PMC11244530
75.
Tiacci E, Ladewig E, Schiavoni G, Penson A,
Fortini E, Pettirossi V, Wang Y, Rosseto A, Venanzi A, Vlasevska S,
Pacini R, Piattoni S, Tabarrini A, Pucciarini A, Bigerna B, Santi A,
Gianni AM, Viviani S, Cabras A, Ascani S, Crescenzi B, Mecucci C,
Pasqualucci L, Rabadan R, Falini B. Pervasive mutations of
JAK-STAT pathway genes in classical Hodgkin
lymphoma. Blood. 2018 May 31;131(22):2454–2465. PMCID: PMC6634958
76.
Choi J, Phelan JD, Wright GW, Häupl B, Huang
DW, Shaffer AL, Young RM, Wang Z, Zhao H, Yu X, Oellerich T, Staudt LM.
Regulation of B cell receptor-dependent NF-κB signaling by the tumor suppressor
KLHL14. Proc Natl Acad Sci U S A. 2020 Mar
17;117(11):6092–6102. PMCID: PMC7084139
77.
Choi J, Lee K, Ingvarsdottir K, Bonasio R,
Saraf A, Florens L, Washburn MP, Tadros S, Green MR, Busino L. Loss of
KLHL6 promotes diffuse large B-cell lymphoma growth and survival by stabilizing
the mRNA decay factor Roquin2. Nat Cell
Biol. 2018 May;20(5):586–596. PMCID: PMC5926793
78.
Ganapathi KA, Jobanputra V, Iwamoto F, Jain P,
Chen J, Cascione L, Nahum O, Levy B, Xie Y, Khattar P, Hoehn D, Bertoni
F, Murty VV, Pittaluga S, Jaffe ES, Alobeid B, Mansukhani MM, Bhagat G.
The genetic landscape
of dural marginal zone lymphomas. Oncotarget. Impact Journals; 2016
May 27;7(28):43052–43061.
79.
Zhang J, Jima D, Moffitt AB, Liu Q, Czader M,
Hsi ED, Fedoriw Y, Dunphy CH, Richards KL, Gill JI, Sun Z, Love C,
Scotland P, Lock E, Levy S, Hsu DS, Dunson D, Dave SS. The genomic
landscape of mantle cell lymphoma is related to the epigenetically
determined chromatin state of normal B cells. Blood.
2014 May 8;123(19):2988–2996.
80.
Zhou P, Blain AE, Newman AM, Zaka M, Chagaluka
G, Adlar FR, Offor UT, Broadbent C, Chaytor L, Whitehead A, Hall A,
O’Connor H, Van Noorden S, Lampert I, Bailey S, Molyneux E, Bacon CM,
Bomken S, Rand V. Sporadic and endemic Burkitt lymphoma
have frequent FOXO1 mutations but distinct hotspots in the
AKT recognition motif. Blood Adv. 2019 Jul
23;3(14):2118–2127. PMCID: PMC6650741
81.
Zhang J, Dominguez-Sola D, Hussein S, Lee JE,
Holmes AB, Bansal M, Vlasevska S, Mo T, Tang H, Basso K, Ge K,
Dalla-Favera R, Pasqualucci L. Disruption of KMT2D perturbs
germinal center B cell development and promotes
lymphomagenesis. Nat Med. 2015 Oct;21(10):1190–1198. PMCID: PMC5145002
82.
Scheffzek K, Ahmadian MR, Kabsch W, Wiesmüller
L, Lautwein A, Schmitz F, Wittinghofer A. The
Ras-RasGAP complex: Structural basis for
GTPase activation and its loss in oncogenic
Ras mutants. Science. 1997 Jul 18;277(5324):333–338.
83.
Pon
JR, Wong J, Saberi S, Alder O, Moksa M, Grace Cheng S-W, Morin GB,
Hoodless PA, Hirst M, Marra MA. MEF2B mutations in
non-Hodgkin lymphoma dysregulate cell migration by
decreasing MEF2B target gene activation. Nature
Communications [Internet]. 2015 Aug 6 [cited 2019 Dec 21];6(1):1–15.
Available from: https://www.nature.com/articles/ncomms8953
84.
De
Paoli L, Cerri M, Monti S, Rasi S, Spina V, Bruscaggin A, Greco M,
Ciardullo C, Famà R, Cresta S, Maffei R, Ladetto M, Martini M, Laurenti
L, Forconi F, Marasca R, Larocca LM, Bertoni F, Gaidano G, Rossi D. MGA, a
suppressor of MYC, is recurrently inactivated in high risk
chronic lymphocytic leukemia. Leuk Lymphoma. 2013
May;54(5):1087–1090.
85.
Kwanhian W, Lenze D, Alles J, Motsch N, Barth
S, Döll C, Imig J, Hummel M, Tinguely M, Trivedi P, Lulitanond V,
Meister G, Renner C, Grässer FA. MicroRNA-142 is mutated in
about 20% of diffuse large B-cell lymphoma.
Cancer Med. 2012 Oct;1(2):141–155. PMCID: PMC3544448
86.
Trissal MC, Wong TN, Yao JC, Ramaswamy R, Kuo
I, Baty J, Sun Y, Jih G, Parikh N, Berrien-Elliott MM, Fehniger TA, Ley
TJ, Maillard I, Reddy PR, Link DC. MIR142
Loss-of-Function Mutations Derepress ASH1L to Increase HOXA
Gene Expression and Promote Leukemogenesis. Cancer
Res. 2018 Jul 1;78(13):3510–3521. PMCID: PMC6030481
87.
Rushton CK, Arthur SE, Alcaide M, Cheung M,
Jiang A, Coyle KM, Cleary KLS, Thomas N, Hilton LK, Michaud N, Daigle S,
Davidson J, Bushell K, Yu S, Rys RN, Jain M, Shepherd L, Marra MA,
Kuruvilla J, Crump M, Mann K, Assouline S, Connors JM, Steidl C, Cragg
MS, Scott DW, Johnson NA, Morin RD. Genetic and evolutionary patterns of
treatment resistance in relapsed B-cell
lymphoma. Blood Adv. 2020 Jul 14;4(13):2886–2898. PMCID: PMC7362366
88.
Grabiner BC, Nardi V, Birsoy K, Possemato R,
Shen K, Sinha S, Jordan A, Beck AH, Sabatini DM. A diverse array of
cancer-associated MTOR mutations are hyperactivating and
can predict rapamycin sensitivity. Cancer Discov. 2014 May;4(5):554–563.
PMCID: PMC4012430
89.
Pasqualucci L, Neumeister P, Goossens T,
Nanjangud G, Chaganti RS, Küppers R, Dalla-Favera R. Hypermutation of multiple
proto-oncogenes in B-cell diffuse large-cell
lymphomas. Nature. 2001 Jul 19;412(6844):341–346.
90.
Freie B, Carroll PA, Varnum-Finney BJ, Ramsey
EL, Ramani V, Bernstein I, Eisenman RN. A germline point mutation in the
MYC-FBW7 phosphodegron initiates hematopoietic
malignancies. Genes Dev. 2024 Apr 17;38(5-6):253–272. PMCID: PMC11065175
91.
Johnston JM, Carroll WL. C-myc hypermutation in
Burkitt’s lymphoma. Leuk Lymphoma. 1992
Dec;8(6):431–439.
92.
Ngo
VN, Young RM, Schmitz R, Jhavar S, Xiao W, Lim KH, Kohlhammer H, Xu W,
Yang Y, Zhao H, Shaffer AL, Romesser P, Wright G, Powell J, Rosenwald A,
Muller-Hermelink HK, Ott G, Gascoyne RD, Connors JM, Rimsza LM, Campo E,
Jaffe ES, Delabie J, Smeland EB, Fisher RI, Braziel RM, Tubbs RR, Cook
JR, Weisenburger DD, Chan WC, Staudt LM. Oncogenically active
MYD88 mutations in human lymphoma. Nature. 2011 Feb
3;470(7332):115–119. PMCID: PMC5024568
93.
Thomas RK, Wickenhauser C, Tawadros S, Diehl V,
Küppers R, Wolf J, Schmitz R. Mutational
analysis of the IkappaBalpha gene in activated
B cell-like diffuse large B-cell lymphoma. Br J Haematol. 2004
Jul;126(1):50–54.
94.
Jungnickel B, Staratschek-Jox A, Bräuninger A,
Spieker T, Wolf J, Diehl V, Hansmann ML, Rajewsky K, Küppers R. Clonal
deleterious mutations in the IkappaBalpha gene in the
malignant cells in Hodgkin’s lymphoma. J Exp Med. 2000 Jan
17;191(2):395–402. PMCID: PMC2195754
95.
Morin RD, Assouline S, Alcaide M, Mohajeri A,
Johnston RL, Chong L, Grewal J, Yu S, Fornika D, Bushell K, Nielsen TH,
Petrogiannis-Haliotis T, Crump M, Tosikyan A, Grande BM, MacDonald D,
Rousseau C, Bayat M, Sesques P, Froment R, Albuquerque M, Monczak Y,
Oros KK, Greenwood C, Riazalhosseini Y, Arseneault M, Camlioglu E,
Constantin A, Pan-Hammarstrom Q, Peng R, Mann KK, Johnson NA. Genetic
Landscapes of Relapsed and Refractory
Diffuse Large B-Cell Lymphomas. Clin Cancer Res. 2016 May
1;22(9):2290–2300.
96.
Mansouri L, Sutton LA, Ljungström V, Bondza S,
Arngården L, Bhoi S, Larsson J, Cortese D, Kalushkova A, Plevova K,
Young E, Gunnarsson R, Falk-Sörqvist E, Lönn P, Muggen AF, Yan XJ,
Sander B, Enblad G, Smedby KE, Juliusson G, Belessi C, Rung J, Chiorazzi
N, Strefford JC, Langerak AW, Pospisilova S, Davi F, Hellström M,
Jernberg-Wiklund H, Ghia P, Söderberg O, Stamatopoulos K, Nilsson M,
Rosenquist R. Functional loss of IκBε leads to NF-κB deregulation in aggressive chronic
lymphocytic leukemia. J Exp Med. 2015 Jun 1;212(6):833–843. PMCID: PMC4451125
97.
Mansouri L, Noerenberg D, Young E, Mylonas E,
Abdulla M, Frick M, Asmar F, Ljungström V, Schneider M, Yoshida K,
Skaftason A, Pandzic T, Gonzalez B, Tasidou A, Waldhueter N,
Rivas-Delgado A, Angelopoulou M, Ziepert M, Arends CM, Couronné L, Lenze
D, Baldus CD, Bastard C, Okosun J, Fitzgibbon J, Dörken B, Drexler HG,
Roos-Weil D, Schmitt CA, Munch-Petersen HD, Zenz T, Hansmann ML,
Strefford JC, Enblad G, Bernard OA, Ralfkiaer E, Erlanson M,
Korkolopoulou P, Hultdin M, Papadaki T, Grønbæk K, Lopez-Guillermo A,
Ogawa S, Küppers R, Stamatopoulos K, Stavroyianni N, Kanellis G,
Rosenwald A, Campo E, Amini RM, Ott G, Vassilakopoulos TP, Hummel M,
Rosenquist R, Damm F. Frequent
NFKBIE deletions are associated with poor outcome in
primary mediastinal B-cell lymphoma.
Blood. 2016 Dec 8;128(23):2666–2670.
98.
Ryan RJH, Petrovic J, Rausch DM, Zhou Y, Lareau
CA, Kluk MJ, Christie AL, Lee WY, Tarjan DR, Guo B, Donohue LKH,
Gillespie SM, Nardi V, Hochberg EP, Blacklow SC, Weinstock DM, Faryabi
RB, Bernstein BE, Aster JC, Pear WS. A B Cell Regulome Links
Notch to Downstream Oncogenic Pathways in
Small B Cell Lymphomas. Cell Rep. 2017 Oct
17;21(3):784–797. PMCID: PMC5687286
99.
Lee
SY, Kumano K, Nakazaki K, Sanada M, Matsumoto A, Yamamoto G, Nannya Y,
Suzuki R, Ota S, Ota Y, Izutsu K, Sakata-Yanagimoto M, Hangaishi A,
Yagita H, Fukayama M, Seto M, Kurokawa M, Ogawa S, Chiba S.
Gain-of-function mutations and copy number increases of
Notch2 in diffuse large B-cell
lymphoma. Cancer Sci. 2009 May;100(5):920–926.
100.
Kuo HP, Ezell SA, Hsieh S, Schweighofer KJ,
Cheung LW, Wu S, Apatira M, Sirisawad M, Eckert K, Liang Y, Hsu J, Chen
CT, Beaupre D, Chang BY. The role of PIM1 in the
ibrutinib-resistant ABC subtype of diffuse large B-cell lymphoma. Am J Cancer Res.
2016;6(11):2489–2501. PMCID: PMC5126268
101.
González-Rincón J, Méndez M, Gómez S, García
JF, Martín P, Bellas C, Pedrosa L, Rodríguez-Pinilla SM, Camacho FI,
Quero C, Pérez-Callejo D, Rueda A, Llanos M, Gómez-Codina J, Piris MA,
Montes-Moreno S, Bárcena C, Rodríguez-Abreu D, Menárguez J, de la
Cruz-Merino L, Monsalvo S, Parejo C, Royuela A, Kwee I, Cascione L,
Arribas A, Bertoni F, Mollejo M, Provencio M, Sánchez-Beato M.
Unraveling transformation of follicular lymphoma to diffuse large B-cell lymphoma. PLoS One. 2019;14(2):e0212813.
PMCID: PMC6388933
102.
Hodson DJ, Shaffer AL, Xiao W, Wright GW,
Schmitz R, Phelan JD, Yang Y, Webster DE, Rui L, Kohlhammer H, Nakagawa
M, Waldmann TA, Staudt LM. Regulation of normal B-cell differentiation and malignant B-cell survival by OCT2. Proc Natl
Acad Sci U S A. 2016 Apr 5;113(14):E2039–2046. PMCID: PMC4833274
103.
Pasqualucci L, Compagno M, Houldsworth J, Monti
S, Grunn A, Nandula SV, Aster JC, Murty VV, Shipp MA, Dalla-Favera R.
Inactivation of the PRDM1/BLIMP1 gene in
diffuse large B cell lymphoma. J Exp Med. 2006
Feb;203(2):311–317.
104.
Pfeifer M, Grau M, Lenze D, Wenzel SS, Wolf A,
Wollert-Wulf B, Dietze K, Nogai H, Storek B, Madle H, Dörken B, Janz M,
Dirnhofer S, Lenz P, Hummel M, Tzankov A, Lenz G. PTEN loss
defines a PI3K/AKT pathway-dependent germinal
center subtype of diffuse large B-cell
lymphoma. Proc Natl Acad Sci U S A. 2013 Jul 23;110(30):12420–12425.
PMCID: PMC3725065
105.
Demosthenous C, Han JJ, Hu G, Stenson M, Gupta
M. Loss of function mutations in PTPN6 promote
STAT3 deregulation via JAK3 kinase in diffuse
large B-cell lymphoma. Oncotarget. 2015 Dec
29;6(42):44703–44713. PMCID: PMC4792586
106.
Pinyol M, Bea S, Plà L, Ribrag V, Bosq J,
Rosenwald A, Campo E, Jares P. Inactivation of
RB1 in mantle-cell lymphoma detected by nonsense-mediated
mRNA decay pathway inhibition and microarray
analysis. Blood. 2007 Jun 15;109(12):5422–5429.
107.
Weber J, de la Rosa J, Grove CS, Schick M, Rad
L, Baranov O, Strong A, Pfaus A, Friedrich MJ, Engleitner T, Lersch R,
Öllinger R, Grau M, Menendez IG, Martella M, Kohlhofer U, Banerjee R,
Turchaninova MA, Scherger A, Hoffman GJ, Hess J, Kuhn LB, Ammon T, Kim
J, Schneider G, Unger K, Zimber-Strobl U, Heikenwälder M,
Schmidt-Supprian M, Yang F, Saur D, Liu P, Steiger K, Chudakov DM, Lenz
G, Quintanilla-Martinez L, Keller U, Vassiliou GS, Cadiñanos J, Bradley
A, Rad R. PiggyBac transposon tools for recessive screening
identify B-cell lymphoma drivers in mice.
Nat Commun. 2019 Mar 29;10(1):1415. PMCID: PMC6440946
108.
O’Hayre M, Inoue A, Kufareva I, Wang Z, Mikelis
CM, Drummond RA, Avino S, Finkel K, Kalim KW, DiPasquale G, Guo F, Aoki
J, Zheng Y, Lionakis MS, Molinolo AA, Gutkind JS. Inactivating mutations
in GNA13 and RHOA in Burkitt’s
lymphoma and diffuse large B-cell lymphoma:
A tumor suppressor function for the Gα13/RhoA
axis in B cells. Oncogene. 2016 Jul 21;35(29):3771–3780.
PMCID: PMC4885800
109.
Okosun J, Wolfson RL, Wang J, Araf S, Wilkins
L, Castellano BM, Escudero-Ibarz L, Al Seraihi AF, Richter J, Bernhart
SH, Efeyan A, Iqbal S, Matthews J, Clear A, Guerra-Assunção JA, Bödör C,
Quentmeier H, Mansbridge C, Johnson P, Davies A, Strefford JC, Packham
G, Barrans S, Jack A, Du MQ, Calaminici M, Lister TA, Auer R, Montoto S,
Gribben JG, Siebert R, Chelala C, Zoncu R, Sabatini DM, Fitzgibbon J.
Recurrent mTORC1-activating RRAGC mutations
in follicular lymphoma. Nat Genet. 2016 Feb;48(2):183–188. PMCID: PMC4731318
110.
Cazzola M, Rossi M, Malcovati L, Associazione
Italiana per la Ricerca sul Cancro Gruppo Italiano Malattie
Mieloproliferative. Biologic and clinical significance of somatic
mutations of SF3B1 in myeloid and lymphoid neoplasms.
Blood. 2013 Jan 10;121(2):260–269. PMCID: PMC3790951
111.
Gao J, Sidiropoulou E, Walker I, Krupka JA,
Mizielinski K, Usheva Z, Samarajiwa SA, Hodson DJ. SGK1
mutations in DLBCL generate hyperstable protein neoisoforms
that promote AKT independence. Blood. 2021 Sep
16;138(11):959–964. PMCID: PMC8701626
112.
Fernando TM, Piskol R, Bainer R, Sokol ES,
Trabucco SE, Zhang Q, Trinh H, Maund S, Kschonsak M, Chaudhuri S,
Modrusan Z, Januario T, Yauch RL. Functional characterization of
SMARCA4 variants identified by targeted exome-sequencing of
131,668 cancer patients. Nat Commun. 2020 Nov 3;11(1):5551. PMCID: PMC7609548
113.
Nadeu F, Martín-García D, Clot G, Díaz-Navarro
A, Duran-Ferrer M, Navarro A, Vilarrasa-Blasi R, Kulis M, Royo R,
Gutiérrez-Abril J, Valdés-Mas R, López C, Chapaprieta V, Puiggrós M,
Castellano G, Costa D, Aymerich M, Jares P, Espinet B, Muntañola A,
Ribera‐Cortada I, Siebert R, Colomer D, Torrents D, Giné E,
López-Guillermo A, Küppers R, Martín-Subero J, Puente X, Beà S, Campo E.
Genomic and
epigenomic insights into the origin, pathogenesis and clinical behavior
of mantle cell lymphoma subtypes. Blood. 2020;
114.
Melzner I, Bucur AJ, Brüderlein S, Dorsch K,
Hasel C, Barth TFE, Leithäuser F, Möller P. Biallelic mutation of
SOCS-1 impairs JAK2 degradation and sustains
phospho-JAK2 action in the MedB-1 mediastinal
lymphoma line. Blood. 2005 Mar 15;105(6):2535–2542.
115.
Weniger MA, Melzner I, Menz CK, Wegener S,
Bucur AJ, Dorsch K, Mattfeldt T, Barth TFE, Möller P. Mutations of the tumor
suppressor gene SOCS-1 in classical Hodgkin
lymphoma are frequent and associated with nuclear
phospho-STAT5 accumulation. Oncogene. 2006 Apr
27;25(18):2679–2684.
116.
Hu
G, Witzig TE, Gupta M. A novel missense (M206K)
STAT3 mutation in diffuse large B cell
lymphoma deregulates STAT3 signaling. PLoS One.
2013;8(7):e67851. PMCID: PMC3701620
117.
Yildiz M, Li H, Bernard D, Amin NA, Ouillette
P, Jones S, Saiya-Cork K, Parkin B, Jacobi K, Shedden K, Wang S, Chang
AE, Kaminski MS, Malek SN. Activating STAT6 mutations in
follicular lymphoma. Blood. 2015 Jan 22;125(4):668–679. PMCID: PMC4729538
118.
Mentz M, Keay W, Strobl CD, Antoniolli M,
Adolph L, Heide M, Lechner A, Haebe S, Osterode E, Kridel R, Ziegenhain
C, Wange LE, Hildebrand JA, Shree T, Silkenstedt E, Staiger AM, Ott G,
Horn H, Szczepanowski M, Richter J, Levy R, Rosenwald A, Enard W,
Zimber-Strobl U, von Bergwelt-Baildon M, Hiddemann W, Klapper W,
Schmidt-Supprian M, Rudelius M, Bararia D, Passerini V, Weigert O.
PARP14 is a novel target in STAT6 mutant
follicular lymphoma. Leukemia. 2022 Sep;36(9):2281–2292. PMCID: PMC9417990
119.
Ritz O, Guiter C, Castellano F, Dorsch K,
Melzner J, Jais JP, Dubois G, Gaulard P, Möller P, Leroy K. Recurrent
mutations of the STAT6 DNA binding domain in primary
mediastinal B-cell lymphoma. Blood. 2009 Aug
6;114(6):1236–1242. PMCID: PMC2824656
120.
Venturutti L, Teater M, Zhai A, Chadburn A,
Babiker L, Kim D, Béguelin W, Lee TC, Kim Y, Chin CR, Yewdell WT, Raught
B, Phillip JM, Jiang Y, Staudt LM, Green MR, Chaudhuri J, Elemento O,
Farinha P, Weng AP, Nissen MD, Steidl C, Morin RD, Scott DW, Privé GG,
Melnick AM. TBL1XR1 Mutations Drive Extranodal Lymphoma by
Inducing a Pro-tumorigenic Memory
Fate. Cell. 2020 Jul 23;182(2):297–316.e27. PMCID: PMC7384961
121.
Asmar F, Punj V, Christensen J, Pedersen MT,
Pedersen A, Nielsen AB, Hother C, Ralfkiaer U, Brown P, Ralfkiaer E,
Helin K, Grønbæk K. Genome-wide profiling identifies a DNA
methylation signature that associates with TET2 mutations
in diffuse large B-cell lymphoma.
Haematologica. 2013 Dec;98(12):1912–1920. PMCID: PMC3856967
122.
Ennishi D, Healy S, Bashashati A, Saberi S,
Hother C, Mottok A, Chan FC, Chong L, Abraham L, Kridel R, Boyle M,
Meissner B, Aoki T, Takata K, Woolcock BW, Viganò E, Gold M, Molday LL,
Molday RS, Telenius A, Li MY, Wretham N, Dos Santos N, Wong M, Viller
NN, Uger RA, Duns G, Baticados A, Madero A, Bristow BN, Farinha P, Slack
GW, Ben-Neriah S, Lai D, Zhang AW, Salehi S, Shulha HP, Chiu DS,
Mostafavi S, Gerrie AS, Huang DW, Rushton C, Villa D, Sehn LH, Savage
KJ, Mungall AJ, Weng AP, Bally MB, Morin RD, Cohen Freue GV, Staudt LM,
Connors JM, Marra MA, Shah SP, Gascoyne RD, Scott DW, Steidl C.
TMEM30A loss-of-function mutations drive lymphomagenesis
and confer therapeutically exploitable vulnerability in B-cell lymphoma. Nat Med. 2020 Apr;26(4):577–588.
PMCID: PMC8480332
123.
Compagno M, Lim WK, Grunn A, Nandula SV,
Brahmachary M, Shen Q, Bertoni F, Ponzoni M, Scandurra M, Califano A,
Bhagat G, Chadburn A, Dalla-Favera R, Pasqualucci L. Mutations of
multiple genes cause deregulation of NF-kappaB in diffuse large B-cell lymphoma. Nature. 2009 Jun
4;459(7247):717–721. PMCID: PMC2973325
124.
Rossi D, Deaglio S, Dominguez-Sola D, Rasi S,
Vaisitti T, Agostinelli C, Spina V, Bruscaggin A, Monti S, Cerri M,
Cresta S, Fangazio M, Arcaini L, Lucioni M, Marasca R, Thieblemont C,
Capello D, Facchetti F, Kwee I, Pileri SA, Foà R, Bertoni F,
Dalla-Favera R, Pasqualucci L, Gaidano G. Alteration of
BIRC3 and multiple other NF-κB
pathway genes in splenic marginal zone lymphoma. Blood. 2011 Nov
3;118(18):4930–4934.
125.
Schmitz R, Hansmann ML, Bohle V, Martin-Subero
JI, Hartmann S, Mechtersheimer G, Klapper W, Vater I, Giefing M, Gesk S,
Stanelle J, Siebert R, Küppers R. TNFAIP3
(A20) is a tumor suppressor gene in Hodgkin
lymphoma and primary mediastinal B cell lymphoma. J Exp
Med. 2009 May 11;206(5):981–989. PMCID: PMC2715030
126.
Cheung KJJ, Johnson NA, Affleck JG, Severson T,
Steidl C, Ben-Neriah S, Schein J, Morin RD, Moore R, Shah SP, Qian H,
Paul JE, Telenius A, Relander T, Lam W, Savage K, Connors JM, Brown C,
Marra MA, Gascoyne RD, Horsman DE. Acquired
TNFRSF14 mutations in follicular lymphoma are associated
with worse prognosis. Cancer Res. 2010 Nov 15;70(22):9166–9174.
127.
Kato S, Han SY, Liu W, Otsuka K, Shibata H,
Kanamaru R, Ishioka C. Understanding the function-structure and
function-mutation relationships of P53 tumor suppressor protein by
high-resolution missense mutation analysis. Proc Natl Acad Sci U S A.
2003 Jul 8;100(14):8424–8429. PMCID: PMC166245
128.
Wilda M, Bruch J, Harder L, Rawer D, Reiter A,
Borkhardt A, Woessmann W. Inactivation of the ARF-MDM-2-p53 pathway in sporadic
Burkitt’s lymphoma in children. Leukemia. 2004
Mar;18(3):584–588.
129.
Mareschal S, Dubois S, Viailly PJ, Bertrand P,
Bohers E, Maingonnat C, Jaïs JP, Tesson B, Ruminy P, Peyrouze P,
Copie-Bergman C, Fest T, Jo Molina T, Haioun C, Salles G, Tilly H,
Lecroq T, Leroy K, Jardin F. Whole exome sequencing of
relapsed/refractory patients expands the repertoire of somatic mutations
in diffuse large B-cell lymphoma. Genes
Chromosomes Cancer. 2016 Mar;55(3):251–267.
130.
Miloudi H, Bohers É, Guillonneau F, Taly A,
Gibouin VC, Viailly PJ, Jego G, Grumolato L, Jardin F, Sola B.
XPO1E571K Mutation Modifies Exportin 1
Localisation and Interactome in B-cell Lymphoma. Cancers (Basel). 2020 Sep
30;12(10):2829. PMCID: PMC7600770
131.
Jardin F, Pujals A, Pelletier L, Bohers E,
Camus V, Mareschal S, Dubois S, Sola B, Ochmann M, Lemonnier F, Viailly
PJ, Bertrand P, Maingonnat C, Traverse-Glehen A, Gaulard P, Damotte D,
Delarue R, Haioun C, Argueta C, Landesman Y, Salles G, Jais JP, Figeac
M, Copie-Bergman C, Molina TJ, Picquenot JM, Cornic M, Fest T, Milpied
N, Lemasle E, Stamatoullas A, Moeller P, Dyer MJS, Sundstrom C, Bastard
C, Tilly H, Leroy K. Recurrent mutations of the
exportin 1 gene (XPO1) and their impact on selective
inhibitor of nuclear export compounds sensitivity in primary mediastinal
B-cell lymphoma. Am J Hematol. 2016
Sep;91(9):923–930.
132.
Skalniak L, Mizgalska D, Zarebski A,
Wyrzykowska P, Koj A, Jura J. Regulatory
feedback loop between NF-kappaB and MCP-1-induced protein 1 RNase.
FEBS J. 2009 Oct;276(20):5892–5905.
133.
Shin SY, Lee ST, Kim HJ, Ki CS, Jung CW, Kim
JW, Kim SH. BRAF V600E and MAP2K1 mutations in
hairy cell leukemia and splenic marginal zone lymphoma cases. Ann Lab
Med. 2015 Mar;35(2):257–259. PMCID: PMC4330180
134.
Louissaint A, Schafernak KT, Geyer JT, Kovach
AE, Ghandi M, Gratzinger D, Roth CG, Paxton CN, Kim S, Namgyal C, Morin
R, Morgan EA, Neuberg DS, South ST, Harris MH, Hasserjian RP, Hochberg
EP, Garraway LA, Harris NL, Weinstock DM. Pediatric-type nodal
follicular lymphoma: A biologically distinct lymphoma with frequent
MAPK pathway mutations. Blood. 2016 Aug
25;128(8):1093–1100. PMCID: PMC5000844
135.
Otto C, Giefing M, Massow A, Vater I, Gesk S,
Schlesner M, Richter J, Klapper W, Hansmann ML, Siebert R, Küppers R. Genetic lesions
of the TRAF3 and MAP3K14 genes in classical
Hodgkin lymphoma. Br J Haematol. 2012
Jun;157(6):702–708.
136.
Abate F, Ambrosio M, Mundo L, Laginestra M,
Fuligni F, Rossi M, Zairis S, Gazaneo S, Falco GD, Lazzi S, Bellan C,
Rocca BJ, Amato T, Marasco E, Etebari M, Ogwang M, Calbi V, Ndede I,
Patel K, Chumba D, Piccaluga P, Pileri S, Leoncini L, Rabadán R. Distinct
Viral and Mutational Spectrum of Endemic
Burkitt Lymphoma. PLoS Pathogens. 2015;11.


