Table of Contents
Experimental Evidence
Driver mutations affecting this gene in DLBCL have been experimentally demonstrated to cause a reduction or loss of function (LOF).1
Relevance tier by entity
| Entity | Tier | Description |
|---|---|---|
| 2 | Role of MIR142 mutations in BL requires confirmation | |
| 1 | High-confidence DLBCL gene |
Mutation incidence in large patient cohorts (GAMBL reanalysis)
| pathology | Collection | N | mutated | Incidence | CI |
|---|---|---|---|---|---|
| BL | GAMBL without Panea | 309 | 0 | 0 | [0,0] |
| BL | GAMBL without ICGC/Zhou | 320 | 0 | 0 | [0,0] |
| BL | GAMBL with Panea | 410 | 0 | 0 | [0,0] |
| BL | BLGSP | 219 | 0 | 0 | [0,0] |
| BL | Zhou/ICGC | 90 | 0 | 0 | [0,0] |
| BL | Panea | 101 | 0 | 0 | [0,0] |
MIR142 Expression
History
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timeline
title Publication timing
2012-10-1 : Kwanhian : DLBCL
2019-03-21 : Grande : BL
References
1.
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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
2.
Grande BM, Gerhard DS, Jiang A, Griner NB,
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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
3.
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


