Dual mechanisms by which miR-125b represses IRF4 to induce myeloid and B-cell leukemias

Author:

So Alex Yick-Lun1,Sookram Reeshelle1,Chaudhuri Aadel A.12,Minisandram Aarathi1,Cheng David1,Xie Catherine1,Lim Ee Lyn1,Flores Yvette Garcia1,Jiang Shuai1,Kim Jocelyn Tammy1,Keown Christopher3,Ramakrishnan Parameswaran4,Baltimore David1

Affiliation:

1. Department of Biology, California Institute of Technology, Pasadena, CA;

2. Department of Radiation Oncology, Stanford University School of Medicine, Stanford, CA;

3. Department of Cognitive Science, University of California San Diego, La Jolla, CA; and

4. Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH

Abstract

Key Points MiR-125b induces tumorigenesis in myeloid cells by repressing the expression of IRF4 at the mRNA and protein level. MiR-125b promotes oncogenesis in B cells that involves selection of cells that acquire genetic deletion of the gene encoding IRF4.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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