A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL). Academic Article uri icon

Overview

abstract

  • The importance of individual microRNAs (miRNAs) has been established in specific cancers. However, a comprehensive analysis of the contribution of miRNAs to the pathogenesis of any specific cancer is lacking. Here we show that in T-cell acute lymphoblastic leukemia (T-ALL), a small set of miRNAs is responsible for the cooperative suppression of several tumor suppressor genes. Cross-comparison of miRNA expression profiles in human T-ALL with the results of an unbiased miRNA library screen allowed us to identify five miRNAs (miR-19b, miR-20a, miR-26a, miR-92 and miR-223) that are capable of promoting T-ALL development in a mouse model and which account for the majority of miRNA expression in human T-ALL. Moreover, these miRNAs produce overlapping and cooperative effects on tumor suppressor genes implicated in the pathogenesis of T-ALL, including IKAROS (also known as IKZF1), PTEN, BIM, PHF6, NF1 and FBXW7. Thus, a comprehensive and unbiased analysis of miRNA action in T-ALL reveals a striking pattern of miRNA-tumor suppressor gene interactions in this cancer.

publication date

  • June 5, 2011

Research

keywords

  • Gene Regulatory Networks
  • Genes, Tumor Suppressor
  • MicroRNAs
  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Identity

PubMed Central ID

  • PMC4121855

Scopus Document Identifier

  • 79959714872

Digital Object Identifier (DOI)

  • 10.1038/ng.858

PubMed ID

  • 21642990

Additional Document Info

volume

  • 43

issue

  • 7