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A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL).
- Source :
-
Nature genetics [Nat Genet] 2011 Jun 05; Vol. 43 (7), pp. 673-8. Date of Electronic Publication: 2011 Jun 05. - Publication Year :
- 2011
-
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.
- Subjects :
- Adolescent
Adult
Animals
Apoptosis
Biomarkers, Tumor genetics
Blotting, Western
Cell Line, Tumor
Cell Proliferation
Child
Child, Preschool
Female
Fluorescent Antibody Technique
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Humans
Immunoenzyme Techniques
Infant
Luciferases metabolism
Male
Mice
MicroRNAs metabolism
Oligonucleotide Array Sequence Analysis
RNA, Messenger genetics
Reverse Transcriptase Polymerase Chain Reaction
Survival Rate
Young Adult
Gene Regulatory Networks
Genes, Tumor Suppressor
MicroRNAs genetics
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1546-1718
- Volume :
- 43
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Nature genetics
- Publication Type :
- Academic Journal
- Accession number :
- 21642990
- Full Text :
- https://doi.org/10.1038/ng.858