z-logo
Premium
Micro RNA ‐378 inhibits cell growth and enhances l ‐ OHP ‐induced apoptosis in human colorectal cancer
Author(s) -
Wang KaiYu,
Ma Jun,
Zhang FuXi,
Yu MingJun,
Xue JiShan,
Zhao JiSheng
Publication year - 2014
Publication title -
iubmb life
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.132
H-Index - 113
eISSN - 1521-6551
pISSN - 1521-6543
DOI - 10.1002/iub.1317
Subject(s) - apoptosis , chemistry , cell growth , rna , microbiology and biotechnology , biology , biochemistry , gene
MicroRNAs (miRNAs) are small noncoding RNAs that participate in a variety of biological processes, and dysregulation of miRNAs is widely associated with cancer development and progression. MiR‐378 is frequently downregulated in colorectal cancer (CRC) and colorectal cell lines; however, it has high serum levels. Bioinformatics analysis further deduced that CDC40 is a potential target of miR‐378, and luciferase reporter assays confirmed the direct regulation of CDC40 by miR‐378. CDC40 plays a key role in cell cycle progression through G1/S and G2/M and pre‐mRNA splicing. Subsequently, we determined that miR‐378 inhibits cell growth and the G1/S transition in CRC cells and that these effects were CDC40‐dependent. Finally, miR‐378 increased cell apoptosis induced by the chemotherapeutic drug l ‐OHP. Our data highlight the potential application of miR‐378 as a tumor suppressor for CRC therapy and overcoming chemoresistance, and it may also be a potential tumor marker for CRC prognosis. © 2014 IUBMB Life, 66(9):645–654, 2014

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom