| Literature DB >> 24969300 |
Li Ying Liu1, Wei Wang2, Lin Yu Zhao3, Bo Guo3, Juan Yang3, Xiao Ge Zhao1, Ni Hou3, Lei Ni3, Ai Ying Wang3, Tu Sheng Song3, Chen Huang1, Ji Ru Xu4.
Abstract
MicroRNA (miRNA)-126 (miR-126) was reported to be downregulated and to act as a tumor suppressor in cancers of the lung, cervix, bladder and prostate. However, the functions of miR-126 in gastric cancer appear to be diverse and are largely unknown. MiR-126 was reported to act as a tumor suppressor by targeting the Crk gene, or as an oncogene by targeting the SOX2 gene in gastric cancer. We identified that the expression of miR-126 was decreased in gastric cancer cell lines and tissues. PLK2, a tumor suppressor gene, was directly regulated by miR-126 in SGC-7901 cells. Overexpression of miR-126 not only suppressed the growth and clone formation of SGC-7901 cells, but also induced apoptosis in vitro, whereas inhibition of miR-126 slightly promoted SGC-7901 cell proliferation. The cell cycle was not affected by miR-126. Moreover, miR-126 suppressed tumor growth in vivo in a xenograft model. PLK2, PI3KR2 and Crk were regulated by miR-126 in SGC-7901 cells. We infer that the functions of miR-126 in gastric cancer depend on synergistic targeting balance between oncogenes and anti-oncogenes. Our study indicates that miR-126 is a tumor suppressor, which in the future may become a therapeutic target for gastric cancer.Entities:
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Year: 2014 PMID: 24969300 DOI: 10.3892/ijo.2014.2516
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650