| Literature DB >> 26455548 |
Faeza Ebrahimi1, Vinod Gopalan2, Riajul Wahab1, Cu-Tai Lu3, Robert Anthony Smith4, Alfred King-Yin Lam5.
Abstract
In this study, we investigated the expression profiles and clinicopathological significance of miR-126 in large cohort of patients with colorectal cancers as well the cellular repercussions of miR-126 in colon cancer cells along with its targets in-vitro. Down regulation of miR-126 expression was associated with histological subtypes, peri-neural tumour infiltration, microsatellite instability and pathological staging of colorectal cancers (p<0.05). Low miR-126 expression was also associated with poorer survival in patients with colorectal cancer. Analysis of matched tissues from the same patient revealed that approximately 70% of the tested patients had similar levels of expression of miR-126 in primary cancer and cancer metastases in both lymph node and distant metastases. In addition, induced overexpression of miR-126 showed reduced cell proliferation, increased apoptosis and decreased accumulation of cells in the G0-G1 phase of the colon cancer cells. Furthermore, SW480(+miR-126) cells showed reduced BCL-2 and increased P53 protein expression. To conclude, deregulation of miR-126 in colorectal cancer at the tissue and cellular levels as well as its correlation with various clinicopathological parameters confirm the cancer suppressive role of miR-126 in colorectal cancer.Entities:
Keywords: Apoptosis; Colorectal cancer; Down regulation; Metastasis; MiR-126
Mesh:
Substances:
Year: 2015 PMID: 26455548 DOI: 10.1016/j.yexcr.2015.10.004
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905