| Literature DB >> 26719093 |
Haiyang Zhang1, Yanjun Qu1, Jingjing Duan1, Ting Deng1, Rui Liu1, Le Zhang1, Ming Bai1, Jialu Li2, Likun Zhou1, Tao Ning1, Hongli Li1, Shaohua Ge1, Hua Li1, Guoguang Ying1, Dingzhi Huang1, Yi Ba1.
Abstract
Gastric cancer is one of the most common malignant tumors worldwide; however, the efficacy of clinical treatment is limited. MicroRNAs (miRNAs) are a class of small non-coding RNAs that have been reported to play a key role in the development of cancer. They also provide novel candidates for targeted therapy. To date, in-depth studies on the molecular mechanisms of gastric cancer involving miRNAs are still absent. We previously reported that 5 miRNAs were identified as being significantly increased in gastric cancer, and the role of these miRNAs was investigated in the present study. By using bioinformatics tools, we found that more than 4,000 unique genes are potential downstream targets of gastric cancer miRNAs, and these targets belong to the protein class of nucleic acid binding, transcription factor, enzyme modulator, transferase and receptor. Pathway mapping showed that the targets of gastric cancer miRNAs are involved in the MAPK signaling pathway, pathways in cancer, the PI3K-Akt signaling pathway, the HTLV-1 signaling pathway and Ras signaling pathway, thus regulating cell growth, differentiation, apoptosis and metastasis. Analysis of the pathways related to miRNAs may provides potential drug targets for future therapy of gastric cancer.Entities:
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Year: 2015 PMID: 26719093 DOI: 10.3892/or.2015.4451
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906