4.6 Article

Overexpression of Circular RNA ciRS-7 Abrogates the Tumor Suppressive Effect of miR-7 on Gastric Cancer via PTEN/PI3K/AKT Signaling Pathway

期刊

JOURNAL OF CELLULAR BIOCHEMISTRY
卷 119, 期 1, 页码 440-446

出版社

WILEY
DOI: 10.1002/jcb.26201

关键词

GASTRIC CANCER (GC); CIRCULAR RNA; ciRS-7; miR-7; miRNA; OVERALL SURVIVAL (OS)

资金

  1. Natural Science Foundation of China [81402771]
  2. Science and Technology Development Foundation of Dongguan City [2013108101056]
  3. Science and Technology Key Project Foundation of Zhanjiang City [2014B01020]
  4. Guangdong High-level Personnel of Special Support Program for Outstanding Young Teachers [YQ201401]

向作者/读者索取更多资源

Gastric cancer (GC) has one of the highest mortality rates of malignancies globally. Currently, ciRS-7, a novel circular RNA, has emerged as a potential sponge for miR-7. However, few studies on ciRS-7 in GC have been performed. In this study, we investigated the clinical significance and function of ciRS-7 in GC. First, the expression levels of ciRS-7 in 102 primary GC tissues and the matched para-carcinoma tissues were evaluated and the clinical relevance was confirmed in an independent validation cohort (n=154). Second, the effects of ciRS-7 on miR-7, PTEN, and PI3K were evaluated. Finally, the function of ciRS-7 in GC was analyzed with cell lines and nude mice. The expression of ciRS-7 was significantly upregulated in GC tissues compared with the matched para-carcinoma tissues (P=0.0023), and the upregulation of ciRS-7 was linked to poor survival in the testing (P=0.0143) and validation cohort (P=0.0061). Multivariate survival analysis revealed that ciRS-7 was probably an independent risk factor of overall survival (P<0.05). Furthermore, overexpression of ciRS-7 blocked the miR-7-induced tumor suppression in MGC-803 and HGC-27 cells and led to a more aggressive oncogenic phenotype, via antagonizing miR-7-mediated PTEN/PI3K/AKT pathway. ciRS-7 may act as a prospective prognostic biological marker and a promising therapeutic target for GC. J. Cell. Biochem. 119: 440-446, 2018. (c) 2017 Wiley Periodicals, Inc.

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