4.5 Article

MicroRNA-145 is a potential prognostic factor of scirrhous type gastric cancer

期刊

ONCOLOGY REPORTS
卷 32, 期 4, 页码 1720-1726

出版社

SPANDIDOS PUBL LTD
DOI: 10.3892/or.2014.3333

关键词

alpha-smooth muscle actin; fibroblast; microRNA-145; scirrhous type gastric cancer; transforming growth factor-beta

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资金

  1. Ministry of Education, Culture, Science, Sports, and Technology of Japan
  2. Ministry of Health, Labour and Welfare of Japan
  3. Japan Society for the Promotion of Science
  4. National Cancer Center Research and Development Fund [23-A-9]
  5. Grants-in-Aid for Scientific Research [25460417] Funding Source: KAKEN

向作者/读者索取更多资源

Gastric cancer (GC) is one of the most common malignancies worldwide. In particular, scirrhous type GC is highly metastatic and is characterized clinically by rapid disease progression and poor prognosis. MicroRNAs (miRNAs) play crucial roles in cancer development and progression. We previously demonstrated by microarray analysis that microRNA-145 (miR-145) is one of the more highly expressed miRNAs in scirrhous type GC vs. non-scirrhous types of GC. In the present study, we investigated the role of miR-145 in scirrhous type GC. The expression levels of miR-145 assessed by quantitative RT-PCR were higher in scirrhous type GC tissue samples than in non-scirrhous type GC and corresponding normal tissues. GC patients with high miR-145 expression were at a more advanced tumor stage (P=0.0156) and had more scirrhous type histology (P=0.0054) than those with low miR-145 expression. Furthermore, miR-145 expression was significantly associated with poor prognosis in GC patients (P=0.0438). miR-145 expression was localized in stromal fibroblasts of scirrhous type GC but not in cancer cells. miR-145 was induced by treatment by transforming growth factor-beta, and it enhanced the expression of a-smooth muscle actin, a marker of myofibroblasts, in both normal gastric fibroblasts and cancer-associated fibroblasts. These data suggest that miR-145 may contribute to the progression of scirrhous type GC by regulating activation of peri-tumoral fibroblasts.

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