SRPX2 regulates colon cancer cell metabolism by miR-192/215 via PI3K-Akt

被引：9

作者：

Zhao, Jian ^{[1
]}

Xu, Jian ^{[1
]}

Zhang, Rui ^{[1
]}

机构：

[1] China Med Univ, Liaoning Canc Hosp & Inst, Canc Hosp, Dept Colorectal Surg, 44 Xiaoheyan Rd, Shenyang 110042, Liaoning, Peoples R China

来源：

AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2018年 / 10卷 / 02期

关键词：

SRPX2; miR-192; miR-215; colon cancer; PI3K-Akt; GASTRIC-CANCER; COLORECTAL-CANCER; MICRORNA-192; SUPPRESSES; MIR-215; GLIOBLASTOMA; PROGRESSION; METASTASIS; EXPRESSION; DISORDERS; PROGNOSIS;

D O I：

暂无

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

Colon cancer is one of common cancer in the world and glycolysis is one of the major problems in colon cancer therapy. MicroRNAs (miRNAs) involve in colon cancer progression. Sushi repeat-containing protein X-linked 2 (SRPX2) is associated with poor prognosis in some cancer patients, however, the role of SRPX2 including glycolytic metabolism regulated by miRNAs is unclear in colon cancer. So, the purpose of the present study is to elucidate the underlying mechanism in colon cancer metabolism mediated by SRPX2. Our results revealed that miR-192-5p (miR-192) and miR-215-5p (miR-215) inhibited glycolysis by regulating SRPX2 expression in colon cancer cells. We also found that miR-192 and miR-215 were both regulated by PI3K-Akt. Our results indicate that SRPX2 facilitates colon cancer cell glycolysis by miR-192 and miR-215, which are down-regulated by PI3K-Akt.

引用

页码：483 / 490

页数：8

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