miR-659-3p is involved in the regulation of the chemotherapy response of colorectal cancer via modulating the expression of SPHK1

被引:1
|
作者
Li, Shuyuan [1 ]
Fang, Ying [2 ]
Qin, Hai [1 ]
Fu, Wenzheng [1 ]
Zhang, Xipeng [1 ]
机构
[1] Tianjin Union Med Ctr, Dept Colorectal Surg, 190 Jieyuan Rd, Tianjin 300121, Peoples R China
[2] First Hosp Jiaxing, Dept Pathol, Jiaxing 314000, Zhejiang, Peoples R China
来源
AMERICAN JOURNAL OF CANCER RESEARCH | 2016年 / 6卷 / 09期
关键词
miR-659-3p; SPHK1; colorectal cancer; CRC; CDDP; cisplatin; SPHINGOSINE KINASE 1; TARGETING SPHK1; CELL-PROLIFERATION; SIGNALING PATHWAY; BREAST-CANCER; MIGRATION; INVASION; STATISTICS; THERAPY; DISEASE;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) is one of most prevalent malignant diseases worldwide. Metastasis and chemoresistance are the two prominent death-related factors of CRCs. Thus, it is urgent to understand the mechanism responsible for the chemo-resistant properties of CRC and develop new therapeutic methods. Here, we found that the expression of miR-659-3p was significantly reduced in cisplatin (CDDP)-resistant HT29 and LOVO colorectal cancer cells and in CDDP-resistant clinical colorectal cancer samples compared with respective CDDP-sensitive counterparts. Sphingosine kinase 1 (SPHK1) is a direct target of miR-659-3p in colorectal cancer cells, and it is negatively regulated by miR-659-3p. We found that anti-miR-659-3p could increase the IC50 of CDDP in parental HT29 and LOVO colorectal cancer cells; additionally, miR-659-3p mimics decreased the IC50 of CDDP in HT29/CDDP and LOVO/CDDP colorectal cancer cells. Furthermore, we showed that the miR-659-3p/SPHK1 pathway was involved in the regulation of chemotherapy responses of colorectal cancer cells in vivo. In all, our findings suggest a new mechanism involved in the regulation of the chemotherapy response of CRC and might provide new targets for CRC prevention and treatment.
引用
收藏
页码:1976 / 1985
页数:10
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