SPRY4-IT1 promotes survival of colorectal cancer cells through regulating PDK1-mediated glycolysis

被引:10
|
作者
Liu, Shengyuan [1 ]
Huang, Feng [1 ]
Ye, Qing [1 ]
Li, Yangming [1 ]
Chen, Jinhu [1 ]
Huang, Hong [1 ]
机构
[1] Fujian Med Univ Canc Hosp, Fujian Canc Hosp, Dept Gastroenterol, 420 Fuma Rd, Fuzhou 350014, Fujian, Peoples R China
关键词
SPRY4-IT1; colorectal cancer (CRC); proliferation; glycolysis; molecular target; NONCODING RNA SPRY4-IT1; PREDICTS POOR-PROGNOSIS; LNCRNA SPRY4-IT1; UP-REGULATION; INVASION; PROLIFERATION; MIGRATION;
D O I
10.1080/19768354.2020.1784274
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Colorectal cancer (CRC) becomes the third leading cause of cancer-related deaths worldwide recently. The prognosis of CRC is still poor in decades, and targeted therapy is still a potential effective treatment. Long non-coding RNAs (lncRNAs) could regulate series of cellular functions and developmental processes. LncRNA-SPRY4-IT1 (GenBank ID AK024556) is derived from an intron of the SPRY4 gene, which was highly expressed in melanoma cells and affected the progression of multiple types of cancers. However, the mechanism of SPRY4-IT1 in CRC progression remains unclear. Herein, we found the high level of SPRY4-IT1 in human colorectal cancer (CRC) tissues and cells, and correlated with patients' prognosis. We further noticed that SPRY4-IT1 regulated CRC cell growth and glycolysis, and promoting PDK1 expression. Our data further confirmed that SPRY4-IT1 regulated CRC progression targeting PDK1. We therefore thought SPRY4-IT1 could serve as a promising molecular target for the treatment of CRC.
引用
收藏
页码:220 / 227
页数:8
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