Liu Shengyuan, Huang Feng, Ye Qing, Li Yangming, Chen Jinhu, Huang Hong
Department of Gastroenterology, Fujian Cancer Hospital, Fujian Medical University Cancer Hospital, Fuzhou, People's Republic of China.
Anim Cells Syst (Seoul). 2020 Jun 25;24(4):220-227. doi: 10.1080/19768354.2020.1784274.
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.
近年来,结直肠癌(CRC)成为全球癌症相关死亡的第三大主要原因。几十年来,CRC的预后仍然很差,靶向治疗仍然是一种潜在的有效治疗方法。长链非编码RNA(lncRNAs)可以调节一系列细胞功能和发育过程。LncRNA-SPRY4-IT1(GenBank ID AK024556)来源于SPRY4基因的一个内含子,在黑色素瘤细胞中高度表达,并影响多种类型癌症的进展。然而,SPRY4-IT1在CRC进展中的机制仍不清楚。在此,我们发现人结直肠癌(CRC)组织和细胞中SPRY4-IT1水平较高,并与患者预后相关。我们进一步注意到,SPRY4-IT1调节CRC细胞生长和糖酵解,并促进PDK1表达。我们的数据进一步证实,SPRY4-IT1通过靶向PDK1调节CRC进展。因此,我们认为SPRY4-IT1可以作为治疗CRC的一个有前景的分子靶点。