Long non-coding RNA RP11-400N13.3 promotes the progression of colorectal cancer by regulating the miR-4722-3p/P2RY8 axis

被引:5
作者
Yang, Hongju [1 ]
Li, Qian [2 ]
Wu, Yanrui [3 ]
Dong, Jianlong [1 ]
Lao, Yaling [1 ]
Ding, Zheng [1 ]
Xiao, Changyan [1 ]
Fu, Jinxiao [4 ]
Bai, Song [1 ]
机构
[1] Kunming Med Univ, Affiliated Hosp 1, Dept Geriatr Gastroenterol, Kunming 650032, Yunnan, Peoples R China
[2] Yunnan Kunming Blood Ctr, Transfus Med Res Dept, Kunming 650106, Yunnan, Peoples R China
[3] Kunming Med Univ, Cell Biol & Genet Dept, Kunming 650500, Yunnan, Peoples R China
[4] Second Peoples Hosp Yunnan, Dept Geriatr, Kunming 650201, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
3; colorectal cancer; miR-4722-3p; P2RY8; COLON-CANCER; EXPRESSION; SIGNATURE; SURVIVAL; MARKERS; PROTEIN;
D O I
10.3892/or.2020.7755
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accumulating evidence has shown that long non-coding RNAs (lncRNAs) play significant roles in the development and progression of many types of cancer including colorectal cancer. RP11-400N13.3 is a novel lncRNA discovered recently and its biological function and underlying mechanism in colorectal cancer remain elusive. This study aimed to reveal the relationship between RP11-400N13.3 and colorectal cancer. Our results demonstrated that the expression of RP11-400N13.3 was significantly upregulated in both colorectal cancer tissues and cell lines as compared to normal adjacent tissues and normal colonic epithelial cells by RT-qPCR, respectively. Upregulation of RP11-400N13.3 was found to be correlated with a poor overall survival rate. Functional studies revealed that RP11-400N13.3 facilitated the proliferation, migration, invasion and tumor growth of colorectal cancer cells while inhibiting the apoptosis of cancer cellsin vitroandin vivo. We also observed that RP11-400N13.3 serves as a sponge for miR-4722-3p, and that P2Y receptor family member 8 (P2RY8) was predicted to be a target of miR-4722-3p by bioinformatics analysis. Western blot assay indicated that the expression of P2RY8 was negatively or positively regulated by miR-4722-3p or RP11-400N13.3. In addition, rescue experiments revealed that RP11-400N13.3 promoted proliferation, migration and invasion by directly regulating the expression of miR-4722-3p and P2RY8. In conclusion, our results revealed that RP11-400N13.3 promoted colorectal cancer progression via modulating the miR-4722-3p/P2RY8 axis, thus suggesting RP11-400N13.3 as a potential therapeutic target for the treatment of colorectal cancer.
引用
收藏
页码:2045 / 2055
页数:11
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