Rho GTPase-activating protein 1 promotes hepatocellular carcinoma progression via modulation by CircPIP5K1A/MiR-101-3p

被引:1
|
作者
Xu, Yanni [1 ,2 ]
Liu, Xiaodi [3 ,4 ]
Cao, Jincheng [1 ,2 ]
Wu, Ye [1 ,2 ]
Jiang, Qiongchao [1 ]
Luo, Baoming [1 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Ultrasound, Guangzhou, Guangdong, Peoples R China
[2] Sun Yat sen Univ, Sun Yat sen Mem Hosp, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Guangzhou, Guangdong, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Ultrasound, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp, Lab Ultrasound Med, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
carcinogenic factor; hepatology; malignant tumor; non-coding RNAs; oncogene; CELL-PROLIFERATION; MIR-101-3P; EXPRESSION; TARGETS; PATHOGENESIS; APOPTOSIS; MIGRATION; ARHGAP1;
D O I
10.1111/hepr.13972
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AimThere has been an increased focus on regulating cell function with Rho family GTPases, including proliferation, migration/invasion, polarity, and adhesion. Due to the challenges involved in targeting Rho family GTPases directly, it may be more effective to target their regulators, such as Rho GTPase-activating protein 1 (ARHGAP1). This present research was performed to define the clinical significance of ARHGAP1 expression, as well as its regulatory mechanisms in hepatocellular carcinoma.MethodsARHGAP1 and miR-101-3p expression of liver cancer patients, and their relevance with clinicopathological characteristics and prognosis were analyzed by the Cancer Genome Atlas sequencing data, and verified using samples of hepatocellular carcinoma patients. The interactions between miR-101-3p and ARHGAP1 or circPIP5K1A were validated by bioinformatic analyses, as well as confirmed by quantitative reverse transcription polymerase chain reaction, western blotting, and dual-luciferase reporter analysis. Plate clonality assays, cell adhesion and migration experiments, and proliferation experiments were used for assessing the participation of the circPIP5K1A/miR-101-3p/ARHGAP1 pathway in cell proliferation and motility.ResultsElevated ARHGAP1 and reduced miR-101-3p expression are related to poorer survival. MiR-101-3p targets ARHGAP1 to suppress hepatocellular carcinoma cell colony formation and invasion, whereas miR-101-3p inhibitor reverses liver cancer proliferation and metastasis suppression caused by ARHGAP1 knockdown. In addition, circPIP5K1A, which is mainly distributed in the cytosol, showed carcinogenic effects by sponging miR-101-3p, thus regulating ARHGAP1 expression.ConclusionsARHGAP1 serves as an oncogenic gene in liver cancer, and the expression thereof is regulated by circPIP5K1A through sponging miR-101-3p. CircPIP5K1A regulates ARHGAP1 expression by sponging miR-101-3p. CircPIP5K1A and ARHGAP1 are carcinogenic factors in liver cancer. The circPIP5K1A/miR-101-3p/ARHGAP1 axis governs tumor progression in liver cancer.image
引用
收藏
页码:174 / 188
页数:15
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