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
相关论文
共 50 条
  • [41] ADORA1 Promotes Hepatocellular Carcinoma Progression via PI3K/AKT Pathway
    Ni, Sheng
    Wei, Qian
    Yang, Li
    ONCOTARGETS AND THERAPY, 2020, 13 : 12409 - 12419
  • [42] Upregulation of SNHG6 regulates ZEB1 expression by competitively binding miR-101-3p and interacting with UPF1 in hepatocellular carcinoma
    Chang, Lei
    Yuan, Yufeng
    Li, Cuicui
    Guo, Tao
    Qi, Haolong
    Xiao, Yusha
    Dong, Xu
    Liu, Zhisu
    Liu, Quanyan
    CANCER LETTERS, 2016, 383 (02) : 183 - 194
  • [43] Knockdown of lncRNA HOTTIP Inhibits Retinoblastoma Progression by Modulating the miR-101-3p/STC1 Axis
    Yuan, XiangWen
    Sun, Zhaoyan
    Cui, Congxian
    TECHNOLOGY IN CANCER RESEARCH & TREATMENT, 2021, 20
  • [44] CircPIAS1 promotes hepatocellular carcinoma progression by inhibiting ferroptosis via the miR-455-3p/NUPR1/FTH1 axis
    Zhang, Xiao-Yu
    Li, Shan-Shan
    Gu, Yu-Rong
    Xiao, Le-Xin
    Ma, Xin-Yi
    Chen, Xin-Ru
    Wang, Jia-Liang
    Liao, Chun-Hong
    Lin, Bing-Liang
    Huang, Yue-Hua
    Lian, Yi-Fan
    MOLECULAR CANCER, 2024, 23 (01)
  • [45] Functional analysis of miR-101-3p and Rap1b involved in hepatitis B virus-related hepatocellular carcinoma pathogenesis
    Sheng, Yanrui
    Ding, Shijia
    Chen, Ke
    Chen, Juan
    Wang, Sen
    Zou, Chengcheng
    Zhang, Jingnan
    Cao, Yiyi
    Huang, Ailong
    Tang, Hua
    BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE, 2014, 92 (02): : 152 - 162
  • [46] MiR-767-3p promotes the progression of hepatocellular carcinoma via targeting CASP-3/-9
    Wu, Maolin
    Deng, Jing
    Yao, Dejiao
    Li, Shijie
    AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2023, 15 (04): : 2926 - 2938
  • [47] miR-101-3p-mediated role of PDZK1 in hepatocellular carcinoma progression and the underlying PI3K/Akt signaling mechanism
    Huihui Gao
    Zhaofeng Gao
    Xiaobei Liu
    Xu Sun
    Zhonghui Hu
    Zhengwei Song
    Cheng Zhang
    Jianguo Fei
    Xiaoguang Wang
    Cell Division, 19
  • [48] miR-101-3p-mediated role of PDZK1 in hepatocellular carcinoma progression and the underlying PI3K/Akt signaling mechanism
    Gao, Huihui
    Gao, Zhaofeng
    Liu, Xiaobei
    Sun, Xu
    Hu, Zhonghui
    Song, Zhengwei
    Zhang, Cheng
    Fei, Jianguo
    Wang, Xiaoguang
    CELL DIVISION, 2024, 19 (01)
  • [49] CircRTN1 stimulates HMGB1 to regulate the malignant progression of papillary thyroid cancer by sponging miR-101-3p
    Zheng, Mei
    Xu, Lingli
    Wei, Cuifeng
    Guan, Wenzhen
    HORMONES-INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, 2023, 22 (02): : 281 - 293
  • [50] CircRTN1 stimulates HMGB1 to regulate the malignant progression of papillary thyroid cancer by sponging miR-101-3p
    Mei Zheng
    Lingli Xu
    Cuifeng Wei
    Wenzhen Guan
    Hormones, 2023, 22 : 281 - 293