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CN 34-1304/RISSN 1674-3679

Volume 28 Issue 6
Jun.  2024
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WEI Liling, LIU Meiliang, LI Deyuan, YANG Yu, XIAO Suyang, LI Chanhua, WU Siqian, SONG Anhua, ZENG Xiaoyun. Effects of TRPV1 on biological behavior of hepatocellular carcinoma and prediction of possible mechanisms[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2024, 28(6): 691-701. doi: 10.16462/j.cnki.zhjbkz.2024.06.012
Citation: WEI Liling, LIU Meiliang, LI Deyuan, YANG Yu, XIAO Suyang, LI Chanhua, WU Siqian, SONG Anhua, ZENG Xiaoyun. Effects of TRPV1 on biological behavior of hepatocellular carcinoma and prediction of possible mechanisms[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2024, 28(6): 691-701. doi: 10.16462/j.cnki.zhjbkz.2024.06.012

Effects of TRPV1 on biological behavior of hepatocellular carcinoma and prediction of possible mechanisms

doi: 10.16462/j.cnki.zhjbkz.2024.06.012
Funds:

Guangxi Natural Science Foundation Key Program 2020GXNSFDA238002

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  • Corresponding author: ZENG Xiaoyun, E-mail: zengxiaoyun@gxmu.edu.cn
  • Received Date: 2024-02-26
  • Rev Recd Date: 2024-05-17
  • Available Online: 2024-07-13
  • Publish Date: 2024-06-10
  •   Objective  To clarify the expression of transient receptor potential vanilloid subfamily 1 (TRPV1) in hepatocellular carcinoma (HCC) and its relationship with prognosis, and to explore its effect on the biological behavior of HCC cells.  Methods  The cancer genome atlas (TCGA), genotype-tissue expression (GTEx) and gene expression ominbus (GEO) databases were utilized to verify the expression of TRPV1 in HCC and its relationship with prognosis. The effects of TRPV1 on the proliferation, migration, invasion, and cell cycle of HCC cells were detected by CCK-8 assay, scratch assay, Transwell assay, and flow cytometry. The expression of cyclin-dependent kinase 4 (CDK4) and cyclin-dependent kinase 6 (CDK6) was detected by Western blot, and the tumor proliferation ability was detected by subcutaneous tumor formation assay in nude mice. Finally, the TRPV1 co-expression network was constructed and analyzed for functional enrichment.  Results  The expression level of TRPV1 in HCC tissues was down-regulated in TCGA, GTEx, and GEO databases (P < 0.001) and was associated with a shorter overall survival time of patients (P=0.032), with an area under the ROC curve of 0.91. Overexpression of TRPV1 suppressed the proliferation, migration, and invasion ability of HCC cells, blocked cell cycle progression, and CDK4 and CDK6 protein expression levels decreased (both P < 0.05), and the opposite was true for knockdown of TRPV1 (both P < 0.05). After stable overexpression of TRPV1, the subcutaneous tumor volume of nude mice was reduced (P=0.015), the mass of nude mice was reduced (P=0.033), and the positive expression level of Ki-67 protein was down-regulated (P=0.010). TRPV1 co-expressed genes were mainly involved in the processes of RNA splicing, cell cycle protein binding, and cell proliferation.  Conclusions  TRPV1 inhibited the proliferation, migration, and invasion of HCC cells and blocked cell cycle progression, which exerted an oncogenic role in HCC and provided a new direction for the prognostic analysis and treatment of HCC.
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