Carcinogenesis, Teratogenesis & Mutagenesis ›› 2025, Vol. 37 ›› Issue (3): 209-214,220.doi: 10.3969/j.issn.1004-616x.2025.03.006

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Expression and function of PABPC4 in liver cancers

LIU Xinmiao1, GAO Hongjun2, KANG Yan3, ZHANG Yun1, SUN Yulin1   

  1. 1. State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021;
    2. Department of Clinical Laboratory, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021;
    3. Department of Clinical Laboratory, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan 030013, Shanxi, China
  • Received:2025-03-27 Revised:2025-04-23 Published:2025-06-13

Abstract: OBJECTIVE: To investigate the expression characteristics, prognostic significance and functional role of cytoplasmic polyadenylate-binding protein 4 (PABPC4) in liver cancers. METHODS: RNA sequencing data of liver cancers from The Cancer Genome Atlas (TCGA) were downloaded to analyze relationships between PABPC4 expression and patient prognosis. PABPC4 knockdown and overexpression liver cancer cell lines were constructed, and expression of PABPC4, its stemness-related indexes mRNA and protein in cells were detected by real-time quantitative PCR and Western blot. Effects of PABPC4 on cell proliferation,migration,invasion and stemness were studied by CCK-8 method,plate colony formation assay, cell scratch assay and Transwell assay. RESULTS: Expression levels of PABPC4 in liver cancer tissues gradually increased with increase of pathological grade. Patients with high expression had shorter overall survival and recurrence-free survival time (P<0.05). In tumor tissues with the high expression showed upregulated PABPC4,Wnt signaling pathway-related proteins. The successfully constructed HLF cells showed stable knockdown of PABPC4 and Huh7 cells with stable overexpression. Functional experiments showed that knockdown of PABPC4 showed significantly inhibited cell proliferation, migration, invasion and colony formation (P<0.05). Overexpression of PABPC4 had the opposite effect (P<0.05). In addition, after high expression of PABPC4, the mRNA expression levels of cell stemness-related indicators (Nanog, OCT4, CD133, SOX2) were significantly increased. CONCLUSION: PABPC4 was highly expressed and was correlated with poor prognosis in liver cancer patients. PABPC4 enhanced cancer cell stemness and promoted proliferation, survival, migration, and invasion of cancer cells. Therefore, PABPC4 is a potential target for prognostic prediction and therapeutic intervention in liver cancer.

Key words: liver cancer, PABPC4, prognostic prediction, proliferation and survival, migration and invasion, cell stemness

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