A computational analysis of the oncogenic and anti-tumor immunity role of P4HA3 in human cancers

PLoS Comput Biol. 2024 Nov 6;20(11):e1012284. doi: 10.1371/journal.pcbi.1012284. eCollection 2024 Nov.

Abstract

Prolyl-4-hydroxylase subunit alpha3 (P4HA3) is a triple helical procollagen synthesis protein. The role of P4HA3 in cancer development is not well known and lacks comprehensive analyses among human cancers. This study aimed to investigate the relationship between P4HA3 expression and anti-tumor immunity and its prognostic value in pan-cancer. P4HA3 expression was analyzed from TIMER2.0, GTEx, GEPIA2.0 and TCGA databases. Genetic and DNA methylation alterations, survival analysis and proteins co-expression analysis of P4HA3 in cBio Cancer Genomics Portal, TCGA, GSCA and TIMER2.0. The correlation between P4HA3 expression and immune infiltration was analyzed by TIDE, XCELL, MCPCOUNTER, and EPIC. We performed EdU and transwell experiments to evaluate the influence of P4HA3 on the proliferation, migration and invasion abilities of different tumors. Patients derived xenograft (PDX) and subcutaneous transplantation models were utilized to explore the correlation between P4HA3 and immunotherapy response in triple-negative breast cancer (TNBC). Among 33 types of cancers, P4HA3 had generally different expression between different tumors, further analysis showed that the expression of P4HA3 was correlated with the cells infiltration of the tumor microenvironment (TME). The expression of P4HA3 was positively with the cell proliferation markers and epithelial-mesenchymal transition (EMT) markers. Moreover, P4HA3 deficiency inhibited the proliferation, migration and invasion abilities of tumor cells, and promoted anti-tumor immunotherapy of PD-1/PD-L1 inhibitor. This pan-cancer analysis of P4HA3 provides a comprehensive understanding of its oncogenic and prognosis role in different cancers, P4HA3 abnormal expression could be a useful biomarker for predicting the effectiveness of immunotherapy in cancer patients.

MeSH terms

  • Animals
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism
  • Cell Line, Tumor
  • Cell Proliferation / genetics
  • Computational Biology*
  • Epithelial-Mesenchymal Transition / genetics
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunotherapy
  • Mice
  • Neoplasms* / genetics
  • Neoplasms* / immunology
  • Neoplasms* / metabolism
  • Procollagen-Proline Dioxygenase* / genetics
  • Procollagen-Proline Dioxygenase* / metabolism
  • Prognosis
  • Triple Negative Breast Neoplasms / genetics
  • Triple Negative Breast Neoplasms / immunology
  • Tumor Microenvironment / genetics
  • Tumor Microenvironment / immunology

Substances

  • Procollagen-Proline Dioxygenase
  • Biomarkers, Tumor

Grants and funding

This study was supported by the Guangzhou Basic and Applied Basic Research Project (2023A04J2445 to HYH), Science and Technology Program of Guangzhou (202201010987 to JY), President Foundation of Zhujiang Hospital, Southern Medical University (yzjj2021qn18 to JY) and Guangdong Basic and Applied Basic Research Foundation (2021A1515111138 to YSH; 2022A1515110144 to JY), National Natural Science Foundation of China (82203703 to SWR). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.