Integrative analysis of the PSMA family identifies PSMA6 as an adverse prognostic biomarker promoting bladder cancer cell proliferation

TL;DR

This study finds that PSMA6 is a biomarker linked to worse outcomes in bladder cancer and may help predict immunotherapy response.

Contribution

The study identifies PSMA6 as a novel adverse prognostic biomarker and potential immunotherapy predictor in bladder cancer.

Findings

PSMA6 is upregulated in bladder cancer and linked to poor prognosis and tumor malignancy.

PSMA6 is associated with immune-related activities and tumor-infiltrating immune cells in the tumor microenvironment.

Knockdown of PSMA6 suppresses bladder cancer cell proliferation in vitro and in vivo.

Abstract

Proteasome subunit alpha members (PSMAs) are reported to be involved in diverse biological processes, and mounting evidence indicates that PSMAs have been implicated in the carcinogenesis of various malignancies. Nevertheless, there is a scarcity of reports on the expression, prognostic significance, and potential functions of the PSMA family in bladder cancer (BLCA).

We utilized the TCGA, GEO, TIMER, UALCAN, and HPA databases to evaluate the expression of PSMAs in BLCA. Survival analyses were performed using Kaplan-Meier methods. The validation of PSMA6 dysregulation in human BLCA samples encompassed western blotting and immunohistochemistry. For the enrichment of biological processes, we applied Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and Gene Set Enrichment Analyses (GSEA). Subsequent analyses involved the exploration of correlations between gene expression and Immune-related effects. In-depth investigations into the role of PSMA6 in BLCA were conducted through both in vitro and in vivo experiments.

We demonstrated that PSMA6 was upregulated among PSMAs in BLCA, and overexpression of PSMA6 was associated with unfavorable prognosis and tumor malignancy. Enrichment analyses disclosed the involvement of PSMA6 in immune-related activities within the tumor microenvironment. Furthermore, the expression of PSMA6 was closely correlated with tumor-infiltrating immune cells (TICs) and immune checkpoints (ICPs). Besides, we also revealed that BLCA patients with high PSMA6 expression would have better immunotherapy response. Functional studies demonstrated that PSMA6 knockdown suppressed BLCA cell proliferation in vitro and in vivo.

Our findings suggested that PSMA6 might function as an unfavorable prognostic biomarker, fostering BLCA cell proliferation, while also potentially serving as a predictive indicator for the efficacy of immunotherapy in BLCA patients

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