The role of PSMC4 in non-small cell lung cancer: implications for prognosis, diagnosis, and immune microenvironment modulation
- Lili Zhu 1, Yuanjun Li 2, Yunfei Xu 2,3, Jian Lei 1
- Lili Zhu 1, Yuanjun Li 2, Yunfei Xu 2,3
- 1Department of Pathology, Hunan Cancer Hospital, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, China.
- 2Department of Physiology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.
- 3Postdoctoral Research Station of Biology, School of Basic Medical Science, Central South University, Changsha, Hunan, China.
- 0Department of Pathology, Hunan Cancer Hospital, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha, Hunan, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Proteasome 26S subunit ATPase 4 (PSMC4) is elevated in non-small cell lung cancer (NSCLC), correlating with advanced stages and poor survival. PSMC4 shows promise as a diagnostic and prognostic biomarker for NSCLC.
Area Of Science
- Oncology
- Molecular Biology
- Biochemistry
Background
- Non-small cell lung cancer (NSCLC) is a leading cause of cancer mortality, necessitating novel biomarkers for improved diagnosis and treatment.
- Proteasome 26S subunit ATPase 4 (PSMC4), a key component of the proteasome, is implicated in protein degradation and tumor progression, but its specific role in NSCLC is not fully understood.
Purpose Of The Study
- To investigate the expression profile of PSMC4 in NSCLC.
- To evaluate the correlation of PSMC4 with clinicopathological features, diagnostic value, and prognostic significance.
- To explore the role of PSMC4 in the tumor microenvironment and its potential as a therapeutic target.
Main Methods
- Bioinformatic analysis of PSMC4 expression in NSCLC datasets.
- Correlation analysis with clinicopathological characteristics, survival data, and tumor microenvironment factors.
- Receiver operating characteristic (ROC) curve analysis for diagnostic efficacy.
- Univariate and multivariate Cox regression for prognostic assessment.
- Immunohistochemistry and functional assays (cell proliferation, xenograft models) to validate findings.
Main Results
- PSMC4 expression is significantly elevated in NSCLC, particularly lung adenocarcinoma, and correlates with advanced T, N, and pathological stages.
- PSMC4 demonstrates high diagnostic sensitivity and specificity.
- Elevated PSMC4 levels are associated with reduced overall survival, disease-specific survival, and progression-free intervals, identifying it as an independent prognostic marker.
- PSMC4 is linked to key biological processes like DNA replication and cell cycle pathways (G2/M DNA damage checkpoint) and signaling pathways (WNT).
- Immunohistochemistry confirms increased PSMC4 expression in NSCLC tissues, and functional studies show PSMC4 promotes cancer cell proliferation and tumor growth.
Conclusions
- PSMC4 serves as a valuable diagnostic and prognostic biomarker for NSCLC.
- PSMC4 plays a significant role in NSCLC progression and the tumor immune microenvironment.
- Targeting PSMC4 presents a potential therapeutic strategy for NSCLC treatment.
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