SMC2 as a potential prognostic biomarker in lung adenocarcinoma and its correlation with immune microenvironment
- Fuqiang Zheng 1, Yu Li 1, Huiguo Chen 2, You Peng 3, Xiaocai Tian 1
- Fuqiang Zheng 1, Yu Li 1, Huiguo Chen 2
- 1Department of Oncology, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University, Changsha, Hunan 410000, P.R. China.
- 2Department of Thoracic surgery, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University, Changsha, Hunan 410000, P.R. China.
- 3Department of Geriatric, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University, Changsha, Hunan 410000, P.R. China.
- 0Department of Oncology, Hunan Provincial People's Hospital/First Affiliated Hospital of Hunan Normal University, Changsha, Hunan 410000, P.R. China.
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View abstract on PubMed
Summary
This summary is machine-generated.Structural maintenance of chromosome 2 (SMC2) is highly expressed in lung adenocarcinoma (LUAD), correlating with poor prognosis and immune suppression. Targeting SMC2 may improve LUAD treatment outcomes.
Area Of Science
- Oncology
- Molecular Biology
Background
- Structural maintenance of chromosome 2 (SMC2) is implicated in various cancers.
- Its specific role in lung adenocarcinoma (LUAD) requires further elucidation.
Purpose Of The Study
- To investigate the expression, prognostic significance, and immune-related functions of SMC2 in LUAD.
- To explore SMC2 as a potential therapeutic target for LUAD.
Main Methods
- Bioinformatic analysis using TCGA, TIMER 2.0, TISIDB, cBioportal, GO, GSEA, KEGG.
- Quantitative PCR and immunohistochemistry on LUAD tissues.
- Clinical data analysis of 70 LUAD patients.
Main Results
- SMC2 was significantly upregulated in LUAD tissues and cell lines, linked to adverse clinicopathological features and poor prognosis.
- SMC2 expression correlated with cell cycle regulation and suppressive immune cells (e.g., B cells) in LUAD.
- High SMC2 expression was associated with immunosuppressive genes, poor response to immunotherapy, and potentially promotes LUAD progression.
Conclusions
- SMC2 is a potential biomarker for poor prognosis in LUAD.
- SMC2 may play a role in immune evasion and malignant progression of LUAD.
- Targeting SMC2 could offer a novel therapeutic strategy for improving LUAD patient outcomes.
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