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Common immunological and prognostic features of lung and bladder cancer via smoking-related genes: PRR11 gene as
YaXuan Wang1, HaiXia Zhu2, Lu Zhang1
1Department of Urology, The First Affiliated Hospital of Harbin Medical University, Harbin, China.
Journal of Cellular and Molecular Medicine
|May 18, 2024
Summary
This study identifies PRR11 as a key smoking-related gene impacting prognosis and immunotherapy response in non-small-cell lung cancer (NSCLC) and bladder cancer (BLCA). PRR11 influences PDL1 expression via SPDL1, affecting treatment efficacy.
Area of Science:
- Oncology
- Molecular Biology
- Immunotherapy
Background:
- Smoking is a significant risk factor for non-small-cell lung cancer (NSCLC) and bladder urothelial carcinoma (BLCA).
- A prognostic marker linking smoking-related genes to prognosis and immune checkpoint therapy efficacy is lacking for these cancers.
Purpose of the Study:
- To identify smoking-related genes in NSCLC and BLCA that predict prognosis and correlate with immune checkpoint therapy.
- To investigate the role of PRR11 as a prognostic marker and its impact on immunotherapy.
- To explore the regulatory network involving PRR11, SPDL1, and hsa-miR-200b-3p.
Main Methods:
- Differential gene expression analysis in NSCLC and BLCA.
- Prognostic model construction based on PRR11 co-expressed genes.
- Molecular docking and tissue microarray analyses to study PRR11-SPDL1 interaction.
- miRNA analysis.
Main Results:
- PRR11 identified as a crucial smoking-associated gene influencing cancer stemness and immunotherapy efficacy.
- A prognostic model based on PRR11 co-expressed genes demonstrated prognostic value in BLCA and NSCLC.
- PRR11 regulates PDL1 expression through SPDL1, impacting immunotherapeutic outcomes.
- hsa-miR-200b-3p was implicated in the PRR11-SPDL1 regulatory axis.
Conclusions:
- PRR11 is a key regulator of prognosis and immunotherapy response in smoking-related NSCLC and BLCA.
- The PRR11-SPDL1-PDL1 pathway is a critical determinant of immunotherapeutic efficacy.
- PRR11 and its associated regulatory network offer potential therapeutic targets for NSCLC and BLCA.
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