Identification of a Novel Mesenchymal Stem Cell-Related Signature for Predicting the Prognosis and Therapeutic Responses of Bladder Cancer
- Enguang Yang 1, Luhua Ji 1, Xinyu Zhang 1, Suoshi Jing 1, Pan Li 1, Hanzhang Wang 2, Luyang Zhang 1, Yuanfeng Zhang 1, Li Yang 1, Junqiang Tian 1, Zhiping Wang 1
- Enguang Yang 1, Luhua Ji 1, Xinyu Zhang 1
- 1Institute of Urology, Key Laboratory of Gansu Province for Urological Diseases, Gansu Urological Clinical Center, Lanzhou University Second Hospital, Lanzhou 730030, China.
- 2Department of Pathology and Laboratory Medicine, Legorreta Cancer Center at Brown University, The Warren Alpert Medical School of Brown University, Brown University Health, Providence 02912, Rhode Island, USA.
- 0Institute of Urology, Key Laboratory of Gansu Province for Urological Diseases, Gansu Urological Clinical Center, Lanzhou University Second Hospital, Lanzhou 730030, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study developed a five-gene prognostic model for bladder cancer (BC) using mesenchymal stem cell (MSC) markers to predict patient outcomes and treatment response. The model identifies high-risk patients who may benefit from specific chemotherapy drugs.
Area Of Science
- Oncology
- Cancer Biology
- Stem Cell Research
Background
- Mesenchymal stem cells (MSCs) exhibit unique migratory patterns toward tumors, influencing cancer progression, treatment resistance, and immunosuppression.
- Understanding the role of MSCs in bladder cancer (BC) is crucial for developing effective prognostic and therapeutic strategies.
Purpose Of The Study
- To formulate a prognostic model based on MSC-associated markers for predicting clinical outcomes in bladder cancer patients.
- To assess the model's ability to predict responses to chemotherapy and immunotherapy in bladder cancer.
Main Methods
- Utilized clinical and transcriptome data from TCGA-BLCA and GSE31684 databases.
- Applied weighted gene coexpression network analysis to identify MSC-correlated genes.
- Developed a risk signature using univariate and LASSO Cox regression, validated by molecular docking for drug targeting.
Main Results
- A five-gene prognostic model (ZNF165, MXRA7, CEMIP, ARL4C, CERCAM) was established for MSCs in bladder cancer.
- High-MSC-risk patients showed unfavorable prognoses, while low-MSC-risk patients responded better to immunotherapy.
- Specific chemotherapy drug sensitivities varied between high-risk (gemcitabine, vincristine, paclitaxel, gefitinib, sorafenib) and low-risk (cisplatin) groups.
Conclusions
- The five-gene MSC prognostic model effectively predicts bladder cancer outcomes and treatment response.
- Identified genes (ZNF165, MXRA7, CEMIP, ARL4C, CERCAM) are potential targets for anti-MSC therapies.
- This model offers insights for personalized treatment strategies in bladder cancer management.
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