PDT-regulated immune gene prognostic model reveals tumor microenvironment in colorectal cancer liver metastases
- Jiachi Xu 1, Hui Zhou 1, Zhongtao Liu 1, Yunpeng Huang 1, Zijian Zhang 1, Heng Zou 2, Yongxiang Wang 3
- Jiachi Xu 1, Hui Zhou 1, Zhongtao Liu 1
- 1Department of General Surgery, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
- 2Department of General Surgery, The Second Xiangya Hospital of Central South University, Changsha, 410011, China. zhcsuxy@csu.edu.cn.
- 3Department of General Surgery, The Second Xiangya Hospital of Central South University, Changsha, 410011, China. 198211101@csu.edu.cn.
- 0Department of General Surgery, The Second Xiangya Hospital of Central South University, Changsha, 410011, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study identifies key genes for colorectal cancer liver metastasis (CLM) and develops a prognostic model. Photodynamic therapy (PDT) shows potential for treating CLM by targeting these genes and modulating the immune microenvironment.
Area Of Science
- Oncology
- Genomics
- Immunotherapy
Background
- Colorectal cancer liver metastasis (CLM) has a poor prognosis.
- Identifying key genes and targeted interventions for CLM is crucial.
Purpose Of The Study
- To identify key genes and construct an immune-related prognostic model for CLM.
- To analyze the colorectal cancer immune microenvironment and assess therapeutic potential.
Main Methods
- Weighted Gene Co-expression Network Analysis (WGCNA) to identify key gene modules.
- Construction of a prognostic model using immune-regulating genes.
- Analysis of methylation, mutation, Gene Ontology (GO), Gene Set Enrichment Analysis (GSEA), single-cell sequencing, and drug response data.
- Experimental validation using photodynamic therapy (PDT).
Main Results
- An immune-related prognostic model for CLM was constructed, including HSPA1A, ULBP2, RBP7, OXT, SLC11A1, INHBB, and ICOS.
- The model predicts patient prognosis and response to chemotherapy (Oxaliplatin, Cisplatin, Irinotecan, 5-Fluorouracil).
- The model correlates with an immunosuppressive microenvironment in CLM, with higher risk scores linked to weaker immune signaling.
- PDT demonstrated cytotoxic effects on colorectal cancer cells, inhibited metastasis, modulated key gene expression (SLC11A1, ICOS, HSPA1A), and suppressed immune escape.
Conclusions
- A novel immune-related prognostic model for CLM has been established.
- This model aids in predicting prognosis, chemotherapy response, and immunotherapy potential.
- PDT is a promising therapeutic strategy for CLM, targeting key genes and the tumor immune microenvironment.
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