Related Experiment Video
Updated: Jun 18, 2025

Analysis of Human T Cell Activity in an Allogeneic Co-Culture Setting of Pre-Treated Tumor Cells
Published on: March 7, 2025
Pan-cancer analysis of T-cell proliferation regulatory genes as potential immunotherapeutic targets
Ruqiong Wei1, Shihui Xiao2, Shijian Zhao3
1Department of Rehabilitation Medicine, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi 530021, China.
Abstract:
T cells are the key to killing tumor cells. However, the exact mechanism of their role in cancer is not fully understood. Therefore, a comprehensive understanding of the role of T-cell proliferation regulatory genes in tumors is needed. In our study, we investigated the expression levels of genes controlling T-cell proliferation, their impact on prognosis, and their genetic variations. Additionally, we explored their associations with TMB, MSI, ESTIMATEScore, ImmuneScore, StromalScore, and immune cell infiltration. We examined the role of these genes in cancer-related pathways using GSEA. Furthermore, we calculated their activity levels across various types of cancer. Drug analysis was also conducted targeting these genes. Single-cell analysis, LASSO Cox model construction, and prognosis analysis were performed. We observed distinct expression patterns of T-cell proliferation regulatory genes across different malignant tumors. Their abnormal expression may be caused by CNA and DNA methylation. In certain cancers, they also showed complex associations with TMB and MSI. Moreover, in many tumors, they exhibited significant positive correlations with ESTIMATEScores, ImmuneScore, and StromalScore. Additionally, in most tumors, their GSVA scores were significantly positively correlated with various T-cell subtypes. GSEA analysis revealed their involvement in multiple immune pathways. Furthermore, we found that model scores were associated with patient prognosis and related to tumor malignancy progression. T-cell proliferation regulatory genes are closely associated with the tumor immune microenvironment (TIM), especially T cells. Targeting them may be an essential approach for cancer immunotherapy.
Insights
Understanding T-cell proliferation regulatory genes is crucial for cancer immunotherapy. These genes significantly impact the tumor immune microenvironment and patient prognosis, offering potential therapeutic targets.
Area of Science:
- Immunology
- Oncology
- Genetics
Background:
- T cells are vital for anti-tumor immunity, but their precise role in cancer progression remains unclear.
- A deeper understanding of T-cell proliferation regulatory genes is needed to elucidate their function in tumorigenesis.
- Investigating these genes can reveal novel therapeutic strategies for cancer immunotherapy.
Purpose of the Study:
- To analyze the expression, prognostic impact, and genetic variations of T-cell proliferation regulatory genes in various cancers.
- To explore the associations of these genes with tumor mutational burden (TMB), microsatellite instability (MSI), and immune microenvironment scores.
- To evaluate the role of these genes in cancer-related pathways and their potential as therapeutic targets.
Main Methods:
- Gene expression analysis, genetic variation assessment, Gene Set Enrichment Analysis (GSEA).
- Tumor Mutational Burden (TMB), Microsatellite Instability (MSI), ESTIMATE, ImmuneScore, StromalScore analyses.
- LASSO Cox regression, single-cell analysis, and drug sensitivity analysis.
Main Results:
- Distinct expression patterns of T-cell proliferation genes were observed across different cancers, influenced by copy number alterations (CNA) and DNA methylation.
- These genes showed complex associations with TMB and MSI, and significant positive correlations with ESTIMATE, Immune, and Stromal scores.
- Enrichment analysis confirmed their involvement in immune pathways, with their activity correlating with T-cell infiltration and patient prognosis.
Conclusions:
- T-cell proliferation regulatory genes are integral to the tumor immune microenvironment (TIM), particularly T-cell populations.
- Their expression patterns and prognostic significance highlight their potential as biomarkers and therapeutic targets in cancer immunotherapy.
- Targeting these genes may represent a promising strategy to enhance anti-tumor immunity and improve patient outcomes.
More Related Videos
07:55Flow Cytometry-Based Isolation and Therapeutic Evaluation of Tumor-Infiltrating Lymphocytes in a Mouse Model of Pancreatic Cancer
Published on: January 17, 2025
09:32Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
Related Concept Videos
Tumor Immunotherapy
Cancer-Critical Genes II: Tumor Suppressor Genes
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
Abnormal Proliferation
Targeted Cancer Therapies
There are several types of targeted therapies against...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...