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Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
Association between TIM-3 polymorphisms and cancer risk: a meta-analysis
Hongyan Fang1,2, Cheng Yuan3, Xinsheng Gu4
1Department of Oncology, The Fifth Hospital of Wuhan, Wuhan 430050, China.
Single nucleotide polymorphisms (SNPs) in T-cell immunoglobulin- and mucin-domain-containing molecule 3 (TIM-3) are linked to increased cancer risk. This meta-analysis confirms TIM-3 polymorphisms are associated with higher susceptibility to various human cancers.
Area of Science:
- Genetics
- Oncology
- Immunology
Background:
- Single nucleotide polymorphisms (SNPs) in T-cell immunoglobulin- and mucin-domain-containing molecule 3 (TIM-3) have been individually linked to cancer risk.
- Further investigation is needed to confirm the correlation between TIM-3 polymorphisms and human cancer susceptibility.
Purpose of the Study:
- To evaluate the association between TIM-3 polymorphisms and the risk of developing human cancers.
- To synthesize existing evidence through a comprehensive meta-analysis.
Main Methods:
- A systematic literature search was conducted across electronic databases.
- Two independent reviewers selected studies, extracted data, and assessed study quality.
- Meta-analysis was performed using STATA 13.0, calculating crude odds ratios (OR) and 95% confidence intervals (CI).
Main Results:
- The meta-analysis included 4,852 participants (2,229 cases, 2,623 controls).
- TIM-3 SNPs (-1516G/T, -574G/T, +4259T/G) and haplotypes were significantly associated with increased overall cancer risk.
- Subgroup analyses revealed specific associations for individual SNPs with digestive system cancers and hospital-based populations. The GGG haplotype showed a 2.614-fold increased odds of cancer.
Conclusions:
- TIM-3 SNPs (-1516G/T, -574G/T, +4259T/G) and observed haplotypes are associated with an elevated risk of developing human cancers.
- These findings highlight the role of TIM-3 genetic variations in cancer susceptibility.
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