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Published on: October 27, 2020
Genetic variation in the TGF-β signaling pathway and colon and rectal cancer risk
Martha L Slattery1, Jennifer S Herrick, Abbie Lundgreen
1Department of Internal Medicine, University of Utah Health Sciences Center, 295 Chipeta Way, Salt Lake City, Utah 84108, USA. marty.slattery@hsc.utah.edu
Background:
The TGF-β signaling pathway is an essential regulator of many cellular process involved in carcinogenesis. Smad proteins are central to the function of TGF-β signaling. In this study, we evaluated genetic variation in TGFβ1, TGFβR1, Smad1, Smad2, Smad3, and Smad4 and risk of colon and rectal cancer.
Methods:
Data are from a large case-control study of colon (n = 1,444 cases, 1,841 controls) and rectal (n = 754 cases, 856 controls) cancer participants with DNA.
Results:
Both TGFβ1 rs1800469 and rs4803455 were associated with colon cancer [odds ratio (OR) = 0.65 and 1.43, 95% CI = 0.51-0.84 and 1.18-1.73, respectively) but not rectal cancer. Likewise, 1 of 3 tagSNPs for TGFβR1, 2 of the 4 tagSNPs for Smad2, and 4 of 37 Smad3 tagSNPs were associated with colon cancer. Fewer significant associations were observed for rectal cancer, with only 1 tagSNP in Smad2 and 3 tagSNP in Smad3 having 95% CIs excluding 1.0. Several Smad3 tagSNPs were only associated with CpG island methylator phenotype. We observed several statistically significant interactions between genetic variation in the TGF-β signaling pathway and NFκB1, further illustrating its involvement in proposed mechanisms. In addition, we observed statistically significant interaction between TGFβ1, TGFβR1, and Smad3 and cigarette smoking, aspirin use, and estrogen status for both colon and rectal cancers. Variation in TGFβ1, TGFβR1, and Smad3 seemed to influence survival after diagnosis of colon and rectal cancer.
Conclusions:
These findings provide further support for genetic variation in the TGF-β signaling pathway and risk of developing both colon and rectal cancers.
Impact:
Insight into biological pathways is provided.
Insights
Genetic variations in the TGF-β signaling pathway, including TGFβ1 and Smad genes, are linked to colon and rectal cancer risk. These findings highlight the pathway's role in cancer development and survival.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- The transforming growth factor-beta (TGF-β) signaling pathway is crucial in cellular processes and carcinogenesis.
- Smad proteins are key mediators of TGF-β signaling.
- Genetic variations in this pathway may influence cancer risk.
Purpose of the Study:
- To investigate the association between genetic variations in TGFβ1, TGFβR1, Smad1, Smad2, Smad3, and Smad4 and the risk of colon and rectal cancer.
- To explore interactions between these genetic variations and environmental factors.
- To assess the impact of these variations on cancer survival.
Main Methods:
- A large case-control study was conducted.
- Participants included 1,444 cases and 1,841 controls for colon cancer, and 754 cases and 856 controls for rectal cancer.
- DNA was analyzed for genetic variations.
Main Results:
- Specific variations in TGFβ1 (rs1800469, rs4803455) were associated with colon cancer risk.
- Several tagSNPs in TGFβR1, Smad2, and Smad3 were linked to colon cancer.
- Fewer significant associations were found for rectal cancer, but interactions with smoking, aspirin, and estrogen were observed for both.
- Genetic variations in TGFβ1, TGFβR1, and Smad3 appeared to affect survival.
Conclusions:
- Genetic variations in the TGF-β signaling pathway are associated with the risk of colon and rectal cancers.
- The pathway's genetic variations interact with environmental factors, influencing cancer development and outcomes.
- This study provides insights into the biological pathways involved in colorectal carcinogenesis.
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