Interaction Analysis of SHMT1/2 Gene Variants with HCC in Chinese Patients DOI Creative Commons
Yaohui Sun, Jie Gao, Chengcheng Shi

et al.

Research Square (Research Square), Journal Year: 2022, Volume and Issue: unknown

Published: Dec. 5, 2022

Abstract Background: Metabolic reprogramming caused by SHMT1/2, as key enzymes in one-carbon metabolism, has been considered to play a critical role occurrence and progression of hepatocellular carcinoma (HCC). However, the associations between single nucleotide polymorphisms (SNPs) SHMT1/2 genes susceptibility HCC remains unknown. The purpose this study was investigate relation four candidate SNPs risk Chinese population. Materials methods: A case-control including 514 patients 234 controls performed determine risk,isolated via mass spectrometry. Results: Our data revealed that SHMT2 rs2229717 significantly associated with when compared healthy under multiple genetic models (Allele T: odds ratio (OR) = 0.73, P=0.023; Dominant Model: OR 0.72, P=0.044). When our cohort stratified sex, male subjects T allele TT genotype for exhibited decreased (OR=0.67, 95%CI=0.50-0.91; OR=0.43, 95%CI=0.18-0.99). In addition, after age stratification executed, results showed both GT were less common 50 years old. Conclusion: These indicate rs2229717is predisposing factor may affect various or sex subgroups, suggesting rs2229717may be useful predictive diagnostic tool some populations.

Language: Английский

Transcription factor 3 enhances hepatocellular carcinoma metastasis by upregulating MMP11 DOI Creative Commons

Hongpeng Tian,

Cheng Huang,

Huafang Hou

et al.

Research Square (Research Square), Journal Year: 2023, Volume and Issue: unknown

Published: Dec. 16, 2023

Abstract Transcription factor 3 (TCF3) has a vital role in tumor occurrence and progression. However, the specific functions underlying mechanisms of dysregulated TCF3 hepatocellular carcinoma (HCC) is not thoroughly characterized. Thus, we explored levels roles HCC samples. In addition, knockdown overexpression models were developed via lentiviral vectors cells. Transwell as well vivo metastasis experiments performed to measure effects on cell metastasis. Then, reverse transcription-quantitative PCR, serial deletion, western blotting, site-directed mutagenesis, chromatin immunoprecipitation dual-luciferase reporter assays done determine involved pathomechanisms. markedly elevated samples, correlated with poor prognosis. Besides, overexpressed promoted invasion migration, while repressed growth. mediated MMP11 expressions. TCF3-associated migration its attenuated knockdown-mediated repression human-derived positively expression level. Overall, these findings highlighted that could be regarded prognostic biomarker regulator.

Language: Английский

Citations

0

Interaction Analysis of SHMT1/2 Gene Variants with HCC in Chinese Patients DOI Creative Commons
Yaohui Sun, Jie Gao, Chengcheng Shi

et al.

Research Square (Research Square), Journal Year: 2022, Volume and Issue: unknown

Published: Dec. 5, 2022

Abstract Background: Metabolic reprogramming caused by SHMT1/2, as key enzymes in one-carbon metabolism, has been considered to play a critical role occurrence and progression of hepatocellular carcinoma (HCC). However, the associations between single nucleotide polymorphisms (SNPs) SHMT1/2 genes susceptibility HCC remains unknown. The purpose this study was investigate relation four candidate SNPs risk Chinese population. Materials methods: A case-control including 514 patients 234 controls performed determine risk,isolated via mass spectrometry. Results: Our data revealed that SHMT2 rs2229717 significantly associated with when compared healthy under multiple genetic models (Allele T: odds ratio (OR) = 0.73, P=0.023; Dominant Model: OR 0.72, P=0.044). When our cohort stratified sex, male subjects T allele TT genotype for exhibited decreased (OR=0.67, 95%CI=0.50-0.91; OR=0.43, 95%CI=0.18-0.99). In addition, after age stratification executed, results showed both GT were less common 50 years old. Conclusion: These indicate rs2229717is predisposing factor may affect various or sex subgroups, suggesting rs2229717may be useful predictive diagnostic tool some populations.

Language: Английский

Citations

0