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The Contribution of DNA Ligase 4 Polymorphisms to Colorectal Cancer.
Deng, Yang; Ke, Tao-Wei; Yueh, Te-Cheng; Chin, Yu-Ting; Wang, Yun-Chi; Hung, Yi-Chih; Mong, Mei-Chin; Yang, Ya-Chen; Wu, Wen-Tzu; Chang, Wen-Shin; Gu, Jian; Bau, DA-Tian; Tsai, Chia-Wen.
Affiliation
  • Deng Y; Department of General Surgery, Wuxi Branch of Shanghai Ruijin Hospital, Wuxi, P.R. China.
  • Ke TW; Department of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, P.R. China.
  • Yueh TC; Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, U.S.A.
  • Chin YT; Department of General Surgery, China Medical University Hospital, Taichung, Taiwan, R.O.C.
  • Wang YC; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
  • Hung YC; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
  • Mong MC; Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
  • Yang YC; National Defense Medical Center, Taipei, Taiwan, R.O.C.
  • Wu WT; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
  • Chang WS; Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
  • Gu J; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
  • Bau DT; Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
  • Tsai CW; Terry Fox Cancer Research Laboratory, Department of Medical Research, China Medical University Hospital, Taichung, Taiwan, R.O.C.
In Vivo ; 38(1): 127-133, 2024.
Article in En | MEDLINE | ID: mdl-38148049
ABSTRACT
BACKGROUND/

AIM:

While numerous biomarkers associated with genetic susceptibility to colorectal cancer (CRC) have been identified and validated through epidemiological studies, the specific influence of DNA ligase 4 (Lig4) genotypes remains unexplored. This study aimed to elucidate the hitherto unexamined relationship between Lig4 genotypes and CRC risk. MATERIALS AND

METHODS:

The genotypes of Lig4 rs1805388 were determined applying the polymerase chain reaction-restriction fragment length polymorphism methodology. The potential association between these genotypes and CRC risk was assessed in a Taiwanese population comprising 362 CRC cases and an equal number of age- and sex-matched controls.

RESULTS:

In the genotypic analysis, the distribution of CC, CT, and TT genotypes for Lig4 rs1805388 among CRC cases was 54.7%, 38.1%, and 7.2%, respectively. This distribution was not significantly different from the controls, which exhibited genotypic frequencies of 57.2%, 36.7%, and 6.1%, respectively (p for trend=0.7314). Analysis of allelic distribution indicated that individuals carrying the T allele of Lig4 rs1805388 displayed a slightly elevated CRC risk compared to those carrying the C allele (odds ratio=1.10, 95% confidence interval=0.87-1.39, p=0.4685).

CONCLUSION:

The variant genotypes of Lig4 rs1805388 may not serve as predictive markers for CRC risk in the Taiwanese population.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Polymorphism, Single Nucleotide Limits: Humans Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Polymorphism, Single Nucleotide Limits: Humans Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2024 Document type: Article