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DOI 10.1002/jso.21643

Медицинская библиотека · Journal of surgical oncology · 2010

Influence of glutathione-S-transferase theta (GSTT1) and micro (GSTM1) gene polymorphisms on the susceptibility of hepatocellular carcinoma in Taiwan.

Kao Chia-Chun, Chen Mu-Kuan, Kuo Wu-Hsien, Chen Tzy-Yen, Su Shih-Chi, Hsieh Yi-Hsien, Liu Chuen-Lan, Chou Ming-Chih, Tsai Hsiu-Ting, Yang Shun-Fa

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND AND

OBJECTIVES

Hepatocellular carcinoma (HCC) is one of the most frequent malignant neoplasms worldwide and is the second leading cause of cancer death in Taiwan. Genetic polymorphism has been reported as a factor for increased susceptibility of HCC. Glutathione-S-transferases theta (GSTT1) and micro (GSTM1) play essential roles in detoxification of ingested xenobiotics and modulation of the susceptibility of gene-related cancer. The aim of this study was to estimate the relationships between these two gene polymorphisms and HCC risk and clinicopathological status in Taiwanese.

METHODS

Polymerase chain reaction (PCR) was used to determine gene polymorphisms of 102 patients with HCC and 386 healthy controls.

RESULTS

Both gene polymorphisms were not associated with the clinical pathological status of HCC and serum levels of liver-related clinical pathological markers. While no relationship between GSTM1 gene polymorphism and HCC susceptibility was found, individuals of age <56 years old with GSTT1 present genotype have a risk of 2.77-fold (95% CI: 1.09-7.09) for HCC compared to that with null variant, after adjustment for other confounders.

CONCLUSIONS

GSTT1 and GSTM1 null genotypes do not associate with increased risk of HCC.

Для цитирования: Kao Chia-Chun, Chen Mu-Kuan, Kuo Wu-Hsien, Chen Tzy-Yen, Su Shih-Chi, Hsieh Yi-Hsien, Liu Chuen-Lan, Chou Ming-Chih, Tsai Hsiu-Ting, Yang Shun-Fa. Influence of glutathione-S-transferase theta (GSTT1) and micro (GSTM1) gene polymorphisms on the susceptibility of hepatocellular carcinoma in Taiwan.. Journal of surgical oncology. 2010. DOI: 10.1002/jso.21643.

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