𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Glutathione S-transferase gene polymorphisms and risk and survival of pancreatic cancer

✍ Scribed by Li Jiao; Melissa L. Bondy; Manal M. Hassan; David Z. Chang; James L. Abbruzzese; Douglas B. Evans; Michael H. Smolensky; Donghui Li


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
165 KB
Volume
109
Category
Article
ISSN
0008-543X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

BACKGROUND.

Pancreatic cancer is a multifactorial disease with metastasis‐prone and therapy‐resistant nature. The authors hypothesized that genetic variants of glutathione S‐transferase (GST) affect detoxification of carcinogens and anticancer agents in the human pancreas and, thus, the risk and survival of pancreatic cancer.

METHODS.

Genotypes of GSTM1, GSTT1, and GSTP1 were determined in 352 patients with pancreatic ductal adenocarcinoma and in a control group of 315 healthy, non‐Hispanic whites (frequency‐matched by age and sex). Survival analysis was performed in a subset of 290 patients. Epidemiological and clinical information was obtained. A multiple unconditional logistic regression model, a Cox proportional hazards model, and log‐rank tests were used for statistical analysis.

RESULTS.

No significant main effects of any of 3 GST genes on the risk of pancreatic cancer were observed. Subgroup analysis showed that older individuals (aged ≥62 years) who carried the GSTP1*C (^105^Val‐^114^Val) containing genotype tended to have a reduced risk compared with younger individuals who carried the non‐*C genotype (for sex and pack‐years of smoking, the adjusted odd ratio was 0.54; 95% confidence interval [95% CI], 0.29–1.02). In a survival analysis of 138 patients who received 5‐flurorouracil, patients who carried the GSTP1*C containing genotype had a significantly longer survival than patients who carried the non‐*C genotype (multivariate hazard ratio, 0.45; 95% CI, 0.22–0.94).

CONCLUSIONS.

The GSTP1*C variant conferred a possible protective effect against pancreatic cancer in older individuals and a significant survival advantage in patients who received 5‐florouracil. The current findings must be confirmed before further inferences can be made. Cancer 2007 © 2007 American Cancer Society.


📜 SIMILAR VOLUMES


Glutathione S-transferase polymorphisms
✍ Stacy A. Geisler; Andrew F. Olshan; Jianwen Cai; Mark Weissler; Joanna Smith; Do 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 445 KB 👁 2 views

Background. The purpose of this study was to evaluate the prognostic ability of polymorphisms of three genes involved in the metabolism of tobacco carcinogens (GSTT1, GSTM1, GSTP1) and one polymorphism of a DNA repair gene (XRCC1) for patients diagnosed with squamous cell carcinoma (SCC). Methods.

Polymorphisms of the glutathione S-trans
✍ Michael B. Oude Ophuis; Hennie M. J. Roelofs; Piet A. van den Brandt; Wilbert H. 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 86 KB 👁 2 views

## Abstract ## Background. Factors determining the individual susceptibility to head and neck squamous cell carcinoma (HNSCC) are still largely unknown. An imbalance between enzymes involved in the toxification and detoxification of (pre)‐carcinogens closely related to HNSCC, which may appear duri

Association between a glutathione S-tran
✍ Carol Sweeney; Christine B. Ambrosone; Lija Joseph; Angie Stone; Laura F. Hutchi 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 French ⚖ 82 KB

## Abstract Glutathione __S__‐transferase (GST) enzymes detoxify chemotherapeutic drugs, and several studies have reported differences in survival for cancer patients who have variant genotypes for GSTP1, GSTM1 or GSTT1 enzymes. A recently described polymorphism alters hepatic expression of GSTA1,

Glutathione-S-transferase polymorphisms
✍ Lie Cheng; Erich M. Sturgis; Susan A. Eicher; David Char; Margaret R. Spitz; Qin 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 French ⚖ 106 KB 👁 2 views

Differences in genetic susceptibility to tobacco-induced carcinogenesis appear to modulate an individual's risk of squamous-cell carcinoma of the head and neck (SCCHN). Risk for SCCHN may be associated with the null alleles of the carcinogen-metabolizing genes glutathione-S-transferase (GST) T1 and