@article {CSEJTEI1917, author = {ANDRAS CSEJTEI and ANTAL TIBOLD and ZSUZSA VARGA and KATALIN KOLTAI and AGOSTON EMBER and ZSUZSA ORSOS and GERGELY FEHER and ORS PETER HORVATH and ISTVAN EMBER and ISTVAN KISS}, title = {GSTM, GSTT and p53 Polymorphisms as Modifiers of Clinical Outcome in Colorectal Cancer}, volume = {28}, number = {3B}, pages = {1917--1922}, year = {2008}, publisher = {International Institute of Anticancer Research}, abstract = {Background: Cancer of the colorectal region is the second most frequent cause of death among malignant diseases. The influence of two allelic polymorphisms of GSTM1 and GSTT1, and that of p53 gene codon 72 on colon cancer was investigated. Patients and Methods: Intraoperatively removed tissue samples were processed from colorectal cancer patients. Cancer-free human samples were used as matched controls. Samples were digested with proteinase-K. DNA solution was used for PCR amplification. Results: No significant difference was found between tumor patients and controls in the investigated polymorphisms. A significant association was found in Dukes{\textquoteright} B stage patients between the GSTM1 and p53 gene variants and survival. In patients with GSTM1 null genotype and p53 Arg/Pro heterozygotes or Pro/Pro homozygotes the chance of survival is significantly lower than in the case of GSTM1+ and p53 Arg/Arg variants (p=0.009 and p=0.008, respectively). Conclusion: The significance of the investigated polymorphisms in prognosis is dependent on the tumor stage. These parameters might be used in certain cases as prognostic biomarkers in clinical diagnostics and in the planning of individual therapy. Copyright{\textcopyright} 2008 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved}, issn = {0250-7005}, URL = {https://ar.iiarjournals.org/content/28/3B/1917}, eprint = {https://ar.iiarjournals.org/content/28/3B/1917.full.pdf}, journal = {Anticancer Research} }