Thymidylate synthase polymorphisms and mRNA expression are independent chemotherapy predictive markers in esophageal adenocarcinoma patients

• Published in: International journal of oncology Vol. 32; no. 1; pp. 201 - 208
• Main Authors: KURAMOCHI, Hidekazu, TANAKA, Koji, DANENBERG, Peter V, OH, Daniel, LEHMAN, Bethany J, DUNST, Christy M, DONG YUN YANG, DE MEESTER, Steven R, HAGEN, Jeffery A, DANENBERG, Kathleen D, DE MEESTER, Tom R
• Format: Journal Article
• Language: English
• Published: Athens Editorial Academy of the International Journal of Oncology 2008
• Subjects: 3' Untranslated Regions - genetics; 5' Untranslated Regions - genetics; Adenocarcinoma - drug therapy; Adenocarcinoma - genetics; Adult; Aged; Biological and medical sciences; Esophageal Neoplasms - drug therapy; Esophageal Neoplasms - genetics; Esophagus; Female; Gastroenterology. Liver. Pancreas. Abdomen; Genotype; Humans; Loss of Heterozygosity; Male; Medical sciences; Middle Aged; Polymorphism, Genetic; Prognosis; RNA, Messenger - analysis; Thymidylate Synthase - genetics; Tumors; Human; Genetic variability; Enzyme; Transferases; Esophageal disease; Biological marker; Genotype; Malignant tumor; Gene expression; Thymidylate synthase; Esophagus cancer; Chemotherapy; Treatment; Cancerology; Messenger RNA; Methyltransferases; esophageal adenocarcinoma; Digestive diseases; Esophagus adenocarcinoma; Cancer; Polymorphism
• ISSN: 1019-6439; 1791-2423
• DOI: 10.3892/ijo.32.1.201

Thymidylate synthase (TS) is known to have polymorphisms in the 5' and 3' untranslated region (UTR). These polymorphisms have been reported to be associated with high TS expression and chemoresistance to 5-FU. The aim of this study was to examine the prognostic roles of the 5'-UTR and 3'-UTR TS polymorphisms in esophageal adenocarcinoma patients, as well as their relation with TS mRNA expression. Eighty-three patients with esophageal adenocarcinoma were assessed. Thirty-four had received 5-FU containing chemotherapy and 49 were treated with surgery alone. Surgically resected tumor tissues were analyzed for TS genotype and TS mRNA expression using a quantitative real-time RT-PCR method. No survival difference was seen between the patients with 3RG allele (3RG group) and non-3RG group among surgery-alone patients. However, among patients with a history of 5-FU-based chemotherapy, the non-3RG group showed significantly better overall survival compared to the 3RG group (p=0.02). Moreover, whereas chemotherapy produced a significant increase in survival for the non-3RG group patients, those in the 3RG group obtained no survival benefit from chemotherapy. When patients were classified by low or high TS mRNA expression levels, low TS expressers obtained survival benefit from chemotherapy while high TS expressers did not, although there was no difference of median TS mRNA levels between 3RG and non-3RG group. The 3'-UTR polymorphism was not associated with overall survival. These results suggest that the status of the TS 5'-UTR polymorphism and TS mRNA expression are independent predictive markers for survival benefit from 5-FU-based therapy.