Esophageal Cancer
Copyright ©The Author(s) 2005. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 14, 2005; 11(30): 4618-4622
Published online Aug 14, 2005. doi: 10.3748/wjg.v11.i30.4618
Mutation of DNA polymerase β in esophageal carcinoma of different regions
Guo-Qiang Zhao, Tao Wang, Qin Zhao, Hong-Yan Yang, Xiao-Hui Tan, Zi-Ming Dong
Guo-Qiang Zhao, Tao Wang, Qin Zhao, Hong-Yan Yang, Xiao-Hui Tan, Zi-Ming Dong, Basic Medical College, Zhengzhou University, Zhengzhou 450052, Henan Province, China
Author contributions: All authors contributed equally to the work.
Supported by the National Natural Science Foundation of China, No. 39870287
Correspondence to: Dr. Guo-Qiang Zhao, Basic Medical College, Zhengzhou University, Zhengzhou 450052, Henan Province, China. zhaogq@zzu.edu.cn
Telephone: +86-371-66912523
Received: November 2, 2004
Revised: December 23, 2004
Accepted: December 26, 2004
Published online: August 14, 2005
Abstract

AIM: To observe the variation of DNA polymerase β (polβ) in esophageal carcinoma.

METHODS: Thirty specimens containing adjacent normal epithelial tissues were collected from patients in Linzhou region (a high risk area for esophageal squamous carcinoma) and 25 specimens were from a non-high risk area. Total RNA was extracted from the samples and reverse transcription polymerase chain reaction (RT-PCR) was performed. PCR products were cloned and sequenced to investigate the polβ gene with DNASIS and OMIGA. Statistical significance was evaluated using the χ2 test.

RESULTS: High-incidence area group: polβ gene variation was detected in 13 of 30 esophageal carcinoma tissue specimens, and only one variation was found in 30 corresponding adjacent normal tissue specimens. Non high-incidence area group: polβ gene variation was detected in 5 of 25 esophageal carcinoma tissue specimens, and no variation was found in 25 corresponding adjacent normal tissue specimens. The incidence of polβ gene variation observed in the high-incidence area group was significantly higher than in the non-high incidence area group. Two mutation hot spots (454-466 and 648-670 nt) and a 58 bp deletion (177-234 nt) were found.

CONCLUSION: Variations of polβ perform different functions between the high-incidence areas and the other areas, and may play a more important role in the high-incidence areas.

Keywords: DNA polymerase β; Esophageal carcinoma; Gene mutation