Rapid Communication
Copyright ©2007 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Mar 14, 2007; 13(10): 1612-1617
Published online Mar 14, 2007. doi: 10.3748/wjg.v13.i10.1612
Clinical and molecular analysis of hereditary non-polyposis colorectal cancer in Chinese colorectal cancer patients
Jun Wang, Mao-Hong Luo, Zuo-Xing Zhang, Pei-Da Zhang, Xi-Li Jiang, Dong-Wang Ma, Rong-Zeng Suo, Li-Zhong Zhao, Qing-Hui Qi
Jun Wang, Hereditary Colorectal Tumors Registry and Tianjin Binjiang Hospital, Tianjin 300022, China
Mao-Hong Luo, Hereditary Colorectal Tumors Registry, Tianjin, China and Tianjin Medical University, Tianjin 300022, China
Zuo-Xing Zhang, Pei-Da Zhang, Xi-Li Jiang, Rong-Zeng Suo, Li-Zhong Zhao, Dong-Wang MA, Tianjin Binjiang Hospital, Tianjin 300022, China
Qing-Hui Qi, Tianjin Medical University Hospital, Tianjin, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Jun Wang, Hereditary Colorectal Tumors Registry, Binjiang Road 205, Heping district, Tianjin 300022, China. chinahcc@vip.sina.com
Telephone: +86-22-27111390 Fax: +86-22-27121297
Received: October 26, 2006
Revised: December 1, 2006
Accepted: February 14, 2007
Published online: March 14, 2007
Abstract

AIM: To analyze the frequency of hereditary non-polyposis colorectal cancer (HNPCC) in Chinese colorectal cancer (CRC) patients, and to discuss the value of microsatellite instability (MSI) and/or immunohistochemistry (IHC) for MSH2/MLH1 protein analysis as pre-screening tests in China.

METHODS: The Amsterdam criteriaIandII(clinical diagnosis) and/or germline hMLH1/hMSH2 mutations (genetic diagnosis) were used to classify HNPCC families. Genetic tests, including microsatellite instability, immunohistochemistry for MSH2/MLH1 proteins and hMSH2/hMLH1 genes, were performed in each proband.

RESULTS: From July 2000 to June 2004, 1988 patients with colorectal cancer were analysed and 114 CRC patients (5.7%) from 48 families were categorized as having HNPCC, including 76 from 26 families diagnosed clinically and 38 from the other 22 families diagnosed genetically. The sensitivity and specificity of high MSI and IHC for predicting mutations were 100% and 54%, and 79% and 77%, respectively.

CONCLUSION: The frequency of HNPCC is approximately 10% among all Chinese CRC cases. The MSI and IHC detections for hMSH2/hMLH1 proteins are reliable pre-screening tests for hMLH1/hMSH2 germline mutations in families suspected of having HNPCC.

Keywords: Hereditary non-polyposis colorectal cancer, Colorectal cancer, Mismatch repair gene, Immunohistochemistry, Microsatellite instability