Review
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Dec 15, 2003; 9(12): 2635-2641
Published online Dec 15, 2003. doi: 10.3748/wjg.v9.i12.2635
Reg gene family and human diseases
Yu-Wei Zhang, Liu-Song Ding, Mao-De Lai
Yu-Wei Zhang, Department of Pathology, School of Medicine, Zhejiang University, Hangzhou 310006, Zhejiang Province, China and Department of Pathology, School of Basic Medical Sciences, Southeast University, Nanjing 210009, Jiangsu Province, China
Mao-De Lai, Department of Pathology, School of Medicine, Zhejiang University, Hangzhou 310006, Zhejiang Province, China
Liu-Song Ding, Zhejiang University Libraries, Hangzhou 310006, Zhejiang Province, China
Author contributions: All authors contributed equally to the work.
Supported by National Natural Science Foundation of China, No. 30200333 and No.30371605
Correspondence to: Dr. Yu-Wei Zhang, Department of Pathology, School of Basic Medical Sciences, Southeast University, Nanjing 210009, Jiangsu Province, China. yuwei123@seu.edu.cn
Telephone: +86-571-87217134 Fax: +86-571-87951358
Received: May 10, 2003
Revised: May 16, 2003
Accepted: June 2, 2003
Published online: December 15, 2003
Abstract

Regenerating gene (Reg or REG) family, within the superfamily of C-type lectin, is mainly involved in the liver, pancreatic, gastric and intestinal cell proliferation or differentiation. Considerable attention has focused on Reg family and its structurally related molecules. Over the last 15 years, 17 members of the Reg family have been cloned and sequenced. They have been considered as members of a conserved protein family sharing structural and some functional properties being involved in injury, inflammation, diabetes and carcinogenesis. We previously identified Reg IV as a strong candidate for a gene that was highly expressed in colorectal adenoma when compared to normal mucosa based on suppression subtractive hybridization (SSH), reverse Northern blot, semi-quantitative reverse transcriptase PCR (RT-PCR) and Northern blot. In situ hybridization results further support that overexpression of Reg IV may be an early event in colorectal carcinogenesis. We suggest that detection of Reg IV overexpression might be useful in the early diagnosis of carcinomatous transformation of adenoma. This review summarizes the roles of Reg family in diseases in the literature as well as our recent results of Reg IV in colorectal cancer. The biological properties of Reg family and its possible roles in human diseases are discussed. We particularly focus on the roles of Reg family as sensitive reactants of tissue injury, prognostic indicators of tumor survival and early biomarkers of carcinogenesis. In addition to our current understanding of Reg gene functions, we postulate that there might be relationships between Reg family and microsatellite instability, apoptosis and cancer with a poor prognosis. Investigation of the correlation between tumor Reg expression and survival rate, and analysis of the Reg gene status in human maliganancies, are required to elucidate the biologic consequences of Reg gene expression, the implications for Reg gene regulation of cell growth, tumorigenesis, and the progression of cancer. It needs to be further attested whether Reg gene family is applicable in early detection of cancer and whether Reg and Reg-related molecules can offer novel molecular targets for anticancer therapeutics. This has implications with regard to prognosis, such as in monitoring cancer initiation, progression and recurrence, as well as the design of chemotherapeutic drugs.

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