Esophageal Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jun 15, 2003; 9(6): 1179-1181
Published online Jun 15, 2003. doi: 10.3748/wjg.v9.i6.1179
Expression of a plant-associated human cancer antigen in normal, premalignant and malignant esophageal tissues
Jun Fu, Ping Qu, Mo Li, Hai-Mei Tian, Zhen-Hai Zheng, Xin-Wen Zheng, Wei Zhang
Jun Fu, Ping Qu, Mo Li, Hai-Mei Tian, Wei Zhang, Central Laboratory for Tumor Biology, Cancer Hospital (Institute), Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, China
Zhen-Hai Zheng, Xin-Wen Zheng, Zheng's Cancer Institute, Linshou 050500, HeBei Province, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Professor Wei Zhang, Central Laboratory for Tumor Biology, Cancer Institute, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100021, China. zhangwe@public.bta.net.cn
Telephone: +86-10-67718679 Fax: +86-10-67718679
Received: December 24, 2002
Revised: March 1, 2003
Accepted: March 5, 2003
Published online: June 15, 2003
Abstract

AIM: To study the relationship between the expression profiles of a plant-associated human cancer antigen and carcinogenesis of esophagus and its significance.

METHODS: We analyzed expression of a plant-associated human cancer antigen in biopsy specimens of normal (n = 29), mildly hyperplastic (n = 29), mildly (n = 30), moderately (n = 27) and severely dysplastic (n = 29) and malignant esophageal (n = 30) tissues by immunohistochemistry.

RESULTS: The plant-associated human cancer antigen was mainly confined to the cytoplasm and showed diffuse type of staining. Positive staining was absent or weak in normal (0/30) and mildly hyperplastic tissue samples (2/29), while strong staining was observed in severe dysplasia (23/29) and carcinoma in situ (24/30). There was significant difference of its expression between normal mucosa and severely dysplastic tissues (P < 0.001) or carcinoma in situ (P < 0.001). Significant difference was also observed between mild dysplasia and severe dysplasia (P < 0.001) or carcinoma in situ (P < 0.001). An overall trend toward increased staining intensity with increasing grade of dysplasia was found. There was a linear correlation between grade of lesions and staining intensity (r = 0.794, P < 0.001). Samples from esophageal cancer showed no higher levels of expression than those in severely dysplastic lesions (P > 0.05).

CONCLUSION: The abnormal expression of this plant-associated human cancer antigen in esophageal lesions is a frequent and early finding in the normal-dysplasia-carcinoma sequence in esophageal carcinogenesis. It might contribute to the carcinogenesis of esophageal cancer. The abnormal expression of this plant-associated human cancer antigen in esophageal lesion tissues may serve as a potential new biomarker for early identification of esophageal cancer.

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