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Usefulness of proliferative activity, DNA ploidy pattern and p53 products as diagnostic adjuncts in colorectal adenomas and intramucosal carcinomas
Author(s) -
Sugai Tamotsu,
Nakamura Shinichi,
Habano Wataru,
Uesugi Noriyuki,
Sato Hajime,
Yoshida Toru,
Orii Seishi
Publication year - 1999
Publication title -
pathology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
eISSN - 1440-1827
pISSN - 1320-5463
DOI - 10.1046/j.1440-1827.1999.00914.x
Subject(s) - pathology , aneuploidy , immunohistochemistry , stain , staining , adenoma , carcinoma , ki 67 , biology , colorectal cancer , medicine , cancer , chromosome , biochemistry , gene
Although numerous studies have assessed the biologic parameters of tumors, measurement of these parameters has had, to date, little impact on histologic diagnosis. Furthermore, analysis of a single parameter is insufficient to evaluate tumor malignant potential. In the present study, cell proliferation, DNA ploidy and p53 product were analyzed to objectify the tumor malignant potential in colorectal adenomas and intramucosal carcinomas. Sixty‐one adenomas and 49 intramucosal carcinomas were studied using immunohistochemical analysis of Ki‐67 and p53, silver‐staining nucleolar organizer region (AgNOR) stain and DNA ploidy in fresh samples. Intramucosal carcinoma exhibited a greater Ki‐67‐positive rate and AgNOR count than the adenomas, although these parameters varied widely among samples. The incidence of aneuploidy and p53 over‐expression in colorectal intramucosal carcinomas was significantly higher than in colorectal adenomas. These results indicate that DNA aneuploidy and p53 accumulation are the most reliable parameters for distinguishing benign and malignant lesions.