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Low levels of apoptosis and proliferative activity in colorectal villous tumors: Comparison with tubular tumors

In order to clarlfy the cell kinetics of colorectal villous tumors (VT), 21 villous adenomatous areas and 12 carcinomatous areas within villous adenomas were investigated for proliferative activity and apoptosis and compared with a series of 41 tubular tumors (TT), demonstrating elements of intramuc...

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Bibliographic Details
Published in:Pathology international 1998-06, Vol.48 (6), p.453-459
Main Authors: IKENAGA, MAKOTO, TAKANO, YASUO, OHTANI, YOSHIMASA, TSUKAMOTO, HIDETO, HIKI, YOSHIKI, KAKITA, AKIRA, OKAYASU, LSAO
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Language:English
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Summary:In order to clarlfy the cell kinetics of colorectal villous tumors (VT), 21 villous adenomatous areas and 12 carcinomatous areas within villous adenomas were investigated for proliferative activity and apoptosis and compared with a series of 41 tubular tumors (TT), demonstrating elements of intramucosal carcinomas as well as tubular adenomas (so‐called carcinoma in tubular adenoma). Proliferation was estimated in terms of KI‐67 labeling indices and mitotic indices, and apoptosis was assessed by DNA nick‐end labeling to give apoptotic Indices. Apoptotic indices of villous adenomatous and carcinomatous regions were significantly lower than the values for their tubular counterparts. Kl‐67 labeling indices were also significantly lower for adenoma components. Apoptotic indices, Ki‐67 labeling indices and mitotic Indices increased with atypia raised in tubular adenoma components. Correlations of mitotic indices with apoptotic indices, Ki‐67 labeling Indices with apoptotic indices and mitotic Indices with Ki‐67 labeling indices were found for each villous tumor group and tubular tumor group, and the apoptosis and proliferation ratios for villous tumors were relatively low, suggesting a tendency for greater growth due to less cell deletion. Although this is only one of the biological features of villous tumor groups, it might play a major role in generation of malignancy.
ISSN:1320-5463
1440-1827
DOI:10.1111/j.1440-1827.1998.tb03932.x