Literature DB >> 8417821

Expansion of the epithelial cell proliferative compartment and frequency of adenomatous polyps in the colon correlate with the strength of family history of colorectal cancer.

H Gerdes1, J S Gillin, E Zimbalist, C Urmacher, M Lipkin, S J Winawer.   

Abstract

Expansion of the proliferative compartment of epithelial cells in colonic crypts and colonic adenomas have been described as phenotypic precursors to colon cancer in individuals affected with hereditary or sporadic colon cancer. This study measured the size of the proliferative compartment in colonic crypts and the frequency of adenomas in asymptomatic members of families having sporadic colorectal cancer. The subjects were divided into 2 groups according to the frequency of colorectal cancer in their families. A shift of the compartment of proliferating epithelial cells toward the lumenal surface of colonic crypts was seen in the group of subjects with a stronger family history of colorectal cancer, with significant differences in the numbers of proliferative cells in the upper and the lower crypt compartments (P < 0.05) and in the fraction of proliferative cells at the highest compartment at the lumenal surface of the crypts (P < 0.05). Cell proliferation patterns in normal-appearing mucosa of the 2 groups revealed no difference in whole crypt [3H]thymidine labeling index. Colonoscopic examination of the 56 subjects revealed an overall prevalence of adenomas of 21%; when stratified by frequency of colorectal cancer in their families, 3 of 22 subjects (14%) with a weaker family history had adenomas, while 9 of 34 (26%) with a stronger family history had adenomas. Thus, parallel abnormalities of colonic epithelial cell proliferation and neoplasia were seen in individuals with a family history of colorectal cancer, both of which were more pronounced with increasing strength of family history. This observation provides further evidence of relationships among these factors in the etiology of "sporadic" colorectal cancer.

Entities:  

Mesh:

Year:  1993        PMID: 8417821

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  11 in total

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4.  Colonic crypt cell proliferation state assessed by whole crypt microdissection in sporadic neoplasia and familial adenomatous polyposis.

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5.  Semiparametric estimation for joint modeling of colorectal cancer risk and functional biomarkers measured with errors.

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6.  The genotype of the transporter associated with antigen processing gene affects susceptibility to colorectal cancer in Japanese.

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7.  Modeling clinical outcome using multiple correlated functional biomarkers: A Bayesian approach.

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8.  Proliferative compartment deregulation in the non-neoplastic colonic epithelium of familial adenomatous polyposis.

Authors:  S J Mills; N A Shepherd; P A Hall; A Hastings; J C Mathers; A Gunn
Journal:  Gut       Date:  1995-03       Impact factor: 23.059

9.  Growth, homeostatic regulation and stem cell dynamics in tissues.

Authors:  E Hannezo; J Prost; J-F Joanny
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10.  Effects of ginger supplementation on cell-cycle biomarkers in the normal-appearing colonic mucosa of patients at increased risk for colorectal cancer: results from a pilot, randomized, and controlled trial.

Authors:  Jessica Citronberg; Roberd Bostick; Thomas Ahearn; D Kim Turgeon; Mack T Ruffin; Zora Djuric; Ananda Sen; Dean E Brenner; Suzanna M Zick
Journal:  Cancer Prev Res (Phila)       Date:  2013-01-09
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