Literature DB >> 7571081

Role of apoptosis in biology and pathology: resistance to apoptosis in colon carcinogenesis.

C M Payne1, H Bernstein, C Bernstein, H Garewal.   

Abstract

The overview of apoptosis presented here emphasizes cell deletion in the immune system, with particular reference to T- and B-lymphocyte development, and the in vivo and in vitro senescence of human neutrophils. Some biochemical criteria that are used to identify apoptotic cells are described. Pitfalls in using agarose gel electrophoresis as the sole method for the identification of apoptotic cells are discussed. There are multiple modes of cell death that can be identified at the morphologic level. Thus the central role of microscopic methods, and in particular, electron microscopy, as an important tool in the study of cell death mechanisms, is presented. Apoptosis has a protective role against disease and could, a priori, have an important role in either the initiation or progression of cancer. Two paradoxes concerning the relationship of tumor aggressiveness at the clinical level to mitotic activity have been explained by an evaluation of apoptotic index. In the first case, basal cell carcinomas grow slowly but show a high rate of mitosis. Here, the apoptotic rate is quite high, but just below the mitotic rate, thereby accounting for the slow rate of growth. A second instance is follicular lymphoma, which has a low rate of mitosis that is less than that described for reactive germinal centers. However, apoptosis is markedly reduced in follicular lymphomas compared with that seen in reactive germinal centers, thus providing an explanation for the progressive growth of the follicle. We present a brief description of recent work from our laboratory that indicates that apoptosis may play an important role in colon carcinogenesis. We have shown that sodium deoxycholate, the particular bile salt present in highest concentration in the colon, induces apoptosis in the goblet cells of the human colonic mucosa in an in vitro assay. The intriguing finding is that cells of the normal-appearing mucosa of colon cancer patients are resistant to bile salt-induced apoptosis. This suggests a novel hypothesis about the etiologic role of bile salts in colon cancer. The chronic presence of bile salts that accompany a high-fat diet could select for apoptosis-resistant epithelial cells in the colon over time. Thus, a resistance-to-apoptosis bioassay may prove useful as an intermediate biomarker for determining which individuals are at high risk for colon cancer.

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Year:  1995        PMID: 7571081     DOI: 10.3109/01913129509064227

Source DB:  PubMed          Journal:  Ultrastruct Pathol        ISSN: 0191-3123            Impact factor:   1.094


  16 in total

1.  Molecular and cellular pathways associated with chromosome 1p deletions during colon carcinogenesis.

Authors:  Claire M Payne; Cheray Crowley-Skillicorn; Carol Bernstein; Hana Holubec; Harris Bernstein
Journal:  Clin Exp Gastroenterol       Date:  2011-05-03

Review 2.  Aberrant crypt foci in colorectal carcinogenesis. Cell and crypt dynamics.

Authors:  L Roncucci; M Pedroni; F Vaccina; P Benatti; L Marzona; A De Pol
Journal:  Cell Prolif       Date:  2000-02       Impact factor: 6.831

3.  Bile acids in combination with low pH induce oxidative stress and oxidative DNA damage: relevance to the pathogenesis of Barrett's oesophagus.

Authors:  Katerina Dvorak; Claire M Payne; Melissa Chavarria; Lois Ramsey; Barbora Dvorakova; Harris Bernstein; Hana Holubec; Richard E Sampliner; Naihsuan Guy; Amanda Condon; Carol Bernstein; Sylvan B Green; Anil Prasad; Harinder S Garewal
Journal:  Gut       Date:  2006-12-04       Impact factor: 23.059

4.  Effect of resistant starch on potential biomarkers for colonic cancer risk in patients with colonic adenomas: a controlled trial.

Authors:  M J Grubben; C C van den Braak; M Essenberg; M Olthof; A Tangerman; M B Katan; F M Nagengast
Journal:  Dig Dis Sci       Date:  2001-04       Impact factor: 3.199

Review 5.  Field defects in progression to gastrointestinal tract cancers.

Authors:  Carol Bernstein; Harris Bernstein; Claire M Payne; Katerina Dvorak; Harinder Garewal
Journal:  Cancer Lett       Date:  2007-12-31       Impact factor: 8.679

6.  Physical activity as a determinant of fecal bile acid levels.

Authors:  Betsy C Wertheim; María Elena Martínez; Erin L Ashbeck; Denise J Roe; Elizabeth T Jacobs; David S Alberts; Patricia A Thompson
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2009-04-21       Impact factor: 4.254

7.  Bile acids as endogenous etiologic agents in gastrointestinal cancer.

Authors:  Harris Bernstein; Carol Bernstein; Claire M Payne; Katerina Dvorak
Journal:  World J Gastroenterol       Date:  2009-07-21       Impact factor: 5.742

8.  Bile salt-induced apoptosis in human colon cancer cell lines involves the mitochondrial transmembrane potential but not the CD95 (Fas/Apo-1) receptor.

Authors:  Frank-Peter Wachs; René C Krieg; Cecilia M P Rodrigues; Helmut Messmann; Frank Kullmann; Ruth Knüchel-Clarke; Jürgen Schölmerich; Gerhard Rogler; Klaus Schlottmann
Journal:  Int J Colorectal Dis       Date:  2004-09-07       Impact factor: 2.571

9.  Hydrophobic bile acids, genomic instability, Darwinian selection, and colon carcinogenesis.

Authors:  Claire M Payne; Carol Bernstein; Katerina Dvorak; Harris Bernstein
Journal:  Clin Exp Gastroenterol       Date:  2008-12-16

10.  The Na+/H+ exchanger controls deoxycholic acid-induced apoptosis by a H+-activated, Na+-dependent ionic shift in esophageal cells.

Authors:  Aaron Goldman; HwuDauRw Chen; Mohammad R Khan; Heather Roesly; Kimberly A Hill; Mohammad Shahidullah; Amritlal Mandal; Nicholas A Delamere; Katerina Dvorak
Journal:  PLoS One       Date:  2011-08-22       Impact factor: 3.240

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