Literature DB >> 8033325

Resistance of aberrant crypt foci to apoptosis induced by azoxymethane in rats chronically fed cholic acid.

B A Magnuson1, N Shirtliff, R P Bird.   

Abstract

We have previously shown that chronic feeding of cholic acid to carcinogen treated rats reduces the number of putative preneoplastic lesions of colonic cancer, aberrant crypt foci (ACF), but enhances the growth of remaining ACF and the incidence of colonic tumors. The following study was conducted to further explore the effects of cholic acid on ACF growth by determining if ACF in cholic acid-fed animals display resistance to apoptotic cell death. ACF were induced in male Sprague-Dawley rats with two injections of azoxymethane (20 mg/kg body wt). Rats were divided into two groups and fed either the control AIN-76 diet or the AIN-76 diet containing 0.2% cholic acid. After 18 weeks, colonic apoptotic cell death was induced with an acute low dose of azoxymethane (10 mg/kg body wt). The number of cells, apoptotic bodies and bromodeoxyuridine (BUdR)-labeled cells were determined in colonic crypts comprising ACF and surrounding normal crypts in rats from each diet group. The number of apoptotic bodies per 100 cells was lower in ACF crypts than in normal-appearing crypts (P = 0.0034). Both normal and ACF crypts from rats fed the cholic acid diet had fewer apoptotic bodies per 100 cells than crypts from rats fed the control diet (P = 0.0102). These data suggest that ACF harbor resistance to induction of apoptosis. Chronic feeding of a diet containing 0.2% cholic acid results in the development of increased resistance to apoptosis. The lower rate of cell death in ACF may contribute to the enhanced growth of ACF and higher tumor incidence previously observed in cholic acid-fed animals.

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Year:  1994        PMID: 8033325     DOI: 10.1093/carcin/15.7.1459

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  9 in total

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

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4.  Anti-apoptotic phenotypes of cholestan-3β,5α,6β-triol-resistant human cholangiocytes: characteristics contributing to the genesis of cholangiocarcinoma.

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

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

Authors:  Claire M Payne; Carol Bernstein; Katerina Dvorak; Harris Bernstein
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8.  Comparison of the composition of bile acids in bile of patients with adenocarcinoma of the pancreas and benign disease.

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Journal:  J Steroid Biochem Mol Biol       Date:  2017-10-12       Impact factor: 4.292

Review 9.  Role of bile acids in carcinogenesis of pancreatic cancer: An old topic with new perspective.

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  9 in total

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