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Genetic analysis of long-term Barrett's esophagus epithelial cultures exhibiting cytogenetic and ploidy abnormalities

Identifieur interne : 003B67 ( Main/Exploration ); précédent : 003B66; suivant : 003B68

Genetic analysis of long-term Barrett's esophagus epithelial cultures exhibiting cytogenetic and ploidy abnormalities

Auteurs : M. Corinna Palanca-Wessels ; Michael T. Barrett [États-Unis] ; Patricia C. Galipeau [États-Unis] ; Katherine L. Rohrer ; Brian J. Reid [États-Unis] ; Peter S. Rabinovitch

Source :

Gastroenterology [ 0016-5085 ] ; 1998.

RBID : ISTEX:EC95A0E42D9807833CC1B92AD33B2BED56B5AC33

English descriptors

Abstract

Abstract: Background & Aims: Progression to cancer in Barrett's esophagus occurs through an accumulation of cell cycle and genetic abnormalities that have been documented in vivo. To better study neoplastic evolution in Barrett's esophagus, the aim of this study was to establish in vitro cultures from preneoplastic tissues. Methods: Mechanical and enzymatic dissociation methods were used to initiate Barrett's epithelial cultures from endoscopic biopsy specimens, and the cells were characterized using flow-cytometric, cytogenetic, and molecular genetic analyses. Results: Four long-term cultures were established from 39 attempts. All cultures contain cytogenetic abnormalities and elevated flow-cytometric 4N DNA content fractions. Molecular genetic abnormalities detected include the following: 9p and/or CDKN2/p16 abnormalities in 4 of 4 cultures, 17p loss of heterozygosity and p53 mutation in 3 of 4 cultures, and 5q loss of heterozygosity in 1 of 4 cultures. Inactivation of p53 was statistically associated with successful long-term culture. Conclusions: These cultures contain cell cycle and molecular genetic abnormalities that closely parallel those previously documented to occur early in cancer development in Barrett's esophagus in vivo. These alterations also appear to be associated with successful growth in vitro. The cultures may provide a premalignant in vitro system in which to test potential therapies for Barrett's esophagus as well as to examine etiologic factors and genetic intermediates important in neoplastic progression. GASTROENTEROLOGY 1998;114:295-304

Url:

https://api.istex.fr/ark:/67375/6H6-VD0GJZPJ-X/fulltext.pdf

DOI: 10.1016/S0016-5085(98)70480-9

Affiliations:

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Le document en format XML

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<term>Culture medium</term>
<term>Cultured cells</term>
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<term>Cytoplasmic enlargement</term>
<term>Deletion</term>
<term>Dicentric chromosomes</term>
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<term>Dysplasia</term>
<term>Early passage</term>
<term>Endoscopic</term>
<term>Endoscopic biopsy specimens</term>
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<term>Vivo biopsy specimens</term>
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<front><div type="abstract" xml:lang="en">Abstract: Background & Aims: Progression to cancer in Barrett's esophagus occurs through an accumulation of cell cycle and genetic abnormalities that have been documented in vivo. To better study neoplastic evolution in Barrett's esophagus, the aim of this study was to establish in vitro cultures from preneoplastic tissues. Methods: Mechanical and enzymatic dissociation methods were used to initiate Barrett's epithelial cultures from endoscopic biopsy specimens, and the cells were characterized using flow-cytometric, cytogenetic, and molecular genetic analyses. Results: Four long-term cultures were established from 39 attempts. All cultures contain cytogenetic abnormalities and elevated flow-cytometric 4N DNA content fractions. Molecular genetic abnormalities detected include the following: 9p and/or CDKN2/p16 abnormalities in 4 of 4 cultures, 17p loss of heterozygosity and p53 mutation in 3 of 4 cultures, and 5q loss of heterozygosity in 1 of 4 cultures. Inactivation of p53 was statistically associated with successful long-term culture. Conclusions: These cultures contain cell cycle and molecular genetic abnormalities that closely parallel those previously documented to occur early in cancer development in Barrett's esophagus in vivo. These alterations also appear to be associated with successful growth in vitro. The cultures may provide a premalignant in vitro system in which to test potential therapies for Barrett's esophagus as well as to examine etiologic factors and genetic intermediates important in neoplastic progression. GASTROENTEROLOGY 1998;114:295-304</div>
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Genetic analysis of long-term Barrett's esophagus epithelial cultures exhibiting cytogenetic and ploidy abnormalities

Genetic analysis of long-term Barrett's esophagus epithelial cultures exhibiting cytogenetic and ploidy abnormalities

Source :

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

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