Literature DB >> 2616547

Barrett's esophagus: a model premalignant lesion for adenocarcinoma.

H S Garewal1, R Sampliner.   

Abstract

Barrett's esophagus is a condition in which the lower esophagus is lined with metaplastic columnar epithelium rather than normal stratified squamous epithelium. It is associated with an increased risk of cancer. Cancers developing in Barrett's epithelium are adenocarcinomas rather than the usual squamous cell esophageal cancers. Barrett's is somewhat unique among premalignant lesions, since it represents an entirely different epithelium from the normal and can therefore be histologically identified with certainty. The abnormal mucosa can be safely accessed repeatedly and its extent quantitated by endoscopy, thereby allowing serial follow-up studies and intervention trials. We are studying Barrett's esophagus as a model premalignant lesion for adenocarcinoma. Ornithine decarboxylase activity was increased in this lesion especially when dysplastic changes were present. Interestingly there was no relationship between polyamine levels and the increased ODC activity. Flow cytometric abnormalities have been demonstrated in Barrett's mucosa. Their significance remains to be determined. Epithelial cells from this lesion have been cultured and characterized. Clonal cytogenetic abnormalities were detected in some specimens. The cultured cells were used to test the effect of drugs on their growth. The ornithine decarboxylase inhibitor, alpha-difluoromethylornithine, significantly inhibited growth even at low concentrations. A clinical intervention trial using 13-cis-retinoic acid has produced no change in the extent of the lesion in 11 evaluable patients. Nevertheless, the successful performance of this clinical study confirms that this lesion can be used for intervention trials aimed at reversing premalignant lesions.

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Year:  1989        PMID: 2616547     DOI: 10.1016/0091-7435(89)90046-7

Source DB:  PubMed          Journal:  Prev Med        ISSN: 0091-7435            Impact factor:   4.018


  6 in total

1.  Flow cytometry in Barrett's esophagus. What have we learned so far?

Authors:  H S Garewal; R E Sampliner; M B Fennerty
Journal:  Dig Dis Sci       Date:  1991-05       Impact factor: 3.199

2.  Epidermal growth factor receptor overexpression and trisomy 7 in a case of Barrett's esophagus.

Authors:  H Garewal; P Meltzer; J Trent; R Prabhala; R Sampliner; M Korc
Journal:  Dig Dis Sci       Date:  1990-09       Impact factor: 3.199

3.  Recent developments in Barrett's esophagus.

Authors:  H S Garewal
Journal:  Curr Oncol Rep       Date:  2000-05       Impact factor: 5.075

4.  Upregulation of ornithine decarboxylase mRNA expression in Barrett's esophagus and Barrett's-associated adenocarcinoma.

Authors:  J Brabender; R V Lord; K D Danenberg; R Metzger; P M Schneider; H Uetake; K Kawakami; J M Park; D Salonga; J H Peters; T R DeMeester; A H Hölscher; P V Danenberg
Journal:  J Gastrointest Surg       Date:  2001 Mar-Apr       Impact factor: 3.452

5.  Adenocarcinoma of the esophagus and esophagogastric junction in white men in the United States: alcohol, tobacco, and socioeconomic factors.

Authors:  L M Brown; D T Silverman; L M Pottern; J B Schoenberg; R S Greenberg; G M Swanson; J M Liff; A G Schwartz; R B Hayes; W J Blot
Journal:  Cancer Causes Control       Date:  1994-07       Impact factor: 2.506

6.  Immunohistochemical expression of ornithine decarboxylase, diamine oxidase, putrescine, and spermine in normal canine enterocolic mucosa, in chronic colitis, and in colorectal cancer.

Authors:  Giacomo Rossi; Matteo Cerquetella; Graziano Pengo; Subeide Mari; Emilia Balint; Gabrio Bassotti; Nicolae Manolescu
Journal:  Biomed Res Int       Date:  2015-10-15       Impact factor: 3.411

  6 in total

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