The TP53 gene has been extensively studied in patients with chronic myeloid leukemia (CML), both in chronic phase and in blast crisis. Mutations in the gene were found in up to 30% of the patients, especially among those in blast crisis. We report the results of an analysis of 29 blood samples from
Molecular analysis of the TP53 gene in Barrett's adenocarcinoma
✍ Scribed by M.-P. Audrézet; M. Robaszkiewicz; B. Mercier; J.-B. Nousbaum; E. Hardy; J.-P. Bail; A. Volant; P. Lozac'h; H. Gouérou; C. Férec
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 468 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1059-7794
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✦ Synopsis
Communicated by Jean-Chude Kaphn
The TP53 gene is the most frequently mutated gene in human cancers. Barrett's esophagus provides an excellent model by which to understand the genetic evc:nts that lead from dysplasia to cancer. We screened for mutations in the TP53 gene by a combination of denaturing gradient gel electrophoresis and DNA sequencing in ten cases of adenocarcinoma arising in Barrett's mucosa. We have identified missense mutations in five of the ten samples, three transitions (R282W, G2455, R248W) and two transversions (E286Q and C176F). In one case we have analyzed biopsy specimens taken from the same site, one year before the patient developed an intra mucosal carcinoma. T h e mutation that was identified in this high grade dysplastic area was identical to that detected in the cancer. This would suggest TP53 mutations occur as an early genetic event in the development of Barrett's adenocarcinoma. 0 19% Wiley-Lisa, Inc.
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