Abstract
Background: Mounting evidence indicates that alteration of apoptosis is involved in the mechanisms of cancer development. PUMA, a pro-apoptotic member of Bcl-2 family, mediates p53-dependent and -independent apoptosis. Aim: The aim of this study was to explore whether alteration of PUMA protein expression is a characteristic of human gastric carcinomas. Patients and methods: We analysed expression of PUMA protein in 60 gastric adenocarcinomas by immunohistochemistry. Also, we examined PUMA gene mutation in the same tissues by a single-strand conformation polymorphism. Results: PUMA protein expression was detected in 44 cases (73%) of the 60 gastric carcinomas, whereas it was not detected in normal gastric mucosal epithelial cells. The mutational analysis revealed no PUMA mutation in the gastric carcinomas. Conclusions: Our data suggest that PUMA mutation is not a direct target of inactivation in gastric tumourigenesis. Also, increased expression of PUMA in malignant gastric epithelial cells compared with normal mucosal epithelial cells suggested that PUMA expression may play a role in gastric tumourigenesis. © 2006 Editrice Gastroenterologica Italiana S.r.l.
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Yoo, N. J., Lee, J. W., Jeong, E. G., & Lee, S. H. (2007). Immunohistochemical analysis of pro-apoptotic PUMA protein and mutational analysis of PUMA gene in gastric carcinomas. Digestive and Liver Disease, 39(3), 222–227. https://doi.org/10.1016/j.dld.2006.11.006
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