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p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas.

The p53 gene is one of the best studied tumour suppressor genes. Recently we performed mutation analysis on the p53 gene in a large number of bone and soft tissue sarcomas, and found that approximately one-third of the sarcomas have some type of DNA alteration at the p53 locus (Toguchida et al., 199...

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Autores principales: Wadayama, B., Toguchida, J., Yamaguchi, T., Sasaki, M. S., Yamamuro, T.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968651/
https://www.ncbi.nlm.nih.gov/pubmed/8260365
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author Wadayama, B.
Toguchida, J.
Yamaguchi, T.
Sasaki, M. S.
Yamamuro, T.
author_facet Wadayama, B.
Toguchida, J.
Yamaguchi, T.
Sasaki, M. S.
Yamamuro, T.
author_sort Wadayama, B.
collection PubMed
description The p53 gene is one of the best studied tumour suppressor genes. Recently we performed mutation analysis on the p53 gene in a large number of bone and soft tissue sarcomas, and found that approximately one-third of the sarcomas have some type of DNA alteration at the p53 locus (Toguchida et al., 1992). However, the expression of the p53 protein resulting from these alterations still remains to be clarified. In this study, p53 expression in the sarcoma tissues was analysed immunohistochemically using antibody PAb421 (Oncogene Science) and its relationship to DNA alterations was examined. Of 113 tumours, 29 (25.7%) showed positive staining for the p53 protein. These included 19 of 67 osteosarcomas, five of 20 chondrosarcomas, four of 11 malignant fibrous histiocytomas (MFHs) and one Ewing's sarcoma. In chondrosarcomas, most of the p53-positive tumours belonged to highly malignant and atypical tumour types (dedifferentiated or mesenchymal type), suggesting a role for p53 mutation in the progression of cartilaginous tumours. All the cases with a missense mutation showed strongly positive staining, while no immunoreactivity was observed in the remaining three-quarters with DNA alterations including gross rearrangement, frame-shift mutation, nonsense mutation or mutation at splicing site except in one case. These results demonstrated the dominance of the p53 mutations with null protein expression in bone and soft tissue sarcomas, showing a unique characteristic of these types of tumours compared with other malignancies such as colon carcinomas. IMAGES:
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spelling pubmed-19686512009-09-10 p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas. Wadayama, B. Toguchida, J. Yamaguchi, T. Sasaki, M. S. Yamamuro, T. Br J Cancer Research Article The p53 gene is one of the best studied tumour suppressor genes. Recently we performed mutation analysis on the p53 gene in a large number of bone and soft tissue sarcomas, and found that approximately one-third of the sarcomas have some type of DNA alteration at the p53 locus (Toguchida et al., 1992). However, the expression of the p53 protein resulting from these alterations still remains to be clarified. In this study, p53 expression in the sarcoma tissues was analysed immunohistochemically using antibody PAb421 (Oncogene Science) and its relationship to DNA alterations was examined. Of 113 tumours, 29 (25.7%) showed positive staining for the p53 protein. These included 19 of 67 osteosarcomas, five of 20 chondrosarcomas, four of 11 malignant fibrous histiocytomas (MFHs) and one Ewing's sarcoma. In chondrosarcomas, most of the p53-positive tumours belonged to highly malignant and atypical tumour types (dedifferentiated or mesenchymal type), suggesting a role for p53 mutation in the progression of cartilaginous tumours. All the cases with a missense mutation showed strongly positive staining, while no immunoreactivity was observed in the remaining three-quarters with DNA alterations including gross rearrangement, frame-shift mutation, nonsense mutation or mutation at splicing site except in one case. These results demonstrated the dominance of the p53 mutations with null protein expression in bone and soft tissue sarcomas, showing a unique characteristic of these types of tumours compared with other malignancies such as colon carcinomas. IMAGES: Nature Publishing Group 1993-12 /pmc/articles/PMC1968651/ /pubmed/8260365 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Wadayama, B.
Toguchida, J.
Yamaguchi, T.
Sasaki, M. S.
Yamamuro, T.
p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas.
title p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas.
title_full p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas.
title_fullStr p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas.
title_full_unstemmed p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas.
title_short p53 expression and its relationship to DNA alterations in bone and soft tissue sarcomas.
title_sort p53 expression and its relationship to dna alterations in bone and soft tissue sarcomas.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968651/
https://www.ncbi.nlm.nih.gov/pubmed/8260365
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