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Deletions of 9p21 and TP53 in bladder cancer.

The objective of this study was to characterize the alterations of 9p21 and TP53 in Korean transitional bladder cancer and to assess the relationship between the histopathologic parameter and the alteration of these genes. Allele loss in 29 surgically resected transitional cell carcinoma was examine...

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Detalles Bibliográficos
Autores principales: Park, W. S., Oh, M. J., Lee, H. K., Lee, K. O., Rhyu, M. G., Dong, S. M., Lee, J. Y., Kim, S. H.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054043/
https://www.ncbi.nlm.nih.gov/pubmed/8843005
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author Park, W. S.
Oh, M. J.
Lee, H. K.
Lee, K. O.
Rhyu, M. G.
Dong, S. M.
Lee, J. Y.
Kim, S. H.
author_facet Park, W. S.
Oh, M. J.
Lee, H. K.
Lee, K. O.
Rhyu, M. G.
Dong, S. M.
Lee, J. Y.
Kim, S. H.
author_sort Park, W. S.
collection PubMed
description The objective of this study was to characterize the alterations of 9p21 and TP53 in Korean transitional bladder cancer and to assess the relationship between the histopathologic parameter and the alteration of these genes. Allele loss in 29 surgically resected transitional cell carcinoma was examined by using the multiplex PCR with 7 and 1 microsatellite markers for 9p21 and TP53, respectively. Twenty-one (72%) demonstrated allele loss at 9p21 and/or TP53. Deletion at the 9p21 region was detected in 17(61%) of 28 informative cases at one or more loci, and LOH at TP53 was found in 12(55%) of 22 informative cases. Of 7 microsatellite markers for 9p21, allele loss occurred the most frequently at locus D9S162(69%) and D9S104(69%). Additionally, hemizygous deletion was slightly more common than homozygous deletion. Deletion at 9p21 and TP53 was not related with increased grade. These results suggest that the alteration of 9p21 may be an early event in the development of Korean bladder cancer, while p53 gene may be involved in early event of some bladder cancers as well as in their late events.
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spelling pubmed-30540432011-03-15 Deletions of 9p21 and TP53 in bladder cancer. Park, W. S. Oh, M. J. Lee, H. K. Lee, K. O. Rhyu, M. G. Dong, S. M. Lee, J. Y. Kim, S. H. J Korean Med Sci Research Article The objective of this study was to characterize the alterations of 9p21 and TP53 in Korean transitional bladder cancer and to assess the relationship between the histopathologic parameter and the alteration of these genes. Allele loss in 29 surgically resected transitional cell carcinoma was examined by using the multiplex PCR with 7 and 1 microsatellite markers for 9p21 and TP53, respectively. Twenty-one (72%) demonstrated allele loss at 9p21 and/or TP53. Deletion at the 9p21 region was detected in 17(61%) of 28 informative cases at one or more loci, and LOH at TP53 was found in 12(55%) of 22 informative cases. Of 7 microsatellite markers for 9p21, allele loss occurred the most frequently at locus D9S162(69%) and D9S104(69%). Additionally, hemizygous deletion was slightly more common than homozygous deletion. Deletion at 9p21 and TP53 was not related with increased grade. These results suggest that the alteration of 9p21 may be an early event in the development of Korean bladder cancer, while p53 gene may be involved in early event of some bladder cancers as well as in their late events. Korean Academy of Medical Sciences 1996-06 /pmc/articles/PMC3054043/ /pubmed/8843005 Text en
spellingShingle Research Article
Park, W. S.
Oh, M. J.
Lee, H. K.
Lee, K. O.
Rhyu, M. G.
Dong, S. M.
Lee, J. Y.
Kim, S. H.
Deletions of 9p21 and TP53 in bladder cancer.
title Deletions of 9p21 and TP53 in bladder cancer.
title_full Deletions of 9p21 and TP53 in bladder cancer.
title_fullStr Deletions of 9p21 and TP53 in bladder cancer.
title_full_unstemmed Deletions of 9p21 and TP53 in bladder cancer.
title_short Deletions of 9p21 and TP53 in bladder cancer.
title_sort deletions of 9p21 and tp53 in bladder cancer.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054043/
https://www.ncbi.nlm.nih.gov/pubmed/8843005
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