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Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter.

Cyclin E gene alteration in the cell cycle plays an important role in carcinogenesis, while p53 protein affects different phase checkpoint pathways by activating p21WAF1/CIP1 in the normal cell cycle. We immunohistochemically examined the expression of cyclin E and p53 proteins in 121 patients with...

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Autores principales: Furihata, M., Ohtsuki, Y., Sonobe, H., Shuin, T., Yamamoto, A., Terao, N., Kuwahara, M.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2149960/
https://www.ncbi.nlm.nih.gov/pubmed/9514058
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author Furihata, M.
Ohtsuki, Y.
Sonobe, H.
Shuin, T.
Yamamoto, A.
Terao, N.
Kuwahara, M.
author_facet Furihata, M.
Ohtsuki, Y.
Sonobe, H.
Shuin, T.
Yamamoto, A.
Terao, N.
Kuwahara, M.
author_sort Furihata, M.
collection PubMed
description Cyclin E gene alteration in the cell cycle plays an important role in carcinogenesis, while p53 protein affects different phase checkpoint pathways by activating p21WAF1/CIP1 in the normal cell cycle. We immunohistochemically examined the expression of cyclin E and p53 proteins in 121 patients with transitional cell carcinoma (TCC) of the renal pelvis and ureter to determine their significance for tumour behaviour and patient prognosis. Cyclin E and p53 immunostaining of the nucleus was observed in 36 tumours (29.8%) and 35 tumours (28.9%) respectively. A significant percentage, 69.4% (25 out of 36 tumours), of the cyclin E-positive tumours exhibited simultaneous labelling for p53 (P < 0.05). Mirror-section technique was performed in five selected double-positive tumours to identify cancer cells that were nuclei positive for both cyclin E and p53. The prevalence of cases simultaneously exhibiting both cyclin E and p53 immunostaining was higher in the high-grade tumours (P < 0.01) than in the other types of tumours. Patients with TCCs coexpressing cyclin E and p53 had a significantly poorer prognosis than those expressing neither cyclin E nor p53 (P < 0.001). These in vivo findings provide evidence for cyclin E protein overexpression in TCCs intimately associated with p53 alteration and suggest that simultaneous overexpression of both cyclin E and p53 is related to tumour behaviour and poor prognosis. IMAGES:
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spelling pubmed-21499602009-09-10 Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter. Furihata, M. Ohtsuki, Y. Sonobe, H. Shuin, T. Yamamoto, A. Terao, N. Kuwahara, M. Br J Cancer Research Article Cyclin E gene alteration in the cell cycle plays an important role in carcinogenesis, while p53 protein affects different phase checkpoint pathways by activating p21WAF1/CIP1 in the normal cell cycle. We immunohistochemically examined the expression of cyclin E and p53 proteins in 121 patients with transitional cell carcinoma (TCC) of the renal pelvis and ureter to determine their significance for tumour behaviour and patient prognosis. Cyclin E and p53 immunostaining of the nucleus was observed in 36 tumours (29.8%) and 35 tumours (28.9%) respectively. A significant percentage, 69.4% (25 out of 36 tumours), of the cyclin E-positive tumours exhibited simultaneous labelling for p53 (P < 0.05). Mirror-section technique was performed in five selected double-positive tumours to identify cancer cells that were nuclei positive for both cyclin E and p53. The prevalence of cases simultaneously exhibiting both cyclin E and p53 immunostaining was higher in the high-grade tumours (P < 0.01) than in the other types of tumours. Patients with TCCs coexpressing cyclin E and p53 had a significantly poorer prognosis than those expressing neither cyclin E nor p53 (P < 0.001). These in vivo findings provide evidence for cyclin E protein overexpression in TCCs intimately associated with p53 alteration and suggest that simultaneous overexpression of both cyclin E and p53 is related to tumour behaviour and poor prognosis. IMAGES: Nature Publishing Group 1998-03 /pmc/articles/PMC2149960/ /pubmed/9514058 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
Furihata, M.
Ohtsuki, Y.
Sonobe, H.
Shuin, T.
Yamamoto, A.
Terao, N.
Kuwahara, M.
Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter.
title Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter.
title_full Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter.
title_fullStr Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter.
title_full_unstemmed Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter.
title_short Prognostic significance of cyclin E and p53 protein overexpression in carcinoma of the renal pelvis and ureter.
title_sort prognostic significance of cyclin e and p53 protein overexpression in carcinoma of the renal pelvis and ureter.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2149960/
https://www.ncbi.nlm.nih.gov/pubmed/9514058
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