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p53 Accumulation in Colorectal Cancer with Hepatic Metastasis

The prevalence of immunoreactive p53 and argyrophilic nucleolar organizer region (AgNOR) numbers were compared between colorectal cancers with (n=44) and without (n=51) hepatic metastasis for at least 5 years. At the same time, the distribution of p53‐positive cells in primary, metastatic, and xenog...

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Detalles Bibliográficos
Autores principales: Maruyama, Keiji, Tanaka, Tatsuo, Baba, Shozo, Nakamura, Satoshi, Endo, Yutaka, Sugimura, Haruhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921109/
https://www.ncbi.nlm.nih.gov/pubmed/8641968
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00232.x
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author Maruyama, Keiji
Tanaka, Tatsuo
Baba, Shozo
Nakamura, Satoshi
Endo, Yutaka
Sugimura, Haruhiko
author_facet Maruyama, Keiji
Tanaka, Tatsuo
Baba, Shozo
Nakamura, Satoshi
Endo, Yutaka
Sugimura, Haruhiko
author_sort Maruyama, Keiji
collection PubMed
description The prevalence of immunoreactive p53 and argyrophilic nucleolar organizer region (AgNOR) numbers were compared between colorectal cancers with (n=44) and without (n=51) hepatic metastasis for at least 5 years. At the same time, the distribution of p53‐positive cells in primary, metastatic, and xenografted tumors from the same individuals were studied. Overall, p53 positivity was found more frequently in the cases with hepatic metastasis than in non‐metastatic controls, regardless of the distribution pattern (P<0.05), whereas AgNOR counts were not different between the two groups. Significant heterogeneity in the distribution of p53 immunoreactivity was noted in both the primary and metastatic lesions. The intratumor distribution patterns of p53 immunoreactive cells in the primary (n=33), metastatic (n=33), and xenografted (n=7) tumors of the same individuals were consistent in the majority of cases. There were a few cases in which the p53 immunoreactive cells were more dominant in the metastatic tumor cells. Our observations suggest that p53 accumulation in colorectal cancer is associated with increased risk for hepatic metastasis, while cell proliferation as represented by AgNOR numbers is not. In addition, heterogeneity of abnormal p53 accumulation in the tumor is maintained during the course of metastasis and even after implantation in nude mouse. p53‐Immunoreactive cells in the population of colorectal cancer cells do not necessarily have higher metastasizing potential.
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spelling pubmed-59211092018-05-11 p53 Accumulation in Colorectal Cancer with Hepatic Metastasis Maruyama, Keiji Tanaka, Tatsuo Baba, Shozo Nakamura, Satoshi Endo, Yutaka Sugimura, Haruhiko Jpn J Cancer Res Article The prevalence of immunoreactive p53 and argyrophilic nucleolar organizer region (AgNOR) numbers were compared between colorectal cancers with (n=44) and without (n=51) hepatic metastasis for at least 5 years. At the same time, the distribution of p53‐positive cells in primary, metastatic, and xenografted tumors from the same individuals were studied. Overall, p53 positivity was found more frequently in the cases with hepatic metastasis than in non‐metastatic controls, regardless of the distribution pattern (P<0.05), whereas AgNOR counts were not different between the two groups. Significant heterogeneity in the distribution of p53 immunoreactivity was noted in both the primary and metastatic lesions. The intratumor distribution patterns of p53 immunoreactive cells in the primary (n=33), metastatic (n=33), and xenografted (n=7) tumors of the same individuals were consistent in the majority of cases. There were a few cases in which the p53 immunoreactive cells were more dominant in the metastatic tumor cells. Our observations suggest that p53 accumulation in colorectal cancer is associated with increased risk for hepatic metastasis, while cell proliferation as represented by AgNOR numbers is not. In addition, heterogeneity of abnormal p53 accumulation in the tumor is maintained during the course of metastasis and even after implantation in nude mouse. p53‐Immunoreactive cells in the population of colorectal cancer cells do not necessarily have higher metastasizing potential. Blackwell Publishing Ltd 1996-04 /pmc/articles/PMC5921109/ /pubmed/8641968 http://dx.doi.org/10.1111/j.1349-7006.1996.tb00232.x Text en
spellingShingle Article
Maruyama, Keiji
Tanaka, Tatsuo
Baba, Shozo
Nakamura, Satoshi
Endo, Yutaka
Sugimura, Haruhiko
p53 Accumulation in Colorectal Cancer with Hepatic Metastasis
title p53 Accumulation in Colorectal Cancer with Hepatic Metastasis
title_full p53 Accumulation in Colorectal Cancer with Hepatic Metastasis
title_fullStr p53 Accumulation in Colorectal Cancer with Hepatic Metastasis
title_full_unstemmed p53 Accumulation in Colorectal Cancer with Hepatic Metastasis
title_short p53 Accumulation in Colorectal Cancer with Hepatic Metastasis
title_sort p53 accumulation in colorectal cancer with hepatic metastasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921109/
https://www.ncbi.nlm.nih.gov/pubmed/8641968
http://dx.doi.org/10.1111/j.1349-7006.1996.tb00232.x
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