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The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study

OBJECTIVES: To evaluate p63 expression pattern in Saudi colorectal cancer (CRC) patients and correlate that with clinicopathological parameters and its role in carcinogenesis and prognosis. METHODS: Archival tumor samples were analyzed by immunohistochemistry for p63 expression in 324 consecutive Sa...

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Autores principales: Albasri, Abdulkader M., Elkablawy, Mohammed A., Ansari, Irfan A., Alhujaily, Ahmed S., Khalil, Amal A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535166/
https://www.ncbi.nlm.nih.gov/pubmed/31056618
http://dx.doi.org/10.15537/smj.2019.5.24162
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author Albasri, Abdulkader M.
Elkablawy, Mohammed A.
Ansari, Irfan A.
Alhujaily, Ahmed S.
Khalil, Amal A.
author_facet Albasri, Abdulkader M.
Elkablawy, Mohammed A.
Ansari, Irfan A.
Alhujaily, Ahmed S.
Khalil, Amal A.
author_sort Albasri, Abdulkader M.
collection PubMed
description OBJECTIVES: To evaluate p63 expression pattern in Saudi colorectal cancer (CRC) patients and correlate that with clinicopathological parameters and its role in carcinogenesis and prognosis. METHODS: Archival tumor samples were analyzed by immunohistochemistry for p63 expression in 324 consecutive Saudi patients diagnosed with CRC between January 2006 and December 2017 at the Pathology Department of a tertiary care Hospital, Madinah, Saudi Arabia. RESULTS: P63 over-expression was absent in normal mucosa, while 12.5% cases of adenoma showed its over-expression. In CRC, p63 expression was high in 24.1% of cases. There were no significant correlations between p63 expression and gender, tumor location, tumor size, and tumor histologic differentiation. However, high p63 expression revealed a significant correlation with age (p=0.035), tumor type (p=0.004), American Joint Committee on Cancer stage (p=0.046), lymph node metastasis (p=0.006), lymphovascular invasion (p=0.006), distant metastasis (p=0.049) high Ki67 expression (p=0.000) and K-ras expression (p=0.002). The Kaplan-Meier analysis revealed a shorter period of survival with p63 over-expression (p<0.001). The Cox-regression model analysis showed that p63 over-expression was an independent prognostic marker in CRC (p=0.000). CONCLUSION: P63 expression increased from normal to adenoma to carcinoma sequence. Moreover, p63 cytoplasmic expression seems to be related to high Ki67 indexing, K-ras expression, advanced tumor stage and poor clinical outcome of CRC. These findings suggest a significant role of cytoplasmic p63 expression in tumor progression and prognosis.
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spelling pubmed-65351662019-06-12 The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study Albasri, Abdulkader M. Elkablawy, Mohammed A. Ansari, Irfan A. Alhujaily, Ahmed S. Khalil, Amal A. Saudi Med J Original Article OBJECTIVES: To evaluate p63 expression pattern in Saudi colorectal cancer (CRC) patients and correlate that with clinicopathological parameters and its role in carcinogenesis and prognosis. METHODS: Archival tumor samples were analyzed by immunohistochemistry for p63 expression in 324 consecutive Saudi patients diagnosed with CRC between January 2006 and December 2017 at the Pathology Department of a tertiary care Hospital, Madinah, Saudi Arabia. RESULTS: P63 over-expression was absent in normal mucosa, while 12.5% cases of adenoma showed its over-expression. In CRC, p63 expression was high in 24.1% of cases. There were no significant correlations between p63 expression and gender, tumor location, tumor size, and tumor histologic differentiation. However, high p63 expression revealed a significant correlation with age (p=0.035), tumor type (p=0.004), American Joint Committee on Cancer stage (p=0.046), lymph node metastasis (p=0.006), lymphovascular invasion (p=0.006), distant metastasis (p=0.049) high Ki67 expression (p=0.000) and K-ras expression (p=0.002). The Kaplan-Meier analysis revealed a shorter period of survival with p63 over-expression (p<0.001). The Cox-regression model analysis showed that p63 over-expression was an independent prognostic marker in CRC (p=0.000). CONCLUSION: P63 expression increased from normal to adenoma to carcinoma sequence. Moreover, p63 cytoplasmic expression seems to be related to high Ki67 indexing, K-ras expression, advanced tumor stage and poor clinical outcome of CRC. These findings suggest a significant role of cytoplasmic p63 expression in tumor progression and prognosis. Saudi Medical Journal 2019 /pmc/articles/PMC6535166/ /pubmed/31056618 http://dx.doi.org/10.15537/smj.2019.5.24162 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Albasri, Abdulkader M.
Elkablawy, Mohammed A.
Ansari, Irfan A.
Alhujaily, Ahmed S.
Khalil, Amal A.
The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study
title The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study
title_full The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study
title_fullStr The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study
title_full_unstemmed The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study
title_short The prognostic significance of p63 cytoplasmic expression in colorectal cancer: An immunohistochemical study
title_sort prognostic significance of p63 cytoplasmic expression in colorectal cancer: an immunohistochemical study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535166/
https://www.ncbi.nlm.nih.gov/pubmed/31056618
http://dx.doi.org/10.15537/smj.2019.5.24162
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