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Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model

The present study evaluated the expression of key molecules and the status of DNA in both oral squamous cell carcinoma (OSCC) and adjacent tissues to establish a molecular surgical boundary and provide a cancer progression model. Biopsy samples from 50 OSCC patients were divided into T (cancer), P1...

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Autores principales: Li, Yi, Li, Bo, Xu, Bo, Han, Bo, Xia, Hui, Chen, Qian-Ming, Li, Long-Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582560/
https://www.ncbi.nlm.nih.gov/pubmed/25835715
http://dx.doi.org/10.1038/ijos.2015.5
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author Li, Yi
Li, Bo
Xu, Bo
Han, Bo
Xia, Hui
Chen, Qian-Ming
Li, Long-Jiang
author_facet Li, Yi
Li, Bo
Xu, Bo
Han, Bo
Xia, Hui
Chen, Qian-Ming
Li, Long-Jiang
author_sort Li, Yi
collection PubMed
description The present study evaluated the expression of key molecules and the status of DNA in both oral squamous cell carcinoma (OSCC) and adjacent tissues to establish a molecular surgical boundary and provide a cancer progression model. Biopsy samples from 50 OSCC patients were divided into T (cancer), P1 (0–0.5 cm), P2 (0.5–1 cm), P3 (1–1.5 cm) and P4 (1.5–2 cm) groups based on the distances from the visible boundary of the primary focus. Twenty samples of normal mucosa were used as controls. We used immunohistochemical staining and flow cytometry to evaluate p53, p21 (CIP1/WAF1) , eIF4E and Ki-67 expression and to determine DNA status, respectively. Sub-mucosal invasion was present in the P1 and P2 groups as determined by haematoxylin and eosin staining. Mutant p53 expression decreased gradually from cancerous to normal mucosae, whereas p21 (CIP1/WAF1) expression displayed an opposite trend. eIF4E expression decreased from cancerous to normal mucosae. Ki-67 expression, the heteroploidy ratio, S-phase fraction and proliferative index decreased gradually with the distance from the tumour centre. Based on these results, we suggest that the resection boundary in OSCC surgery should be beyond 2 cm from the tumour. Additionally, the adjacent tissues of the primary focus could be used as a model for assessing cancer progression.
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spelling pubmed-45825602015-10-06 Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model Li, Yi Li, Bo Xu, Bo Han, Bo Xia, Hui Chen, Qian-Ming Li, Long-Jiang Int J Oral Sci Original Article The present study evaluated the expression of key molecules and the status of DNA in both oral squamous cell carcinoma (OSCC) and adjacent tissues to establish a molecular surgical boundary and provide a cancer progression model. Biopsy samples from 50 OSCC patients were divided into T (cancer), P1 (0–0.5 cm), P2 (0.5–1 cm), P3 (1–1.5 cm) and P4 (1.5–2 cm) groups based on the distances from the visible boundary of the primary focus. Twenty samples of normal mucosa were used as controls. We used immunohistochemical staining and flow cytometry to evaluate p53, p21 (CIP1/WAF1) , eIF4E and Ki-67 expression and to determine DNA status, respectively. Sub-mucosal invasion was present in the P1 and P2 groups as determined by haematoxylin and eosin staining. Mutant p53 expression decreased gradually from cancerous to normal mucosae, whereas p21 (CIP1/WAF1) expression displayed an opposite trend. eIF4E expression decreased from cancerous to normal mucosae. Ki-67 expression, the heteroploidy ratio, S-phase fraction and proliferative index decreased gradually with the distance from the tumour centre. Based on these results, we suggest that the resection boundary in OSCC surgery should be beyond 2 cm from the tumour. Additionally, the adjacent tissues of the primary focus could be used as a model for assessing cancer progression. Nature Publishing Group 2015-09 2015-04-03 /pmc/articles/PMC4582560/ /pubmed/25835715 http://dx.doi.org/10.1038/ijos.2015.5 Text en Copyright © 2015 West China School of Stomatology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Li, Yi
Li, Bo
Xu, Bo
Han, Bo
Xia, Hui
Chen, Qian-Ming
Li, Long-Jiang
Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model
title Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model
title_full Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model
title_fullStr Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model
title_full_unstemmed Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model
title_short Expression of p53, p21 (CIP1/WAF1) and eIF4E in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model
title_sort expression of p53, p21 (cip1/waf1) and eif4e in the adjacent tissues of oral squamous cell carcinoma: establishing the molecular boundary and a cancer progression model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582560/
https://www.ncbi.nlm.nih.gov/pubmed/25835715
http://dx.doi.org/10.1038/ijos.2015.5
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