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Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma

Background: Nasopharyngeal carcinoma (NPC) recurrency rate is still high despite patients receiving complete treatment. The response to treatment may vary depending on the type of histopathology and Epstein-Barr virus, however the mechanism remains unclear. Recent studies have found that there is a...

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Autores principales: Yusuf, Muhtarum, Indra, Indriyadevi, Juniati, Sri Herawati, Afriani Dewi, Yussy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581592/
https://www.ncbi.nlm.nih.gov/pubmed/34804499
http://dx.doi.org/10.12688/f1000research.53643.2
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author Yusuf, Muhtarum
Indra, Indriyadevi
Juniati, Sri Herawati
Afriani Dewi, Yussy
author_facet Yusuf, Muhtarum
Indra, Indriyadevi
Juniati, Sri Herawati
Afriani Dewi, Yussy
author_sort Yusuf, Muhtarum
collection PubMed
description Background: Nasopharyngeal carcinoma (NPC) recurrency rate is still high despite patients receiving complete treatment. The response to treatment may vary depending on the type of histopathology and Epstein-Barr virus, however the mechanism remains unclear. Recent studies have found that there is a relationship between response to treatment and the presence of cancer stem cells (CSCs). CD44+ cancer stem cells may cause cancer cells to be resistant to treatment. Therefore, this cross-sectional study aims to determine the correlation between CD44 + cancer stem cell expression and the histopathological types of NPC. Method: Samples were obtained from NPC biopsies of type I, II, III patients (based on WHO histopathology criteria), who had not received prior treatment. CD44+ expression was examined using immunohistochemistry methods by staining CD44+ monoclonal antibodies. The degree of CD44+ cell membrane expression was based on the immunoreactive score scale or the Remmele index scale. Results: Most histopathological types were WHO type III (21 patients, 50%), followed by type II (18 patients, 42.86%), and type I (3 patients, 7.14%). CD44 + expression on type I showed one patient had moderate positive and two patients had a high-positive expression. In type II, 10 were moderate positive and eight were high-positive. In type III, one patient was low-positive, 11 were moderate positive and nine patients were high-positive. Statistical analysis showed that the CD44+ expression difference between the three histopathology types were not statistically significant. Conclusion: There were no correlations between CD44 + expression and histopathological type of NPC.
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spelling pubmed-85815922021-11-18 Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma Yusuf, Muhtarum Indra, Indriyadevi Juniati, Sri Herawati Afriani Dewi, Yussy F1000Res Research Article Background: Nasopharyngeal carcinoma (NPC) recurrency rate is still high despite patients receiving complete treatment. The response to treatment may vary depending on the type of histopathology and Epstein-Barr virus, however the mechanism remains unclear. Recent studies have found that there is a relationship between response to treatment and the presence of cancer stem cells (CSCs). CD44+ cancer stem cells may cause cancer cells to be resistant to treatment. Therefore, this cross-sectional study aims to determine the correlation between CD44 + cancer stem cell expression and the histopathological types of NPC. Method: Samples were obtained from NPC biopsies of type I, II, III patients (based on WHO histopathology criteria), who had not received prior treatment. CD44+ expression was examined using immunohistochemistry methods by staining CD44+ monoclonal antibodies. The degree of CD44+ cell membrane expression was based on the immunoreactive score scale or the Remmele index scale. Results: Most histopathological types were WHO type III (21 patients, 50%), followed by type II (18 patients, 42.86%), and type I (3 patients, 7.14%). CD44 + expression on type I showed one patient had moderate positive and two patients had a high-positive expression. In type II, 10 were moderate positive and eight were high-positive. In type III, one patient was low-positive, 11 were moderate positive and nine patients were high-positive. Statistical analysis showed that the CD44+ expression difference between the three histopathology types were not statistically significant. Conclusion: There were no correlations between CD44 + expression and histopathological type of NPC. F1000 Research Limited 2021-11-03 /pmc/articles/PMC8581592/ /pubmed/34804499 http://dx.doi.org/10.12688/f1000research.53643.2 Text en Copyright: © 2021 Yusuf M et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yusuf, Muhtarum
Indra, Indriyadevi
Juniati, Sri Herawati
Afriani Dewi, Yussy
Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma
title Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma
title_full Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma
title_fullStr Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma
title_full_unstemmed Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma
title_short Correlation between CD44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma
title_sort correlation between cd44+ cancer stem cell expression and histopathological types of nasopharyngeal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8581592/
https://www.ncbi.nlm.nih.gov/pubmed/34804499
http://dx.doi.org/10.12688/f1000research.53643.2
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