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Understanding the role of CD44V6 in ovarian cancer

This study examined the association of CD44V6 expression in ovarian cancer. We recruited 38 patients with ovarian cancer, 23 with benign ovarian tumor, and 20 with normal ovaries using RT-PCR and western block analysis. Compared with normal ovaries, the expression of CD44V6 mRNA was significantly el...

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Detalles Bibliográficos
Autores principales: Zhang, Hui-Feng, Hu, Peng, Fang, Sheng-Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530090/
https://www.ncbi.nlm.nih.gov/pubmed/28789431
http://dx.doi.org/10.3892/ol.2017.6377
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author Zhang, Hui-Feng
Hu, Peng
Fang, Sheng-Quan
author_facet Zhang, Hui-Feng
Hu, Peng
Fang, Sheng-Quan
author_sort Zhang, Hui-Feng
collection PubMed
description This study examined the association of CD44V6 expression in ovarian cancer. We recruited 38 patients with ovarian cancer, 23 with benign ovarian tumor, and 20 with normal ovaries using RT-PCR and western block analysis. Compared with normal ovaries, the expression of CD44V6 mRNA was significantly elevated in benign ovarian tumor and ovarian cancer. At the protein level, we found no significant differences in CD44V6 expression between normal ovarian tissue and benign ovarian tumor. However, the expression of CD44V6 in ovarian cancer was significantly elevated compared to normal ovaries and benign ovarian tumor. These results were supported by ELISA and western blot analysis. Immunohistochemistry showed that CD44V6 protein in ovarian cancer cells accumulated at high levels on the membrane of ovarian cancer cells. CD44V6 expression is closely associated with the tumorous transformation of ovarian tissue, suggesting that CD44V6 can promote the occurrence and progression of ovarian cancer.
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spelling pubmed-55300902017-08-07 Understanding the role of CD44V6 in ovarian cancer Zhang, Hui-Feng Hu, Peng Fang, Sheng-Quan Oncol Lett Articles This study examined the association of CD44V6 expression in ovarian cancer. We recruited 38 patients with ovarian cancer, 23 with benign ovarian tumor, and 20 with normal ovaries using RT-PCR and western block analysis. Compared with normal ovaries, the expression of CD44V6 mRNA was significantly elevated in benign ovarian tumor and ovarian cancer. At the protein level, we found no significant differences in CD44V6 expression between normal ovarian tissue and benign ovarian tumor. However, the expression of CD44V6 in ovarian cancer was significantly elevated compared to normal ovaries and benign ovarian tumor. These results were supported by ELISA and western blot analysis. Immunohistochemistry showed that CD44V6 protein in ovarian cancer cells accumulated at high levels on the membrane of ovarian cancer cells. CD44V6 expression is closely associated with the tumorous transformation of ovarian tissue, suggesting that CD44V6 can promote the occurrence and progression of ovarian cancer. D.A. Spandidos 2017-08 2017-06-13 /pmc/articles/PMC5530090/ /pubmed/28789431 http://dx.doi.org/10.3892/ol.2017.6377 Text en Copyright: © Zhang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Zhang, Hui-Feng
Hu, Peng
Fang, Sheng-Quan
Understanding the role of CD44V6 in ovarian cancer
title Understanding the role of CD44V6 in ovarian cancer
title_full Understanding the role of CD44V6 in ovarian cancer
title_fullStr Understanding the role of CD44V6 in ovarian cancer
title_full_unstemmed Understanding the role of CD44V6 in ovarian cancer
title_short Understanding the role of CD44V6 in ovarian cancer
title_sort understanding the role of cd44v6 in ovarian cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530090/
https://www.ncbi.nlm.nih.gov/pubmed/28789431
http://dx.doi.org/10.3892/ol.2017.6377
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