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Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma

OBJECTIVE: To measure Lewis y and integrin α(5)β(1) expression in epithelial ovarian carcinoma and to correlate the levels of these molecules with ovarian carcinoma chemotherapy and prognosis. METHODS: The study population included 34 ovarian carcinoma patients with chemotherapeutic drug-resistance,...

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Autores principales: Hu, Zhenhua, Gao, Song, Gao, Jian, Hou, Rui, Liu, Chuan, Liu, Juanjuan, Li, Beibei, Liu, Dawo, Zhang, Shulan, Lin, Bei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546651/
https://www.ncbi.nlm.nih.gov/pubmed/23443083
http://dx.doi.org/10.3390/ijms131215588
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author Hu, Zhenhua
Gao, Song
Gao, Jian
Hou, Rui
Liu, Chuan
Liu, Juanjuan
Li, Beibei
Liu, Dawo
Zhang, Shulan
Lin, Bei
author_facet Hu, Zhenhua
Gao, Song
Gao, Jian
Hou, Rui
Liu, Chuan
Liu, Juanjuan
Li, Beibei
Liu, Dawo
Zhang, Shulan
Lin, Bei
author_sort Hu, Zhenhua
collection PubMed
description OBJECTIVE: To measure Lewis y and integrin α(5)β(1) expression in epithelial ovarian carcinoma and to correlate the levels of these molecules with ovarian carcinoma chemotherapy and prognosis. METHODS: The study population included 34 ovarian carcinoma patients with chemotherapeutic drug-resistance, six partially drug-sensitive cases, and 52 drug-sensitive cases (92 total). Immunochemistry was used to determine expression of Lewis y antigen and integrin α(5)β(1) in ovarian carcinoma tissues, and correlation of these molecules with chemotherapy resistance was further investigated, Multi-factor logistic regression analysis was applied to investigate: age, surgical stage, grade, subtype of patient cases, metastasis of lymph nodes, residual tumor size, expression levels of Lewis y antigen and integrin α(5)β(1) correlation with ovarian carcinoma chemotherapy resistance. RESULTS: The expression rates of Lewis y antigen and integrins α(5) and β(1) were significantly greater in the drug-resistant group (91.17%, 85.29%, 88.24%) than the partially sensitive (50.00%, 33.33%, 50.00%) or sensitive groups (61.54%, 57.69%, 55.77%). Binary logistic regression analysis revealed that surgical stage, residual tumor size, and expression of integrin α(5) and Lewis y in ovarian carcinoma tissues were independent risk factors for chemotherapeutic drug resistance. CONCLUSIONS: Overexpression of Lewis y and integrin α(5) are strong risk factors for chemotherapeutic drug resistance in ovarian carcinoma patients.
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spelling pubmed-35466512013-01-23 Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma Hu, Zhenhua Gao, Song Gao, Jian Hou, Rui Liu, Chuan Liu, Juanjuan Li, Beibei Liu, Dawo Zhang, Shulan Lin, Bei Int J Mol Sci Article OBJECTIVE: To measure Lewis y and integrin α(5)β(1) expression in epithelial ovarian carcinoma and to correlate the levels of these molecules with ovarian carcinoma chemotherapy and prognosis. METHODS: The study population included 34 ovarian carcinoma patients with chemotherapeutic drug-resistance, six partially drug-sensitive cases, and 52 drug-sensitive cases (92 total). Immunochemistry was used to determine expression of Lewis y antigen and integrin α(5)β(1) in ovarian carcinoma tissues, and correlation of these molecules with chemotherapy resistance was further investigated, Multi-factor logistic regression analysis was applied to investigate: age, surgical stage, grade, subtype of patient cases, metastasis of lymph nodes, residual tumor size, expression levels of Lewis y antigen and integrin α(5)β(1) correlation with ovarian carcinoma chemotherapy resistance. RESULTS: The expression rates of Lewis y antigen and integrins α(5) and β(1) were significantly greater in the drug-resistant group (91.17%, 85.29%, 88.24%) than the partially sensitive (50.00%, 33.33%, 50.00%) or sensitive groups (61.54%, 57.69%, 55.77%). Binary logistic regression analysis revealed that surgical stage, residual tumor size, and expression of integrin α(5) and Lewis y in ovarian carcinoma tissues were independent risk factors for chemotherapeutic drug resistance. CONCLUSIONS: Overexpression of Lewis y and integrin α(5) are strong risk factors for chemotherapeutic drug resistance in ovarian carcinoma patients. Molecular Diversity Preservation International (MDPI) 2012-11-23 /pmc/articles/PMC3546651/ /pubmed/23443083 http://dx.doi.org/10.3390/ijms131215588 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Hu, Zhenhua
Gao, Song
Gao, Jian
Hou, Rui
Liu, Chuan
Liu, Juanjuan
Li, Beibei
Liu, Dawo
Zhang, Shulan
Lin, Bei
Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma
title Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma
title_full Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma
title_fullStr Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma
title_full_unstemmed Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma
title_short Elevated Levels of Lewis Y and Integrin α(5)β(1) Correlate with Chemotherapeutic Drug Resistance in Epithelial Ovarian Carcinoma
title_sort elevated levels of lewis y and integrin α(5)β(1) correlate with chemotherapeutic drug resistance in epithelial ovarian carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546651/
https://www.ncbi.nlm.nih.gov/pubmed/23443083
http://dx.doi.org/10.3390/ijms131215588
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