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Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis

OBJECTIVE: Glycogen synthase kinase 3β (GSK3β) is a pluripotent protein kinase involved in the development of cancers through regulation of numerous oncogenic molecules. Cyclin D1, an important regulator of G1 to S phase transition in various cells, is one of target proteins that GSK3β regulate. Our...

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Autores principales: Park, Hyunsoo, Lee, Myunghwa, Kim, Dae Woon, Hong, Seo Yoo, Lee, Hojung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Obstetrics and Gynecology; Korean Society of Contraception and Reproductive Health; Korean Society of Gynecologic Endocrinology; Korean Society of Gynecologic Endoscopy and Minimal Invasive Surgery; Korean Society of Maternal Fetal Medicine; Korean Society of Ultrasound in Obstetrics and Gynecology; Korean Urogynecologic Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120066/
https://www.ncbi.nlm.nih.gov/pubmed/27896249
http://dx.doi.org/10.5468/ogs.2016.59.6.470
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author Park, Hyunsoo
Lee, Myunghwa
Kim, Dae Woon
Hong, Seo Yoo
Lee, Hojung
author_facet Park, Hyunsoo
Lee, Myunghwa
Kim, Dae Woon
Hong, Seo Yoo
Lee, Hojung
author_sort Park, Hyunsoo
collection PubMed
description OBJECTIVE: Glycogen synthase kinase 3β (GSK3β) is a pluripotent protein kinase involved in the development of cancers through regulation of numerous oncogenic molecules. Cyclin D1, an important regulator of G1 to S phase transition in various cells, is one of target proteins that GSK3β regulate. Our objective was to assess the expression of GSK3β and cyclin D1 in cervical neoplasm of different histologic grades and to identify their correlation in cervical carcinogenesis. METHODS: Immunohistochemical analysis of GSK3β and cyclin D1 was performed in a total of 137 patients with 12 normal, 62 cervical intraepithelial neoplasia (CIN) (31 CIN1 and 31 CIN3) and 63 invasive cancers including 56 squamous cell carcinomas and 7 adenocarcinomas. RESULTS: The expression of GSK3β increased in parallel with the lesion grade, while that of cyclin D1 decreased with severity of the lesion (P<0.001). There was a significant inverse correlation between GSK3β and cyclin D1 expression in overall cervical neoplasia (Φ=-0.413, P<0.001). GSK3β expression was higher in squamous cell carcinoma than in adenocarcinoma (P=0.049). CONCLUSION: These results suggest that the expressional increase in GSK3β plays a role in cervical carcinogenesis and has inverse correlation with cyclin D1 expression in this process. In addition, GSK3β expression appears to be associated with the histologic type of cervical cancer, especially squamous cell carcinoma.
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spelling pubmed-51200662016-11-28 Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis Park, Hyunsoo Lee, Myunghwa Kim, Dae Woon Hong, Seo Yoo Lee, Hojung Obstet Gynecol Sci Original Article OBJECTIVE: Glycogen synthase kinase 3β (GSK3β) is a pluripotent protein kinase involved in the development of cancers through regulation of numerous oncogenic molecules. Cyclin D1, an important regulator of G1 to S phase transition in various cells, is one of target proteins that GSK3β regulate. Our objective was to assess the expression of GSK3β and cyclin D1 in cervical neoplasm of different histologic grades and to identify their correlation in cervical carcinogenesis. METHODS: Immunohistochemical analysis of GSK3β and cyclin D1 was performed in a total of 137 patients with 12 normal, 62 cervical intraepithelial neoplasia (CIN) (31 CIN1 and 31 CIN3) and 63 invasive cancers including 56 squamous cell carcinomas and 7 adenocarcinomas. RESULTS: The expression of GSK3β increased in parallel with the lesion grade, while that of cyclin D1 decreased with severity of the lesion (P<0.001). There was a significant inverse correlation between GSK3β and cyclin D1 expression in overall cervical neoplasia (Φ=-0.413, P<0.001). GSK3β expression was higher in squamous cell carcinoma than in adenocarcinoma (P=0.049). CONCLUSION: These results suggest that the expressional increase in GSK3β plays a role in cervical carcinogenesis and has inverse correlation with cyclin D1 expression in this process. In addition, GSK3β expression appears to be associated with the histologic type of cervical cancer, especially squamous cell carcinoma. Korean Society of Obstetrics and Gynecology; Korean Society of Contraception and Reproductive Health; Korean Society of Gynecologic Endocrinology; Korean Society of Gynecologic Endoscopy and Minimal Invasive Surgery; Korean Society of Maternal Fetal Medicine; Korean Society of Ultrasound in Obstetrics and Gynecology; Korean Urogynecologic Society 2016-11 2016-11-15 /pmc/articles/PMC5120066/ /pubmed/27896249 http://dx.doi.org/10.5468/ogs.2016.59.6.470 Text en Copyright © 2016 Korean Society of Obstetrics and Gynecology http://creativecommons.org/licenses/by-nc/3.0/ Articles published in Obstet Gynecol Sci are open-access, distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Hyunsoo
Lee, Myunghwa
Kim, Dae Woon
Hong, Seo Yoo
Lee, Hojung
Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis
title Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis
title_full Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis
title_fullStr Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis
title_full_unstemmed Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis
title_short Glycogen synthase kinase 3β and cyclin D1 expression in cervical carcinogenesis
title_sort glycogen synthase kinase 3β and cyclin d1 expression in cervical carcinogenesis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120066/
https://www.ncbi.nlm.nih.gov/pubmed/27896249
http://dx.doi.org/10.5468/ogs.2016.59.6.470
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