Cargando…

Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo

PURPOSE: Ovarian cancer is the most lethal malignancy of the female reproductive system, and the prevention and treatment of ovarian carcinoma are still far from optimal. Epidemiological studies reported that ovarian cancer risk was inversely associated with low level of 25-hydroxy vitamin D [25(OH)...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Lizhi, Hu, Zhiyong, Zhang, Hemei, Hou, Yongfeng, Zhang, Zengli, Zhou, Guangming, Li, Bingyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846061/
https://www.ncbi.nlm.nih.gov/pubmed/27143932
http://dx.doi.org/10.2147/OTT.S100581
_version_ 1782429029929844736
author Liu, Lizhi
Hu, Zhiyong
Zhang, Hemei
Hou, Yongfeng
Zhang, Zengli
Zhou, Guangming
Li, Bingyan
author_facet Liu, Lizhi
Hu, Zhiyong
Zhang, Hemei
Hou, Yongfeng
Zhang, Zengli
Zhou, Guangming
Li, Bingyan
author_sort Liu, Lizhi
collection PubMed
description PURPOSE: Ovarian cancer is the most lethal malignancy of the female reproductive system, and the prevention and treatment of ovarian carcinoma are still far from optimal. Epidemiological studies reported that ovarian cancer risk was inversely associated with low level of 25-hydroxy vitamin D [25(OH)]. Therefore, this study focuses on exploring the chemoprevention of vitamin D on epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene (DMBA). METHODS: The mouse ovarian surface epithelial cells were isolated from estrus mice by mild trypsinization and maintained in completed culture medium by repeated passaging. The malignant transformation of mouse ovarian surface epithelial cells was induced by DMBA in vitro. DMBA was directly injected into the bursa of mouse ovary to produce optimized in vivo ovarian cancer model. RESULTS: The results indicate that 1α,25 dihydroxyvitamin D3 may delay malignant transformation of mouse ovarian surface epithelial cells induced by DMBA and significantly decreased the colony formation rate from 18.4% to 3.2% (P<0.05). There was a negative correlation between incidence of DMBA-induced tumor and 25-hydroxy vitamin D level (R(2)=0.978, P<0.05). Vitamin D3 can delay the progression of ovarian cancer induced by DMBA, and the administration of vitamin D3 during the whole process worked more effectively than the administration only during tumor initiation or promotion. Moreover, we found the vitamin D3 increased the expression of E-cadherin and vitamin D receptor while it decreased the expression of β-catenin. CONCLUSION: We succeeded in establishment of epithelial ovarian cancer models both in vitro and in vivo. The DMBA-implanted model in mice yields high incidence and specificity of epithelial derived tumors. We also found that vitamin D delays the progression of ovarian cancer. However, spontaneous epithelial ovarian carcinoma models are still to be explored for testing the preventive effects of vitamin D on epithelial ovarian cancer.
format Online
Article
Text
id pubmed-4846061
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Dove Medical Press
record_format MEDLINE/PubMed
spelling pubmed-48460612016-05-03 Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo Liu, Lizhi Hu, Zhiyong Zhang, Hemei Hou, Yongfeng Zhang, Zengli Zhou, Guangming Li, Bingyan Onco Targets Ther Original Research PURPOSE: Ovarian cancer is the most lethal malignancy of the female reproductive system, and the prevention and treatment of ovarian carcinoma are still far from optimal. Epidemiological studies reported that ovarian cancer risk was inversely associated with low level of 25-hydroxy vitamin D [25(OH)]. Therefore, this study focuses on exploring the chemoprevention of vitamin D on epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene (DMBA). METHODS: The mouse ovarian surface epithelial cells were isolated from estrus mice by mild trypsinization and maintained in completed culture medium by repeated passaging. The malignant transformation of mouse ovarian surface epithelial cells was induced by DMBA in vitro. DMBA was directly injected into the bursa of mouse ovary to produce optimized in vivo ovarian cancer model. RESULTS: The results indicate that 1α,25 dihydroxyvitamin D3 may delay malignant transformation of mouse ovarian surface epithelial cells induced by DMBA and significantly decreased the colony formation rate from 18.4% to 3.2% (P<0.05). There was a negative correlation between incidence of DMBA-induced tumor and 25-hydroxy vitamin D level (R(2)=0.978, P<0.05). Vitamin D3 can delay the progression of ovarian cancer induced by DMBA, and the administration of vitamin D3 during the whole process worked more effectively than the administration only during tumor initiation or promotion. Moreover, we found the vitamin D3 increased the expression of E-cadherin and vitamin D receptor while it decreased the expression of β-catenin. CONCLUSION: We succeeded in establishment of epithelial ovarian cancer models both in vitro and in vivo. The DMBA-implanted model in mice yields high incidence and specificity of epithelial derived tumors. We also found that vitamin D delays the progression of ovarian cancer. However, spontaneous epithelial ovarian carcinoma models are still to be explored for testing the preventive effects of vitamin D on epithelial ovarian cancer. Dove Medical Press 2016-04-19 /pmc/articles/PMC4846061/ /pubmed/27143932 http://dx.doi.org/10.2147/OTT.S100581 Text en © 2016 Liu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Liu, Lizhi
Hu, Zhiyong
Zhang, Hemei
Hou, Yongfeng
Zhang, Zengli
Zhou, Guangming
Li, Bingyan
Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo
title Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo
title_full Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo
title_fullStr Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo
title_full_unstemmed Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo
title_short Vitamin D postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo
title_sort vitamin d postpones the progression of epithelial ovarian cancer induced by 7, 12-dimethylbenz [a] anthracene both in vitro and in vivo
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4846061/
https://www.ncbi.nlm.nih.gov/pubmed/27143932
http://dx.doi.org/10.2147/OTT.S100581
work_keys_str_mv AT liulizhi vitamindpostponestheprogressionofepithelialovariancancerinducedby712dimethylbenzaanthracenebothinvitroandinvivo
AT huzhiyong vitamindpostponestheprogressionofepithelialovariancancerinducedby712dimethylbenzaanthracenebothinvitroandinvivo
AT zhanghemei vitamindpostponestheprogressionofepithelialovariancancerinducedby712dimethylbenzaanthracenebothinvitroandinvivo
AT houyongfeng vitamindpostponestheprogressionofepithelialovariancancerinducedby712dimethylbenzaanthracenebothinvitroandinvivo
AT zhangzengli vitamindpostponestheprogressionofepithelialovariancancerinducedby712dimethylbenzaanthracenebothinvitroandinvivo
AT zhouguangming vitamindpostponestheprogressionofepithelialovariancancerinducedby712dimethylbenzaanthracenebothinvitroandinvivo
AT libingyan vitamindpostponestheprogressionofepithelialovariancancerinducedby712dimethylbenzaanthracenebothinvitroandinvivo