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Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer

Cervical cancer is the fourth leading cause of malignancy related mortality in women worldwide. SLC39A7 (ZIP7) is a zinc transporter that plays a key role in intestinal epithelial self-renewal. However, whether or not SLC39A7 is involved in human cervical cancer remains unclear. In this study, we in...

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Detalles Bibliográficos
Autores principales: Wei, Yongqing, Dong, Jie, Li, Fuli, Wei, Zhuqing, Tian, Yuling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735344/
https://www.ncbi.nlm.nih.gov/pubmed/29285013
http://dx.doi.org/10.17179/excli2017-690
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author Wei, Yongqing
Dong, Jie
Li, Fuli
Wei, Zhuqing
Tian, Yuling
author_facet Wei, Yongqing
Dong, Jie
Li, Fuli
Wei, Zhuqing
Tian, Yuling
author_sort Wei, Yongqing
collection PubMed
description Cervical cancer is the fourth leading cause of malignancy related mortality in women worldwide. SLC39A7 (ZIP7) is a zinc transporter that plays a key role in intestinal epithelial self-renewal. However, whether or not SLC39A7 is involved in human cervical cancer remains unclear. In this study, we investigated the effects of SLC39A7 in cervical cancer in vitro and elucidate related underlying mechanisms. Using Oncomine data analysis, we first found SLC39A7 is commonly upregulated in cervical cancer tissues in comparison with corresponding normal controls. The in vitro experiments indicated that silencing of SLC39A7 expression resulted in decreased cell proliferation, increased cell apoptosis, and attenuated migratory and invasive ability using CCK-8, colony formation, flow cytometry, transwell assays, respectively in cervical cancer cell lines, HeLa and ME-180 cells. In molecular levels, Western blot further demonstrated that silencing of SLC39A7 significantly upregulated the expression of Bax and E-cadherin, downregulated the expression of Bcl-2 and MMP-2 in both HeLa and ME-180 cells. These findings provide evidence that SLC39A7 plays a positive role in the progression of cervical cancer and its knockdown might be as a potential therapeutic target for cervical cancer treatment.
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spelling pubmed-57353442017-12-28 Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer Wei, Yongqing Dong, Jie Li, Fuli Wei, Zhuqing Tian, Yuling EXCLI J Original Article Cervical cancer is the fourth leading cause of malignancy related mortality in women worldwide. SLC39A7 (ZIP7) is a zinc transporter that plays a key role in intestinal epithelial self-renewal. However, whether or not SLC39A7 is involved in human cervical cancer remains unclear. In this study, we investigated the effects of SLC39A7 in cervical cancer in vitro and elucidate related underlying mechanisms. Using Oncomine data analysis, we first found SLC39A7 is commonly upregulated in cervical cancer tissues in comparison with corresponding normal controls. The in vitro experiments indicated that silencing of SLC39A7 expression resulted in decreased cell proliferation, increased cell apoptosis, and attenuated migratory and invasive ability using CCK-8, colony formation, flow cytometry, transwell assays, respectively in cervical cancer cell lines, HeLa and ME-180 cells. In molecular levels, Western blot further demonstrated that silencing of SLC39A7 significantly upregulated the expression of Bax and E-cadherin, downregulated the expression of Bcl-2 and MMP-2 in both HeLa and ME-180 cells. These findings provide evidence that SLC39A7 plays a positive role in the progression of cervical cancer and its knockdown might be as a potential therapeutic target for cervical cancer treatment. Leibniz Research Centre for Working Environment and Human Factors 2017-10-24 /pmc/articles/PMC5735344/ /pubmed/29285013 http://dx.doi.org/10.17179/excli2017-690 Text en Copyright © 2017 Wei et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Wei, Yongqing
Dong, Jie
Li, Fuli
Wei, Zhuqing
Tian, Yuling
Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer
title Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer
title_full Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer
title_fullStr Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer
title_full_unstemmed Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer
title_short Knockdown of SLC39A7 suppresses cell proliferation, migration and invasion in cervical cancer
title_sort knockdown of slc39a7 suppresses cell proliferation, migration and invasion in cervical cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735344/
https://www.ncbi.nlm.nih.gov/pubmed/29285013
http://dx.doi.org/10.17179/excli2017-690
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