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Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells

Ovarian cancer is one of the most lethal gynaecological cancers worldwide. However, the mechanisms underlying ovarian carcinogenesis are not well understood. The present study used immunostaining, western blotting and quantitative real-time PCR to demonstrate that ZNF268 is overexpressed in human ov...

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Autores principales: HU, LI, WANG, WEI, CAI, JINYANG, LUO, JUN, HUANG, YI, XIONG, SHILU, LI, WENXIN, GUO, MINGXIONG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742507/
https://www.ncbi.nlm.nih.gov/pubmed/23946776
http://dx.doi.org/10.3892/ol.2013.1318
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author HU, LI
WANG, WEI
CAI, JINYANG
LUO, JUN
HUANG, YI
XIONG, SHILU
LI, WENXIN
GUO, MINGXIONG
author_facet HU, LI
WANG, WEI
CAI, JINYANG
LUO, JUN
HUANG, YI
XIONG, SHILU
LI, WENXIN
GUO, MINGXIONG
author_sort HU, LI
collection PubMed
description Ovarian cancer is one of the most lethal gynaecological cancers worldwide. However, the mechanisms underlying ovarian carcinogenesis are not well understood. The present study used immunostaining, western blotting and quantitative real-time PCR to demonstrate that ZNF268 is overexpressed in human ovarian carcinomas. ZNF268-knockdown increased the viability, colony formation and growth of in vivo xenografts of ovarian carcinoma SKOV-3 cells, whereas SKOV-3 cell migration was inhibited. Furthermore, it was demonstrated that the knockdown of ZNF268 may increase SKOV-3 cell growth by promoting cell cycle progression. The findings suggest that ZNF268 is a novel protein involved in ovarian carcinogenesis and that it may aid in the understanding of the mechanisms of ovarian carcinogenesis.
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spelling pubmed-37425072013-08-14 Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells HU, LI WANG, WEI CAI, JINYANG LUO, JUN HUANG, YI XIONG, SHILU LI, WENXIN GUO, MINGXIONG Oncol Lett Articles Ovarian cancer is one of the most lethal gynaecological cancers worldwide. However, the mechanisms underlying ovarian carcinogenesis are not well understood. The present study used immunostaining, western blotting and quantitative real-time PCR to demonstrate that ZNF268 is overexpressed in human ovarian carcinomas. ZNF268-knockdown increased the viability, colony formation and growth of in vivo xenografts of ovarian carcinoma SKOV-3 cells, whereas SKOV-3 cell migration was inhibited. Furthermore, it was demonstrated that the knockdown of ZNF268 may increase SKOV-3 cell growth by promoting cell cycle progression. The findings suggest that ZNF268 is a novel protein involved in ovarian carcinogenesis and that it may aid in the understanding of the mechanisms of ovarian carcinogenesis. D.A. Spandidos 2013-07 2013-04-24 /pmc/articles/PMC3742507/ /pubmed/23946776 http://dx.doi.org/10.3892/ol.2013.1318 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
HU, LI
WANG, WEI
CAI, JINYANG
LUO, JUN
HUANG, YI
XIONG, SHILU
LI, WENXIN
GUO, MINGXIONG
Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells
title Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells
title_full Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells
title_fullStr Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells
title_full_unstemmed Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells
title_short Aberrant expression of ZNF268 alters the growth and migration of ovarian cancer cells
title_sort aberrant expression of znf268 alters the growth and migration of ovarian cancer cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3742507/
https://www.ncbi.nlm.nih.gov/pubmed/23946776
http://dx.doi.org/10.3892/ol.2013.1318
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