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HER3 and LINC00052 interplay promotes tumor growth in breast cancer

Here we report that the lncRNA LINC00052 expression correlates positively with HER3/ErbB3 levels in breast cancer cells. Gene silencing of LINC00052 diminished both LINC00052 and HER3 expression and reduced cancer cell growth in vitro and in vivo. LINC00052 overexpression promoted cancer cell growth...

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Autores principales: Salameh, Ahmad, Fan, Xuejun, Choi, Byung-Kwon, Zhang, Shu, Zhang, Ningyan, An, Zhiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351650/
https://www.ncbi.nlm.nih.gov/pubmed/28036286
http://dx.doi.org/10.18632/oncotarget.14313
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author Salameh, Ahmad
Fan, Xuejun
Choi, Byung-Kwon
Zhang, Shu
Zhang, Ningyan
An, Zhiqiang
author_facet Salameh, Ahmad
Fan, Xuejun
Choi, Byung-Kwon
Zhang, Shu
Zhang, Ningyan
An, Zhiqiang
author_sort Salameh, Ahmad
collection PubMed
description Here we report that the lncRNA LINC00052 expression correlates positively with HER3/ErbB3 levels in breast cancer cells. Gene silencing of LINC00052 diminished both LINC00052 and HER3 expression and reduced cancer cell growth in vitro and in vivo. LINC00052 overexpression promoted cancer cell growth in vitro and in vivo and increased HER3-mediated downstream signaling. Importantly, neutralization of HER3 signaling with HER3 targeting monoclonal antibodies blocked LINC00052 mediated cancer cell proliferation in vitro and tumor growth in vivo, suggesting LINC00052 promoting cancer growth through HER3 signaling. Taken together, our results indicate that high LINC00052 levels predict activation of HER3-mediated signaling, and LINC00052 expression level may serve as a potential biomarker for HER3 targeted antibody cancer therapies.
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spelling pubmed-53516502017-04-13 HER3 and LINC00052 interplay promotes tumor growth in breast cancer Salameh, Ahmad Fan, Xuejun Choi, Byung-Kwon Zhang, Shu Zhang, Ningyan An, Zhiqiang Oncotarget Research Paper Here we report that the lncRNA LINC00052 expression correlates positively with HER3/ErbB3 levels in breast cancer cells. Gene silencing of LINC00052 diminished both LINC00052 and HER3 expression and reduced cancer cell growth in vitro and in vivo. LINC00052 overexpression promoted cancer cell growth in vitro and in vivo and increased HER3-mediated downstream signaling. Importantly, neutralization of HER3 signaling with HER3 targeting monoclonal antibodies blocked LINC00052 mediated cancer cell proliferation in vitro and tumor growth in vivo, suggesting LINC00052 promoting cancer growth through HER3 signaling. Taken together, our results indicate that high LINC00052 levels predict activation of HER3-mediated signaling, and LINC00052 expression level may serve as a potential biomarker for HER3 targeted antibody cancer therapies. Impact Journals LLC 2016-12-27 /pmc/articles/PMC5351650/ /pubmed/28036286 http://dx.doi.org/10.18632/oncotarget.14313 Text en Copyright: © 2017 Salameh et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Salameh, Ahmad
Fan, Xuejun
Choi, Byung-Kwon
Zhang, Shu
Zhang, Ningyan
An, Zhiqiang
HER3 and LINC00052 interplay promotes tumor growth in breast cancer
title HER3 and LINC00052 interplay promotes tumor growth in breast cancer
title_full HER3 and LINC00052 interplay promotes tumor growth in breast cancer
title_fullStr HER3 and LINC00052 interplay promotes tumor growth in breast cancer
title_full_unstemmed HER3 and LINC00052 interplay promotes tumor growth in breast cancer
title_short HER3 and LINC00052 interplay promotes tumor growth in breast cancer
title_sort her3 and linc00052 interplay promotes tumor growth in breast cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5351650/
https://www.ncbi.nlm.nih.gov/pubmed/28036286
http://dx.doi.org/10.18632/oncotarget.14313
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