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IL-22 promotes the progression of breast cancer through regulating HOXB-AS5

Interleukin-22 (IL-22) is a well-known tumor related inflammatory factor that is associated with variety of cancers. HOXB-AS5, a long non-coding RNA located in HOX gene clusters, has been elevated in breast cancer (BC) tissues. Herein, IL-22 and HOXB-AS5 were upregulated in the serum and tissues of...

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Autores principales: Rui, Jiang, Chunming, Zhao, Binbin, Gao, Na, Shao, Shengxi, Wang, Wei, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732753/
https://www.ncbi.nlm.nih.gov/pubmed/29262587
http://dx.doi.org/10.18632/oncotarget.22063
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author Rui, Jiang
Chunming, Zhao
Binbin, Gao
Na, Shao
Shengxi, Wang
Wei, Song
author_facet Rui, Jiang
Chunming, Zhao
Binbin, Gao
Na, Shao
Shengxi, Wang
Wei, Song
author_sort Rui, Jiang
collection PubMed
description Interleukin-22 (IL-22) is a well-known tumor related inflammatory factor that is associated with variety of cancers. HOXB-AS5, a long non-coding RNA located in HOX gene clusters, has been elevated in breast cancer (BC) tissues. Herein, IL-22 and HOXB-AS5 were upregulated in the serum and tissues of BC patients and were associated with clinical stages. Furthermore, we also investigated the effects of IL-22-HOXB-AS5 pathway on progression of BC, and the results suggested that IL-22 and HOXB-AS5 synergistically promoted MDA-MB-231 cell growth, migration and invasion and activated the PI3K-AKT-mTOR pathway. These findings demonstrated that the IL-22-HOXB-AS5-PI3K/AKT functional axes may serve as potential molecule biomarkers for diagnosis and therapy evaluation or targeted therapeutic strategy in BC.
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spelling pubmed-57327532017-12-19 IL-22 promotes the progression of breast cancer through regulating HOXB-AS5 Rui, Jiang Chunming, Zhao Binbin, Gao Na, Shao Shengxi, Wang Wei, Song Oncotarget Research Paper Interleukin-22 (IL-22) is a well-known tumor related inflammatory factor that is associated with variety of cancers. HOXB-AS5, a long non-coding RNA located in HOX gene clusters, has been elevated in breast cancer (BC) tissues. Herein, IL-22 and HOXB-AS5 were upregulated in the serum and tissues of BC patients and were associated with clinical stages. Furthermore, we also investigated the effects of IL-22-HOXB-AS5 pathway on progression of BC, and the results suggested that IL-22 and HOXB-AS5 synergistically promoted MDA-MB-231 cell growth, migration and invasion and activated the PI3K-AKT-mTOR pathway. These findings demonstrated that the IL-22-HOXB-AS5-PI3K/AKT functional axes may serve as potential molecule biomarkers for diagnosis and therapy evaluation or targeted therapeutic strategy in BC. Impact Journals LLC 2017-10-19 /pmc/articles/PMC5732753/ /pubmed/29262587 http://dx.doi.org/10.18632/oncotarget.22063 Text en Copyright: © 2017 Rui 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 (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Rui, Jiang
Chunming, Zhao
Binbin, Gao
Na, Shao
Shengxi, Wang
Wei, Song
IL-22 promotes the progression of breast cancer through regulating HOXB-AS5
title IL-22 promotes the progression of breast cancer through regulating HOXB-AS5
title_full IL-22 promotes the progression of breast cancer through regulating HOXB-AS5
title_fullStr IL-22 promotes the progression of breast cancer through regulating HOXB-AS5
title_full_unstemmed IL-22 promotes the progression of breast cancer through regulating HOXB-AS5
title_short IL-22 promotes the progression of breast cancer through regulating HOXB-AS5
title_sort il-22 promotes the progression of breast cancer through regulating hoxb-as5
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732753/
https://www.ncbi.nlm.nih.gov/pubmed/29262587
http://dx.doi.org/10.18632/oncotarget.22063
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