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Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy

LncRNA plays a crucial role in human disease. However, the expression and function of LncRNA in ICP(Intrahepatic cholestasis of pregnancy) is still not fully elucidated. In this study, we found Linc02527 was increased expression in placenta and serum of ICP patients. Ectopically expression of Linc02...

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Autores principales: Hu, Jianguo, Liu, Li, Gong, Yangyang, Zhang, Lei, Gan, Xiaoling, Luo, Xiaodong, Yu, Tinghe, Zhong, Xiaocui, Deng, Xinru, Hu, Lina, Zhang, Zhanyu, Dong, Xiaojing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155230/
https://www.ncbi.nlm.nih.gov/pubmed/30250023
http://dx.doi.org/10.1038/s41419-018-1013-z
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author Hu, Jianguo
Liu, Li
Gong, Yangyang
Zhang, Lei
Gan, Xiaoling
Luo, Xiaodong
Yu, Tinghe
Zhong, Xiaocui
Deng, Xinru
Hu, Lina
Zhang, Zhanyu
Dong, Xiaojing
author_facet Hu, Jianguo
Liu, Li
Gong, Yangyang
Zhang, Lei
Gan, Xiaoling
Luo, Xiaodong
Yu, Tinghe
Zhong, Xiaocui
Deng, Xinru
Hu, Lina
Zhang, Zhanyu
Dong, Xiaojing
author_sort Hu, Jianguo
collection PubMed
description LncRNA plays a crucial role in human disease. However, the expression and function of LncRNA in ICP(Intrahepatic cholestasis of pregnancy) is still not fully elucidated. In this study, we found Linc02527 was increased expression in placenta and serum of ICP patients. Ectopically expression of Linc02527 promoted autophagy and proliferate in HTR8 cells. Silencing Linc02527 suppressed the autophagy and proliferate in HTR8 cells. Mechanically study revealed that Linc02527 regulated the expression of ATG5 and ATG7 by sponging miR-3185. Linc02527 directly binding to YBX1 and activated P21. The growth of C57 mouse was retarded when autophagy was activated. In normal condition, inhibited autophagy using chloroquine did not affect the growth of C57 mouse. However, in the condition of autophagy was activated, inhibited autophagy using chloroquine can improve the growth of C57 mouse. Overall, the results of this study identified Linc02527 as a candidate biomarker in ICP and a potential target for ICP therapy. Chloroquine was a potential drug for ICP therapy.
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spelling pubmed-61552302018-09-28 Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy Hu, Jianguo Liu, Li Gong, Yangyang Zhang, Lei Gan, Xiaoling Luo, Xiaodong Yu, Tinghe Zhong, Xiaocui Deng, Xinru Hu, Lina Zhang, Zhanyu Dong, Xiaojing Cell Death Dis Article LncRNA plays a crucial role in human disease. However, the expression and function of LncRNA in ICP(Intrahepatic cholestasis of pregnancy) is still not fully elucidated. In this study, we found Linc02527 was increased expression in placenta and serum of ICP patients. Ectopically expression of Linc02527 promoted autophagy and proliferate in HTR8 cells. Silencing Linc02527 suppressed the autophagy and proliferate in HTR8 cells. Mechanically study revealed that Linc02527 regulated the expression of ATG5 and ATG7 by sponging miR-3185. Linc02527 directly binding to YBX1 and activated P21. The growth of C57 mouse was retarded when autophagy was activated. In normal condition, inhibited autophagy using chloroquine did not affect the growth of C57 mouse. However, in the condition of autophagy was activated, inhibited autophagy using chloroquine can improve the growth of C57 mouse. Overall, the results of this study identified Linc02527 as a candidate biomarker in ICP and a potential target for ICP therapy. Chloroquine was a potential drug for ICP therapy. Nature Publishing Group UK 2018-09-24 /pmc/articles/PMC6155230/ /pubmed/30250023 http://dx.doi.org/10.1038/s41419-018-1013-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hu, Jianguo
Liu, Li
Gong, Yangyang
Zhang, Lei
Gan, Xiaoling
Luo, Xiaodong
Yu, Tinghe
Zhong, Xiaocui
Deng, Xinru
Hu, Lina
Zhang, Zhanyu
Dong, Xiaojing
Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy
title Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy
title_full Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy
title_fullStr Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy
title_full_unstemmed Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy
title_short Linc02527 promoted autophagy in Intrahepatic cholestasis of pregnancy
title_sort linc02527 promoted autophagy in intrahepatic cholestasis of pregnancy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155230/
https://www.ncbi.nlm.nih.gov/pubmed/30250023
http://dx.doi.org/10.1038/s41419-018-1013-z
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