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Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family

circNOL10 is a circular RNA expressed at low levels in lung cancer, though its functions in lung cancer remain unknown. Here, the function and molecular mechanism of circNOL10 in lung cancer development are investigated using in vitro and in vivo studies, and it is shown that circNOL10 significantly...

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Autores principales: Nan, Aruo, Chen, Lijian, Zhang, Nan, Jia, Yangyang, Li, Xin, Zhou, Hanyu, Ling, Yihui, Wang, Zhishan, Yang, Chengfeng, Liu, Sijin, Jiang, Yiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343086/
https://www.ncbi.nlm.nih.gov/pubmed/30693177
http://dx.doi.org/10.1002/advs.201800654
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author Nan, Aruo
Chen, Lijian
Zhang, Nan
Jia, Yangyang
Li, Xin
Zhou, Hanyu
Ling, Yihui
Wang, Zhishan
Yang, Chengfeng
Liu, Sijin
Jiang, Yiguo
author_facet Nan, Aruo
Chen, Lijian
Zhang, Nan
Jia, Yangyang
Li, Xin
Zhou, Hanyu
Ling, Yihui
Wang, Zhishan
Yang, Chengfeng
Liu, Sijin
Jiang, Yiguo
author_sort Nan, Aruo
collection PubMed
description circNOL10 is a circular RNA expressed at low levels in lung cancer, though its functions in lung cancer remain unknown. Here, the function and molecular mechanism of circNOL10 in lung cancer development are investigated using in vitro and in vivo studies, and it is shown that circNOL10 significantly inhibits the development of lung cancer and that circNOL10 expression is co‐regulated by methylation of its parental gene Pre‐NOL10 and by splicing factor epithelial splicing regulatory protein 1 (ESRP1). circNOL10 promotes the expression of transcription factor sex comb on midleg‐like 1 (SCML1) by inhibiting transcription factor ubiquitination and thus also affects regulation of the humanin (HN) polypeptide family by SCML1. circNOL10 also affects mitochondrial function through regulating the humanin polypeptide family and affecting multiple signaling pathways, ultimately inhibiting cell proliferation and cell cycle progression, and promoting the apoptosis of lung cancer cells, thereby inhibiting lung cancer development. This study investigates the functions and molecular mechanisms of circNOL10 in the development of lung cancer and reveals its involvement in the transcriptional regulation of the HN polypeptide family by SCML1. The results also demonstrate the inhibitory effect of HN on lung cancer cells growth. These findings may identify novel targets for the molecular therapy of lung cancer.
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spelling pubmed-63430862019-01-28 Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family Nan, Aruo Chen, Lijian Zhang, Nan Jia, Yangyang Li, Xin Zhou, Hanyu Ling, Yihui Wang, Zhishan Yang, Chengfeng Liu, Sijin Jiang, Yiguo Adv Sci (Weinh) Full Papers circNOL10 is a circular RNA expressed at low levels in lung cancer, though its functions in lung cancer remain unknown. Here, the function and molecular mechanism of circNOL10 in lung cancer development are investigated using in vitro and in vivo studies, and it is shown that circNOL10 significantly inhibits the development of lung cancer and that circNOL10 expression is co‐regulated by methylation of its parental gene Pre‐NOL10 and by splicing factor epithelial splicing regulatory protein 1 (ESRP1). circNOL10 promotes the expression of transcription factor sex comb on midleg‐like 1 (SCML1) by inhibiting transcription factor ubiquitination and thus also affects regulation of the humanin (HN) polypeptide family by SCML1. circNOL10 also affects mitochondrial function through regulating the humanin polypeptide family and affecting multiple signaling pathways, ultimately inhibiting cell proliferation and cell cycle progression, and promoting the apoptosis of lung cancer cells, thereby inhibiting lung cancer development. This study investigates the functions and molecular mechanisms of circNOL10 in the development of lung cancer and reveals its involvement in the transcriptional regulation of the HN polypeptide family by SCML1. The results also demonstrate the inhibitory effect of HN on lung cancer cells growth. These findings may identify novel targets for the molecular therapy of lung cancer. John Wiley and Sons Inc. 2018-11-16 /pmc/articles/PMC6343086/ /pubmed/30693177 http://dx.doi.org/10.1002/advs.201800654 Text en © 2018 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Nan, Aruo
Chen, Lijian
Zhang, Nan
Jia, Yangyang
Li, Xin
Zhou, Hanyu
Ling, Yihui
Wang, Zhishan
Yang, Chengfeng
Liu, Sijin
Jiang, Yiguo
Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family
title Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family
title_full Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family
title_fullStr Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family
title_full_unstemmed Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family
title_short Circular RNA circNOL10 Inhibits Lung Cancer Development by Promoting SCLM1‐Mediated Transcriptional Regulation of the Humanin Polypeptide Family
title_sort circular rna circnol10 inhibits lung cancer development by promoting sclm1‐mediated transcriptional regulation of the humanin polypeptide family
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6343086/
https://www.ncbi.nlm.nih.gov/pubmed/30693177
http://dx.doi.org/10.1002/advs.201800654
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