Cargando…

Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells

Osimertinib is a third‐generation epidermal growth factor receptor tyrosine kinase inhibitor (EGFR‐TKI) for lung adenocarcinoma (LUAD) harboring activating mutations, but patients ultimately develop acquired resistance. Circular RNAs are involved in EGFR‐TKI resistance, while the role of hsa_circ_00...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Suo, Jiang, Zhibin, Xiao, Peng, Li, Xiaozhi, Chen, Yinji, Tang, Hao, Chai, Yanfei, Liu, Yicai, Zhu, Zhao, Xie, Qianyi, He, Wei, Ma, Yuchao, Jin, Longyu, Feng, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748248/
https://www.ncbi.nlm.nih.gov/pubmed/34706132
http://dx.doi.org/10.1111/cas.15177
_version_ 1784630986621845504
author Liu, Suo
Jiang, Zhibin
Xiao, Peng
Li, Xiaozhi
Chen, Yinji
Tang, Hao
Chai, Yanfei
Liu, Yicai
Zhu, Zhao
Xie, Qianyi
He, Wei
Ma, Yuchao
Jin, Longyu
Feng, Wei
author_facet Liu, Suo
Jiang, Zhibin
Xiao, Peng
Li, Xiaozhi
Chen, Yinji
Tang, Hao
Chai, Yanfei
Liu, Yicai
Zhu, Zhao
Xie, Qianyi
He, Wei
Ma, Yuchao
Jin, Longyu
Feng, Wei
author_sort Liu, Suo
collection PubMed
description Osimertinib is a third‐generation epidermal growth factor receptor tyrosine kinase inhibitor (EGFR‐TKI) for lung adenocarcinoma (LUAD) harboring activating mutations, but patients ultimately develop acquired resistance. Circular RNAs are involved in EGFR‐TKI resistance, while the role of hsa_circ_0005576 in the osimertinib resistance of LUAD remains unknown. In this study, we demonstrated that hsa_circ_0005576 could facilitate osimertinib‐resistant LUAD cells. Briefly, knockdown of hsa_circ_0005576 not only suppressed the proliferation and promoted the apoptosis of resistant LUAD cells, but also increased their sensitivity to osimertinib. Mechanistically, hsa_circ_0005576, serving as an miRNA sponge, could directly interact with miR‐512‐5p and subsequently upregulate the miR‐512‐5p‐targeted insulin‐like growth factor 1 receptor. Rescue assays indicated that miR‐512‐5p inhibition could reverse the effects of hsa_circ_0005576 knockdown in LUAD cells resistant to osimertinib. Overall, our study revealed that hsa_circ_0005576 regulates proliferation and apoptosis through miR‐512‐5p/IGF1R signaling, which contributes further to the resistance of LUAD cells to osimertinib. In addition, this study provides a novel insight into the mechanisms underlying osimertinib resistance of LUAD.
format Online
Article
Text
id pubmed-8748248
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-87482482022-01-14 Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells Liu, Suo Jiang, Zhibin Xiao, Peng Li, Xiaozhi Chen, Yinji Tang, Hao Chai, Yanfei Liu, Yicai Zhu, Zhao Xie, Qianyi He, Wei Ma, Yuchao Jin, Longyu Feng, Wei Cancer Sci Original Articles Osimertinib is a third‐generation epidermal growth factor receptor tyrosine kinase inhibitor (EGFR‐TKI) for lung adenocarcinoma (LUAD) harboring activating mutations, but patients ultimately develop acquired resistance. Circular RNAs are involved in EGFR‐TKI resistance, while the role of hsa_circ_0005576 in the osimertinib resistance of LUAD remains unknown. In this study, we demonstrated that hsa_circ_0005576 could facilitate osimertinib‐resistant LUAD cells. Briefly, knockdown of hsa_circ_0005576 not only suppressed the proliferation and promoted the apoptosis of resistant LUAD cells, but also increased their sensitivity to osimertinib. Mechanistically, hsa_circ_0005576, serving as an miRNA sponge, could directly interact with miR‐512‐5p and subsequently upregulate the miR‐512‐5p‐targeted insulin‐like growth factor 1 receptor. Rescue assays indicated that miR‐512‐5p inhibition could reverse the effects of hsa_circ_0005576 knockdown in LUAD cells resistant to osimertinib. Overall, our study revealed that hsa_circ_0005576 regulates proliferation and apoptosis through miR‐512‐5p/IGF1R signaling, which contributes further to the resistance of LUAD cells to osimertinib. In addition, this study provides a novel insight into the mechanisms underlying osimertinib resistance of LUAD. John Wiley and Sons Inc. 2021-11-15 2022-01 /pmc/articles/PMC8748248/ /pubmed/34706132 http://dx.doi.org/10.1111/cas.15177 Text en © 2021 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Liu, Suo
Jiang, Zhibin
Xiao, Peng
Li, Xiaozhi
Chen, Yinji
Tang, Hao
Chai, Yanfei
Liu, Yicai
Zhu, Zhao
Xie, Qianyi
He, Wei
Ma, Yuchao
Jin, Longyu
Feng, Wei
Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells
title Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells
title_full Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells
title_fullStr Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells
title_full_unstemmed Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells
title_short Hsa_circ_0005576 promotes osimertinib resistance through the miR‐512‐5p/IGF1R axis in lung adenocarcinoma cells
title_sort hsa_circ_0005576 promotes osimertinib resistance through the mir‐512‐5p/igf1r axis in lung adenocarcinoma cells
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748248/
https://www.ncbi.nlm.nih.gov/pubmed/34706132
http://dx.doi.org/10.1111/cas.15177
work_keys_str_mv AT liusuo hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT jiangzhibin hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT xiaopeng hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT lixiaozhi hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT chenyinji hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT tanghao hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT chaiyanfei hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT liuyicai hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT zhuzhao hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT xieqianyi hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT hewei hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT mayuchao hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT jinlongyu hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells
AT fengwei hsacirc0005576promotesosimertinibresistancethroughthemir5125pigf1raxisinlungadenocarcinomacells