Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathway

Abstract In recent years, circular RNA (circRNA) has been found to be involved in a variety of cancer processes. More and more attention has been paid to the research of circRNA in lung cancer. This study aims to investigate whether circ_0000517 affected the physiology of non‐small cell lung cancer...

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Main Authors: Zhong‐Xing Bing, Jia‐Qi Zhang, Gui‐Ge Wang, Yan‐Qing Wang, Tian‐Ge Wang, Dan‐Qing Li
Format: Article
Language:English
Published: Wiley 2021-12-01
Series:Kaohsiung Journal of Medical Sciences
Subjects:
Online Access:https://doi.org/10.1002/kjm2.12440
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author Zhong‐Xing Bing
Jia‐Qi Zhang
Gui‐Ge Wang
Yan‐Qing Wang
Tian‐Ge Wang
Dan‐Qing Li
author_facet Zhong‐Xing Bing
Jia‐Qi Zhang
Gui‐Ge Wang
Yan‐Qing Wang
Tian‐Ge Wang
Dan‐Qing Li
author_sort Zhong‐Xing Bing
collection DOAJ
description Abstract In recent years, circular RNA (circRNA) has been found to be involved in a variety of cancer processes. More and more attention has been paid to the research of circRNA in lung cancer. This study aims to investigate whether circ_0000517 affected the physiology of non‐small cell lung cancer (NSCLC) and the underlying mechanism. The results demonstrated that circ_0000517 was highly expressed in lung cancer tissues and cells, and overexpression of circ_0000517 was negatively correlated with the prognosis of NSCLC patients. Silencing of circ_0000517 significantly inhibited the proliferation, glycolysis, and glutamine decomposition of NSCLC cells in vitro and repressed the growth of xenografted tumors in vivo. Moreover, knockdown of circ_0000517 attenuated the expression of PCNA, HK2, LDHA, ASCT2, and GLS1. Further study found that circ_0000517 targeted miR‐330‐5p and miR‐330‐5p targeted YY1. In addition, miR‐330‐5p inhibitor reversed inhibition of cancer cell proliferation, glycolysis, and glutamine decomposition induced by si‐circ_0000517. In conclusion, our study revealed that silencing of circ_0000517 improved the progression of NSCLC through regulating miR‐330‐5p/YY1 axis.
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spelling doaj.art-a0bc8c2ce55241e0a7679816761c679a2022-12-21T20:39:37ZengWileyKaohsiung Journal of Medical Sciences1607-551X2410-86502021-12-0137121027103710.1002/kjm2.12440Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathwayZhong‐Xing Bing0Jia‐Qi Zhang1Gui‐Ge Wang2Yan‐Qing Wang3Tian‐Ge Wang4Dan‐Qing Li5Department of Thoracic Surgery Peking Union Medical College Hospital Beijing ChinaDepartment of Thoracic Surgery Peking Union Medical College Hospital Beijing ChinaDepartment of Thoracic Surgery Peking Union Medical College Hospital Beijing ChinaDepartment of Thoracic Surgery Peking Union Medical College Hospital Beijing ChinaChinese Academy of Medical Sciences Plastic Surgery Hospital Beijing ChinaDepartment of Thoracic Surgery Peking Union Medical College Hospital Beijing ChinaAbstract In recent years, circular RNA (circRNA) has been found to be involved in a variety of cancer processes. More and more attention has been paid to the research of circRNA in lung cancer. This study aims to investigate whether circ_0000517 affected the physiology of non‐small cell lung cancer (NSCLC) and the underlying mechanism. The results demonstrated that circ_0000517 was highly expressed in lung cancer tissues and cells, and overexpression of circ_0000517 was negatively correlated with the prognosis of NSCLC patients. Silencing of circ_0000517 significantly inhibited the proliferation, glycolysis, and glutamine decomposition of NSCLC cells in vitro and repressed the growth of xenografted tumors in vivo. Moreover, knockdown of circ_0000517 attenuated the expression of PCNA, HK2, LDHA, ASCT2, and GLS1. Further study found that circ_0000517 targeted miR‐330‐5p and miR‐330‐5p targeted YY1. In addition, miR‐330‐5p inhibitor reversed inhibition of cancer cell proliferation, glycolysis, and glutamine decomposition induced by si‐circ_0000517. In conclusion, our study revealed that silencing of circ_0000517 improved the progression of NSCLC through regulating miR‐330‐5p/YY1 axis.https://doi.org/10.1002/kjm2.12440circ_0000517glycolysismiR‐330‐5pNSCLCYY1
spellingShingle Zhong‐Xing Bing
Jia‐Qi Zhang
Gui‐Ge Wang
Yan‐Qing Wang
Tian‐Ge Wang
Dan‐Qing Li
Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathway
Kaohsiung Journal of Medical Sciences
circ_0000517
glycolysis
miR‐330‐5p
NSCLC
YY1
title Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathway
title_full Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathway
title_fullStr Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathway
title_full_unstemmed Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathway
title_short Silencing of circ_0000517 suppresses proliferation, glycolysis, and glutamine decomposition of non‐small cell lung cancer by modulating miR‐330‐5p/YY1 signal pathway
title_sort silencing of circ 0000517 suppresses proliferation glycolysis and glutamine decomposition of non small cell lung cancer by modulating mir 330 5p yy1 signal pathway
topic circ_0000517
glycolysis
miR‐330‐5p
NSCLC
YY1
url https://doi.org/10.1002/kjm2.12440
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