Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathway

Abstract Little is known about the biological functions of neuron-specific enolase (NSE) as a specific biomarker for small-cell lung cancer (SCLC). Herein, we elucidate the effect and mechanism of NSE on SCLC stem cell-like characteristics. Upregulated NSE expression was observed in spheroid cells....

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Main Authors: Lin Lu, Zhiqiang Zha, Peiling Zhang, Peipei Wang, Xia Liu, Xisheng Fang, Chengyin Weng, Baoxiu Li, Haibo Mao, Lina Wang, Mingmei Guan, Yong Wu, Zhixiang Xu, Zhongqiu Liu, Guolong Liu
Format: Article
Language:English
Published: Nature Publishing Group 2022-04-01
Series:Oncogenesis
Online Access:https://doi.org/10.1038/s41389-022-00396-5
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author Lin Lu
Zhiqiang Zha
Peiling Zhang
Peipei Wang
Xia Liu
Xisheng Fang
Chengyin Weng
Baoxiu Li
Haibo Mao
Lina Wang
Mingmei Guan
Yong Wu
Zhixiang Xu
Zhongqiu Liu
Guolong Liu
author_facet Lin Lu
Zhiqiang Zha
Peiling Zhang
Peipei Wang
Xia Liu
Xisheng Fang
Chengyin Weng
Baoxiu Li
Haibo Mao
Lina Wang
Mingmei Guan
Yong Wu
Zhixiang Xu
Zhongqiu Liu
Guolong Liu
author_sort Lin Lu
collection DOAJ
description Abstract Little is known about the biological functions of neuron-specific enolase (NSE) as a specific biomarker for small-cell lung cancer (SCLC). Herein, we elucidate the effect and mechanism of NSE on SCLC stem cell-like characteristics. Upregulated NSE expression was observed in spheroid cells. The gain-of-function and loss-of-function approaches demonstrated that modulation of NSE positively regulated cell proliferation, drug resistance, spherical clone formation, tumor growth, and stem cell-like characteristics of SCLC cells. Mechanistic studies revealed that NSE might downregulate the expression of neuroblastoma suppressor of tumorigenicity 1 (NBL1) by interacting with NBL1, thereby attenuating the competitive inhibitory effect of NBL1 on BMP2 and enhancing the interaction between BMP2 and BMPR1A; this, in turn, may activate the BMP2/Smad/ID1 pathway and promote SCLC stem cell-like characteristics. Moreover, overexpression of NBL1or knockdown of BMP2 rescued the NSE-induced stem cell-like characteristics. In clinical specimens, NSE expression was positively associated with ALDH1A1 expression and negatively correlated with NBL1 expression. High NSE and ALDH1A1 expressions and low NBL1 expression were correlated with poor prognosis in patients with SCLC. In summary, our study demonstrated that NSE promoted stem cell-like characteristics of SCLC via NBL1 and the activation of the BMP2/Smad/ID1 pathway.
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spelling doaj.art-6c1a21d18fcd4636bd5ea67c9ae045e62022-12-22T03:03:39ZengNature Publishing GroupOncogenesis2157-90242022-04-0111111410.1038/s41389-022-00396-5Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathwayLin Lu0Zhiqiang Zha1Peiling Zhang2Peipei Wang3Xia Liu4Xisheng Fang5Chengyin Weng6Baoxiu Li7Haibo Mao8Lina Wang9Mingmei Guan10Yong Wu11Zhixiang Xu12Zhongqiu Liu13Guolong Liu14Department of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, Guangzhou Medical UniversityDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyDivision of Hematology and Oncology, Comprehensive Cancer Center, the University of Alabama at BirminghamInternational Institute for Translational Chinese Medicine, Guangzhou University of Chinese MedicineDepartment of Medical Oncology, Guangzhou First People’s Hospital, School of Medicine, South China University of TechnologyAbstract Little is known about the biological functions of neuron-specific enolase (NSE) as a specific biomarker for small-cell lung cancer (SCLC). Herein, we elucidate the effect and mechanism of NSE on SCLC stem cell-like characteristics. Upregulated NSE expression was observed in spheroid cells. The gain-of-function and loss-of-function approaches demonstrated that modulation of NSE positively regulated cell proliferation, drug resistance, spherical clone formation, tumor growth, and stem cell-like characteristics of SCLC cells. Mechanistic studies revealed that NSE might downregulate the expression of neuroblastoma suppressor of tumorigenicity 1 (NBL1) by interacting with NBL1, thereby attenuating the competitive inhibitory effect of NBL1 on BMP2 and enhancing the interaction between BMP2 and BMPR1A; this, in turn, may activate the BMP2/Smad/ID1 pathway and promote SCLC stem cell-like characteristics. Moreover, overexpression of NBL1or knockdown of BMP2 rescued the NSE-induced stem cell-like characteristics. In clinical specimens, NSE expression was positively associated with ALDH1A1 expression and negatively correlated with NBL1 expression. High NSE and ALDH1A1 expressions and low NBL1 expression were correlated with poor prognosis in patients with SCLC. In summary, our study demonstrated that NSE promoted stem cell-like characteristics of SCLC via NBL1 and the activation of the BMP2/Smad/ID1 pathway.https://doi.org/10.1038/s41389-022-00396-5
spellingShingle Lin Lu
Zhiqiang Zha
Peiling Zhang
Peipei Wang
Xia Liu
Xisheng Fang
Chengyin Weng
Baoxiu Li
Haibo Mao
Lina Wang
Mingmei Guan
Yong Wu
Zhixiang Xu
Zhongqiu Liu
Guolong Liu
Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathway
Oncogenesis
title Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathway
title_full Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathway
title_fullStr Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathway
title_full_unstemmed Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathway
title_short Neuron-specific enolase promotes stem cell-like characteristics of small-cell lung cancer by downregulating NBL1 and activating the BMP2/Smad/ID1 pathway
title_sort neuron specific enolase promotes stem cell like characteristics of small cell lung cancer by downregulating nbl1 and activating the bmp2 smad id1 pathway
url https://doi.org/10.1038/s41389-022-00396-5
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