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Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis

The inflammatory factor IL6 secreted by bone marrow mesenchymal stem cells (BMSCs) in the tumor microenvironment (TME) facilitates the survival and therapeutic resistance of neuroblastoma (NB). Here, we found that IL6 expression in primary tumor tissues or bone marrow (BM) metastases was closely ass...

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Autores principales: Zhou, Yang, Yan, Hui, Zhou, Qiang, Feng, Ruiling, Wang, Penggao, Yang, Fang, Zhang, Yaodong, Yuan, Ziqiao, Zhai, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591123/
https://www.ncbi.nlm.nih.gov/pubmed/34790130
http://dx.doi.org/10.3389/fphar.2021.766909
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author Zhou, Yang
Yan, Hui
Zhou, Qiang
Feng, Ruiling
Wang, Penggao
Yang, Fang
Zhang, Yaodong
Yuan, Ziqiao
Zhai, Bo
author_facet Zhou, Yang
Yan, Hui
Zhou, Qiang
Feng, Ruiling
Wang, Penggao
Yang, Fang
Zhang, Yaodong
Yuan, Ziqiao
Zhai, Bo
author_sort Zhou, Yang
collection PubMed
description The inflammatory factor IL6 secreted by bone marrow mesenchymal stem cells (BMSCs) in the tumor microenvironment (TME) facilitates the survival and therapeutic resistance of neuroblastoma (NB). Here, we found that IL6 expression in primary tumor tissues or bone marrow (BM) metastases was closely associated with the disease risk and prognosis of NB patients. IL6 secretion from immortalized BMSC (iBMSC) was directly regulated by NB cells and is involved in promoting the proliferation and metastasis of NB cells. Beta-Lapachone (ARQ-501, LPC), an ortho-naphthoquinone natural product, significantly prevented the iBMSC-induced malignant transformation effect on NB cells through suppressing the expression and secretion of IL6 from iBMSC in vitro and in vivo. Mechanistically, LPC disrupted the crosstalk between NB cells and iBMSC in an NQO1-dependent manner through blocking the Gal-3/Gal-3BP/IL6 axis. Our results reveal the effect of iBMSC-derived IL6 on TME-induced malignant transformation of NB cells, and provide theoretical basis for the clinical application of LPC as a potential IL6 inhibitor in high-risk refractory NB patients.
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spelling pubmed-85911232021-11-16 Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis Zhou, Yang Yan, Hui Zhou, Qiang Feng, Ruiling Wang, Penggao Yang, Fang Zhang, Yaodong Yuan, Ziqiao Zhai, Bo Front Pharmacol Pharmacology The inflammatory factor IL6 secreted by bone marrow mesenchymal stem cells (BMSCs) in the tumor microenvironment (TME) facilitates the survival and therapeutic resistance of neuroblastoma (NB). Here, we found that IL6 expression in primary tumor tissues or bone marrow (BM) metastases was closely associated with the disease risk and prognosis of NB patients. IL6 secretion from immortalized BMSC (iBMSC) was directly regulated by NB cells and is involved in promoting the proliferation and metastasis of NB cells. Beta-Lapachone (ARQ-501, LPC), an ortho-naphthoquinone natural product, significantly prevented the iBMSC-induced malignant transformation effect on NB cells through suppressing the expression and secretion of IL6 from iBMSC in vitro and in vivo. Mechanistically, LPC disrupted the crosstalk between NB cells and iBMSC in an NQO1-dependent manner through blocking the Gal-3/Gal-3BP/IL6 axis. Our results reveal the effect of iBMSC-derived IL6 on TME-induced malignant transformation of NB cells, and provide theoretical basis for the clinical application of LPC as a potential IL6 inhibitor in high-risk refractory NB patients. Frontiers Media S.A. 2021-11-01 /pmc/articles/PMC8591123/ /pubmed/34790130 http://dx.doi.org/10.3389/fphar.2021.766909 Text en Copyright © 2021 Zhou, Yan, Zhou, Feng, Wang, Yang, Zhang, Yuan and Zhai. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Zhou, Yang
Yan, Hui
Zhou, Qiang
Feng, Ruiling
Wang, Penggao
Yang, Fang
Zhang, Yaodong
Yuan, Ziqiao
Zhai, Bo
Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis
title Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis
title_full Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis
title_fullStr Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis
title_full_unstemmed Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis
title_short Beta-Lapachone Attenuates BMSC-Mediated Neuroblastoma Malignant Transformation by Inhibiting Gal-3/Gal-3BP/IL6 Axis
title_sort beta-lapachone attenuates bmsc-mediated neuroblastoma malignant transformation by inhibiting gal-3/gal-3bp/il6 axis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591123/
https://www.ncbi.nlm.nih.gov/pubmed/34790130
http://dx.doi.org/10.3389/fphar.2021.766909
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