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RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting

The specific biological function of transient receptor potential vanilloid 1 (TRPV1) in pathogenesis of lung adenocarcinoma (LUAD) remains unclear. In this study, TRPV1 expression in tumor tissues, primary cells and cell lines of LUAD, as well as the mechanism mediating its hyperexpression were syst...

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Autores principales: Nie, Yichu, Feng, Fenglan, Luo, Wei, Sanders, Andrew J., Zhang, Yidi, Liang, Jiaming, Chen, Cheng, Feng, Weineng, Gu, Weiquan, Liao, Weiping, Wang, Wei, Chen, Jinfeng, Zhang, Lijian, Jiang, Wen G., Li, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576597/
https://www.ncbi.nlm.nih.gov/pubmed/35354949
http://dx.doi.org/10.1038/s41417-022-00459-0
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author Nie, Yichu
Feng, Fenglan
Luo, Wei
Sanders, Andrew J.
Zhang, Yidi
Liang, Jiaming
Chen, Cheng
Feng, Weineng
Gu, Weiquan
Liao, Weiping
Wang, Wei
Chen, Jinfeng
Zhang, Lijian
Jiang, Wen G.
Li, Jin
author_facet Nie, Yichu
Feng, Fenglan
Luo, Wei
Sanders, Andrew J.
Zhang, Yidi
Liang, Jiaming
Chen, Cheng
Feng, Weineng
Gu, Weiquan
Liao, Weiping
Wang, Wei
Chen, Jinfeng
Zhang, Lijian
Jiang, Wen G.
Li, Jin
author_sort Nie, Yichu
collection PubMed
description The specific biological function of transient receptor potential vanilloid 1 (TRPV1) in pathogenesis of lung adenocarcinoma (LUAD) remains unclear. In this study, TRPV1 expression in tumor tissues, primary cells and cell lines of LUAD, as well as the mechanism mediating its hyperexpression were systematically studied. Multiple models and techniques were adopted to elucidate the relationship between TRPV1 hyperexpression and tumor recurrence and metastasis. Results showed that TRPV1 expression was increased in tumor tissues and primary tumor cells of LUAD patients. The increased expression was associated with worse overall survival outcome and raised HIF1α levels. TRPV1 expression in A549 and NCI-H292 cells was increased after pretreatment with cigarette smoke extract or spermine NONOate. Moreover, A549 cells with TRPV1 overexpression has enhanced tumor growth rates in subcutaneous grafted tumor models, and increased intrapulmonary metastasis after tail vein infusion in nude BALB/c nude mice. Mechanistically, TRPV1 overexpression in A549 cells promoted HIF1α expression and nuclear translocation by promoting CREB phosphorylation and activation of NOS1-NO pathway, ultimately leading to accelerated cell proliferation and stronger invasiveness. In addition, based on photothermal effects, CuS-TRPV1 mAb effectively targeted and induced apoptosis of TRPV1-A549 cells both in vivo and in vitro, thereby mitigating tumor growth and metastasis induced by xenotransplantation of TRPV1-A549 cells. In conclusion, TRPV1 hyperexpression in LUAD is a risk factor for tumor progression and is involved in proliferation and migration of tumor cells through activation of HIF1α. Our study also attempted a new strategy inhibiting the recurrence and metastasis of LUAD: by CuS-TRPV1 mAb precisely kill TRPV1 hyperexpression cells through photothermal effects.
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spelling pubmed-95765972022-10-19 RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting Nie, Yichu Feng, Fenglan Luo, Wei Sanders, Andrew J. Zhang, Yidi Liang, Jiaming Chen, Cheng Feng, Weineng Gu, Weiquan Liao, Weiping Wang, Wei Chen, Jinfeng Zhang, Lijian Jiang, Wen G. Li, Jin Cancer Gene Ther Article The specific biological function of transient receptor potential vanilloid 1 (TRPV1) in pathogenesis of lung adenocarcinoma (LUAD) remains unclear. In this study, TRPV1 expression in tumor tissues, primary cells and cell lines of LUAD, as well as the mechanism mediating its hyperexpression were systematically studied. Multiple models and techniques were adopted to elucidate the relationship between TRPV1 hyperexpression and tumor recurrence and metastasis. Results showed that TRPV1 expression was increased in tumor tissues and primary tumor cells of LUAD patients. The increased expression was associated with worse overall survival outcome and raised HIF1α levels. TRPV1 expression in A549 and NCI-H292 cells was increased after pretreatment with cigarette smoke extract or spermine NONOate. Moreover, A549 cells with TRPV1 overexpression has enhanced tumor growth rates in subcutaneous grafted tumor models, and increased intrapulmonary metastasis after tail vein infusion in nude BALB/c nude mice. Mechanistically, TRPV1 overexpression in A549 cells promoted HIF1α expression and nuclear translocation by promoting CREB phosphorylation and activation of NOS1-NO pathway, ultimately leading to accelerated cell proliferation and stronger invasiveness. In addition, based on photothermal effects, CuS-TRPV1 mAb effectively targeted and induced apoptosis of TRPV1-A549 cells both in vivo and in vitro, thereby mitigating tumor growth and metastasis induced by xenotransplantation of TRPV1-A549 cells. In conclusion, TRPV1 hyperexpression in LUAD is a risk factor for tumor progression and is involved in proliferation and migration of tumor cells through activation of HIF1α. Our study also attempted a new strategy inhibiting the recurrence and metastasis of LUAD: by CuS-TRPV1 mAb precisely kill TRPV1 hyperexpression cells through photothermal effects. Nature Publishing Group US 2022-03-30 2022 /pmc/articles/PMC9576597/ /pubmed/35354949 http://dx.doi.org/10.1038/s41417-022-00459-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nie, Yichu
Feng, Fenglan
Luo, Wei
Sanders, Andrew J.
Zhang, Yidi
Liang, Jiaming
Chen, Cheng
Feng, Weineng
Gu, Weiquan
Liao, Weiping
Wang, Wei
Chen, Jinfeng
Zhang, Lijian
Jiang, Wen G.
Li, Jin
RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting
title RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting
title_full RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting
title_fullStr RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting
title_full_unstemmed RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting
title_short RETRACTED ARTICLE: Overexpressed transient receptor potential vanilloid 1 (TRPV1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting
title_sort retracted article: overexpressed transient receptor potential vanilloid 1 (trpv1) in lung adenocarcinoma harbours a new opportunity for therapeutic targeting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576597/
https://www.ncbi.nlm.nih.gov/pubmed/35354949
http://dx.doi.org/10.1038/s41417-022-00459-0
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