Cargando…

Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop

BACKGROUND: Radiation-induced bystander effect (RIBE) can promote tumor metastasis contributing to the failure of radiotherapy for esophageal squamous cell carcinoma (ESCC). Aberrant expression of DJ-1 has been identified in ESCC; however, the relationship between DJ-1 and RIBE in ESCC remains unkno...

Descripción completa

Detalles Bibliográficos
Autores principales: Gu, Junjie, Sun, Yuanyuan, Song, Jiahang, Zhao, Ruiling, Di, Xiaoke, Zhang, Yumeng, Ge, Xiaolin, Zhang, Shu, Gu, Yun, Sun, Xinchen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413943/
https://www.ncbi.nlm.nih.gov/pubmed/36008860
http://dx.doi.org/10.1186/s13046-022-02471-6
_version_ 1784775873522565120
author Gu, Junjie
Sun, Yuanyuan
Song, Jiahang
Zhao, Ruiling
Di, Xiaoke
Zhang, Yumeng
Ge, Xiaolin
Zhang, Shu
Gu, Yun
Sun, Xinchen
author_facet Gu, Junjie
Sun, Yuanyuan
Song, Jiahang
Zhao, Ruiling
Di, Xiaoke
Zhang, Yumeng
Ge, Xiaolin
Zhang, Shu
Gu, Yun
Sun, Xinchen
author_sort Gu, Junjie
collection PubMed
description BACKGROUND: Radiation-induced bystander effect (RIBE) can promote tumor metastasis contributing to the failure of radiotherapy for esophageal squamous cell carcinoma (ESCC). Aberrant expression of DJ-1 has been identified in ESCC; however, the relationship between DJ-1 and RIBE in ESCC remains unknown. METHODS: We detected DJ-1 in the serum and cell supernatants by enzyme-linked immunosorbent assay (ELISA) and evaluated tumor metastasis by phenotypic experiments in vivo and in vitro. RNA-seq, mass spectrometry, western blot (WB), immunoprecipitation (IP), and dual-luciferase reporter assays were performed to explore the underlying mechanisms. RESULTS: DJ-1 was highly expressed in the serum of patients with ESCC receiving radiotherapy and was significantly overexpressed in the medium of ESCC cells receiving irradiation. DJ-1 promoted tumor metastasis via the TGF-β1 pathway. Mechanistic studies revealed that DJ-1 bound to HSC70 to promote Smad3 phosphorylation and nuclear aggregation in a protein-interaction manner, which activated the transcription of Thrombospondin-1 (TSP1). Subsequently, the activation of TGF-β1 by TSP1 re-promoted Smad3 phosphorylation and nuclear aggregation, constituting a positive feedback loop to strengthen the metastasis of ESCC cells, which was effectively blocked by LY2109761 and LSKL. Moreover, higher levels of serum DJ-1 in patients with ESCC were related to a poorer prognosis of radiotherapy. CONCLUSIONS: Irradiation can induce ESCC cells secreting DJ-1. Secreted DJ-1 enters bystander cells to initiate activation of the TGF-β1 pathway via the DJ-1/HSC70/Smad3 signaling axis. The TSP1/TGF-β1/Smad3 positive feedback pathway constitutes the core pathway that promotes ESCC metastasis. DJ-1 is a useful biomarker for predicting the efficacy of radiotherapy and a potential therapeutic target for reversing RIBE in ESCC. GRAPHICAL ABSTRACT: Schematic diagram showing the underlying mechanism that irradiation-induced secretion of DJ-1 accelerates the metastasis of bystander ESCC cells. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-022-02471-6.
format Online
Article
Text
id pubmed-9413943
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-94139432022-08-27 Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop Gu, Junjie Sun, Yuanyuan Song, Jiahang Zhao, Ruiling Di, Xiaoke Zhang, Yumeng Ge, Xiaolin Zhang, Shu Gu, Yun Sun, Xinchen J Exp Clin Cancer Res Research BACKGROUND: Radiation-induced bystander effect (RIBE) can promote tumor metastasis contributing to the failure of radiotherapy for esophageal squamous cell carcinoma (ESCC). Aberrant expression of DJ-1 has been identified in ESCC; however, the relationship between DJ-1 and RIBE in ESCC remains unknown. METHODS: We detected DJ-1 in the serum and cell supernatants by enzyme-linked immunosorbent assay (ELISA) and evaluated tumor metastasis by phenotypic experiments in vivo and in vitro. RNA-seq, mass spectrometry, western blot (WB), immunoprecipitation (IP), and dual-luciferase reporter assays were performed to explore the underlying mechanisms. RESULTS: DJ-1 was highly expressed in the serum of patients with ESCC receiving radiotherapy and was significantly overexpressed in the medium of ESCC cells receiving irradiation. DJ-1 promoted tumor metastasis via the TGF-β1 pathway. Mechanistic studies revealed that DJ-1 bound to HSC70 to promote Smad3 phosphorylation and nuclear aggregation in a protein-interaction manner, which activated the transcription of Thrombospondin-1 (TSP1). Subsequently, the activation of TGF-β1 by TSP1 re-promoted Smad3 phosphorylation and nuclear aggregation, constituting a positive feedback loop to strengthen the metastasis of ESCC cells, which was effectively blocked by LY2109761 and LSKL. Moreover, higher levels of serum DJ-1 in patients with ESCC were related to a poorer prognosis of radiotherapy. CONCLUSIONS: Irradiation can induce ESCC cells secreting DJ-1. Secreted DJ-1 enters bystander cells to initiate activation of the TGF-β1 pathway via the DJ-1/HSC70/Smad3 signaling axis. The TSP1/TGF-β1/Smad3 positive feedback pathway constitutes the core pathway that promotes ESCC metastasis. DJ-1 is a useful biomarker for predicting the efficacy of radiotherapy and a potential therapeutic target for reversing RIBE in ESCC. GRAPHICAL ABSTRACT: Schematic diagram showing the underlying mechanism that irradiation-induced secretion of DJ-1 accelerates the metastasis of bystander ESCC cells. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-022-02471-6. BioMed Central 2022-08-26 /pmc/articles/PMC9413943/ /pubmed/36008860 http://dx.doi.org/10.1186/s13046-022-02471-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Gu, Junjie
Sun, Yuanyuan
Song, Jiahang
Zhao, Ruiling
Di, Xiaoke
Zhang, Yumeng
Ge, Xiaolin
Zhang, Shu
Gu, Yun
Sun, Xinchen
Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop
title Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop
title_full Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop
title_fullStr Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop
title_full_unstemmed Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop
title_short Irradiation induces DJ-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a TGF-β1 positive feedback loop
title_sort irradiation induces dj-1 secretion from esophageal squamous cell carcinoma cells to accelerate metastasis of bystander cells via a tgf-β1 positive feedback loop
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9413943/
https://www.ncbi.nlm.nih.gov/pubmed/36008860
http://dx.doi.org/10.1186/s13046-022-02471-6
work_keys_str_mv AT gujunjie irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT sunyuanyuan irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT songjiahang irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT zhaoruiling irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT dixiaoke irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT zhangyumeng irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT gexiaolin irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT zhangshu irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT guyun irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop
AT sunxinchen irradiationinducesdj1secretionfromesophagealsquamouscellcarcinomacellstoacceleratemetastasisofbystandercellsviaatgfb1positivefeedbackloop