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TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer
BACKGROUND: Recent developments in abscopal effect strongly support the use of radiotherapy for the treatment of metastatic disease. However, deeper understanding of the molecular mechanisms underlying the abscopal effect are required to best benefit a larger proportion of patients with metastasis....
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934399/ https://www.ncbi.nlm.nih.gov/pubmed/33673859 http://dx.doi.org/10.1186/s13046-021-01883-0 |
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author | Tesei, Anna Arienti, Chiara Bossi, Gianluca Santi, Spartaco De Santis, Ilaria Bevilacqua, Alessandro Zanoni, Michele Pignatta, Sara Cortesi, Michela Zamagni, Alice Storci, Gianluca Bonafè, Massimiliano Sarnelli, Anna Romeo, Antonino Cavallo, Carola Bartolazzi, Armando Rossi, Stefania Soriani, Antonella Strigari, Lidia |
author_facet | Tesei, Anna Arienti, Chiara Bossi, Gianluca Santi, Spartaco De Santis, Ilaria Bevilacqua, Alessandro Zanoni, Michele Pignatta, Sara Cortesi, Michela Zamagni, Alice Storci, Gianluca Bonafè, Massimiliano Sarnelli, Anna Romeo, Antonino Cavallo, Carola Bartolazzi, Armando Rossi, Stefania Soriani, Antonella Strigari, Lidia |
author_sort | Tesei, Anna |
collection | PubMed |
description | BACKGROUND: Recent developments in abscopal effect strongly support the use of radiotherapy for the treatment of metastatic disease. However, deeper understanding of the molecular mechanisms underlying the abscopal effect are required to best benefit a larger proportion of patients with metastasis. Several groups including ours, reported the involvement of wild-type (wt) p53 in radiation-induced abscopal effects, however very little is known on the role of wtp53 dependent molecular mechanisms. METHODS: We investigated through in vivo and in vitro approaches how wtp53 orchestrates radiation-induced abscopal effects. Wtp53 bearing (A549) and p53-null (H1299) NSCLC lines were xenotransplanted in nude mice, and cultured in 2D monolayers and 3D tumor spheroids. Extracellular vesicles (EVs) were isolated from medium cell culture by ultracentrifugation protocol followed by Nanoparticle Tracking Analysis. Gene expression was evaluated by RT-Real Time, digital qRT-PCR, and dot blot technique. Protein levels were determined by immunohistochemistry, confocal anlysis, western blot techniques, and immunoassay. RESULTS: We demonstrated that single high-dose irradiation (20 Gy) induces significant tumor growth inhibition in contralateral non-irradiated (NIR) A549 xenograft tumors but not in NIR p53-null H1299 or p53-silenced A549 (A549sh/p53) xenografts. We further demonstrates that irradiation of A549 cells in vitro induces a senescence-associated secretory phenotype (SASP) producing extracellular vesicles (EVs) expressing CD63 and carrying DNA:RNA hybrids and LINE-1 retrotransposon. IR-A549 EVs also hamper the colony-forming capability of recipient NIR A549 cells, induce senescent phenotype, nuclear expression of DNA:RNA hybrids, and M1 macrophage polarization. CONCLUSIONS: In our models, we demonstrate that high radiation dose in wtp53 tumors induce the onset of SASP and secretion of CD63+ EVs loaded with DNA:RNA hybrids and LINE-1 retrotransposons that convey senescence messages out of the irradiation field triggering abscopal effect in NIR tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-021-01883-0. |
format | Online Article Text |
id | pubmed-7934399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79343992021-03-08 TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer Tesei, Anna Arienti, Chiara Bossi, Gianluca Santi, Spartaco De Santis, Ilaria Bevilacqua, Alessandro Zanoni, Michele Pignatta, Sara Cortesi, Michela Zamagni, Alice Storci, Gianluca Bonafè, Massimiliano Sarnelli, Anna Romeo, Antonino Cavallo, Carola Bartolazzi, Armando Rossi, Stefania Soriani, Antonella Strigari, Lidia J Exp Clin Cancer Res Research BACKGROUND: Recent developments in abscopal effect strongly support the use of radiotherapy for the treatment of metastatic disease. However, deeper understanding of the molecular mechanisms underlying the abscopal effect are required to best benefit a larger proportion of patients with metastasis. Several groups including ours, reported the involvement of wild-type (wt) p53 in radiation-induced abscopal effects, however very little is known on the role of wtp53 dependent molecular mechanisms. METHODS: We investigated through in vivo and in vitro approaches how wtp53 orchestrates radiation-induced abscopal effects. Wtp53 bearing (A549) and p53-null (H1299) NSCLC lines were xenotransplanted in nude mice, and cultured in 2D monolayers and 3D tumor spheroids. Extracellular vesicles (EVs) were isolated from medium cell culture by ultracentrifugation protocol followed by Nanoparticle Tracking Analysis. Gene expression was evaluated by RT-Real Time, digital qRT-PCR, and dot blot technique. Protein levels were determined by immunohistochemistry, confocal anlysis, western blot techniques, and immunoassay. RESULTS: We demonstrated that single high-dose irradiation (20 Gy) induces significant tumor growth inhibition in contralateral non-irradiated (NIR) A549 xenograft tumors but not in NIR p53-null H1299 or p53-silenced A549 (A549sh/p53) xenografts. We further demonstrates that irradiation of A549 cells in vitro induces a senescence-associated secretory phenotype (SASP) producing extracellular vesicles (EVs) expressing CD63 and carrying DNA:RNA hybrids and LINE-1 retrotransposon. IR-A549 EVs also hamper the colony-forming capability of recipient NIR A549 cells, induce senescent phenotype, nuclear expression of DNA:RNA hybrids, and M1 macrophage polarization. CONCLUSIONS: In our models, we demonstrate that high radiation dose in wtp53 tumors induce the onset of SASP and secretion of CD63+ EVs loaded with DNA:RNA hybrids and LINE-1 retrotransposons that convey senescence messages out of the irradiation field triggering abscopal effect in NIR tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-021-01883-0. BioMed Central 2021-03-05 /pmc/articles/PMC7934399/ /pubmed/33673859 http://dx.doi.org/10.1186/s13046-021-01883-0 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Tesei, Anna Arienti, Chiara Bossi, Gianluca Santi, Spartaco De Santis, Ilaria Bevilacqua, Alessandro Zanoni, Michele Pignatta, Sara Cortesi, Michela Zamagni, Alice Storci, Gianluca Bonafè, Massimiliano Sarnelli, Anna Romeo, Antonino Cavallo, Carola Bartolazzi, Armando Rossi, Stefania Soriani, Antonella Strigari, Lidia TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer |
title | TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer |
title_full | TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer |
title_fullStr | TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer |
title_full_unstemmed | TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer |
title_short | TP53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer |
title_sort | tp53 drives abscopal effect by secretion of senescence-associated molecular signals in non-small cell lung cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934399/ https://www.ncbi.nlm.nih.gov/pubmed/33673859 http://dx.doi.org/10.1186/s13046-021-01883-0 |
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