Cargando…

Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts

Insufficient tumor accumulation and distribution of photosensitizers as well as low antitumor immunity severely restrict the therapeutic efficacy of photothermal therapy (PTT). Cancer-associated fibroblasts (CAFs) play a key role in tumor extracellular matrix (ECM) remodeling and immune evasion. Res...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Xin, Yong, Tuying, Wei, Zhaohan, Bie, Nana, Zhang, Xiaoqiong, Zhan, Guiting, Li, Jianye, Qin, Jiaqi, Yu, Jingjing, Zhang, Bixiang, Gan, Lu, Yang, Xiangliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120472/
https://www.ncbi.nlm.nih.gov/pubmed/35589680
http://dx.doi.org/10.1038/s41467-022-30306-7
_version_ 1784710932634533888
author Li, Xin
Yong, Tuying
Wei, Zhaohan
Bie, Nana
Zhang, Xiaoqiong
Zhan, Guiting
Li, Jianye
Qin, Jiaqi
Yu, Jingjing
Zhang, Bixiang
Gan, Lu
Yang, Xiangliang
author_facet Li, Xin
Yong, Tuying
Wei, Zhaohan
Bie, Nana
Zhang, Xiaoqiong
Zhan, Guiting
Li, Jianye
Qin, Jiaqi
Yu, Jingjing
Zhang, Bixiang
Gan, Lu
Yang, Xiangliang
author_sort Li, Xin
collection PubMed
description Insufficient tumor accumulation and distribution of photosensitizers as well as low antitumor immunity severely restrict the therapeutic efficacy of photothermal therapy (PTT). Cancer-associated fibroblasts (CAFs) play a key role in tumor extracellular matrix (ECM) remodeling and immune evasion. Reshaping tumor microenvironment via CAF regulation might provide a potential approach for complete tumor elimination in combination with PTT. Here, tumor cell-derived microparticles co-delivering calcipotriol and Indocyanine green (Cal/ICG@MPs) are developed to modulate CAFs for improved PTT efficacy. Cal/ICG@MPs efficiently target tumor tissues and regulate CAFs to reduce tumor ECM, resulting in enhanced tumor accumulation and penetration of ICG to generate strong PTT efficacy and activate CD8(+) T cell-mediated antitumor immunity. In addition, Cal/ICG@MPs-triggered CAF regulation enhances tumor infiltration of CD8(+) T cells and ameliorates CAF-induced antigen-mediated activation-induced cell death of tumor-specific CD8(+) T cells in response to PTT, eliciting long-term antitumor immune memory to inhibit tumor recurrence and metastasis. Our results support Cal/ICG@MPs as a promising drug to improve PTT efficacy in cancer treatment.
format Online
Article
Text
id pubmed-9120472
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-91204722022-05-21 Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts Li, Xin Yong, Tuying Wei, Zhaohan Bie, Nana Zhang, Xiaoqiong Zhan, Guiting Li, Jianye Qin, Jiaqi Yu, Jingjing Zhang, Bixiang Gan, Lu Yang, Xiangliang Nat Commun Article Insufficient tumor accumulation and distribution of photosensitizers as well as low antitumor immunity severely restrict the therapeutic efficacy of photothermal therapy (PTT). Cancer-associated fibroblasts (CAFs) play a key role in tumor extracellular matrix (ECM) remodeling and immune evasion. Reshaping tumor microenvironment via CAF regulation might provide a potential approach for complete tumor elimination in combination with PTT. Here, tumor cell-derived microparticles co-delivering calcipotriol and Indocyanine green (Cal/ICG@MPs) are developed to modulate CAFs for improved PTT efficacy. Cal/ICG@MPs efficiently target tumor tissues and regulate CAFs to reduce tumor ECM, resulting in enhanced tumor accumulation and penetration of ICG to generate strong PTT efficacy and activate CD8(+) T cell-mediated antitumor immunity. In addition, Cal/ICG@MPs-triggered CAF regulation enhances tumor infiltration of CD8(+) T cells and ameliorates CAF-induced antigen-mediated activation-induced cell death of tumor-specific CD8(+) T cells in response to PTT, eliciting long-term antitumor immune memory to inhibit tumor recurrence and metastasis. Our results support Cal/ICG@MPs as a promising drug to improve PTT efficacy in cancer treatment. Nature Publishing Group UK 2022-05-19 /pmc/articles/PMC9120472/ /pubmed/35589680 http://dx.doi.org/10.1038/s41467-022-30306-7 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
Li, Xin
Yong, Tuying
Wei, Zhaohan
Bie, Nana
Zhang, Xiaoqiong
Zhan, Guiting
Li, Jianye
Qin, Jiaqi
Yu, Jingjing
Zhang, Bixiang
Gan, Lu
Yang, Xiangliang
Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts
title Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts
title_full Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts
title_fullStr Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts
title_full_unstemmed Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts
title_short Reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts
title_sort reversing insufficient photothermal therapy-induced tumor relapse and metastasis by regulating cancer-associated fibroblasts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120472/
https://www.ncbi.nlm.nih.gov/pubmed/35589680
http://dx.doi.org/10.1038/s41467-022-30306-7
work_keys_str_mv AT lixin reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT yongtuying reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT weizhaohan reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT bienana reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT zhangxiaoqiong reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT zhanguiting reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT lijianye reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT qinjiaqi reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT yujingjing reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT zhangbixiang reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT ganlu reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts
AT yangxiangliang reversinginsufficientphotothermaltherapyinducedtumorrelapseandmetastasisbyregulatingcancerassociatedfibroblasts