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Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence

Despite the efficacy of current starvation therapies, they are often associated with some intrinsic drawbacks such as poor persistence, facile tumor metastasis and recurrence. Herein, we establish an extravascular gelation shrinkage-derived internal stress strategy for squeezing and narrowing blood...

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Autores principales: Zhang, Kun, Fang, Yan, He, Yaping, Yin, Haohao, Guan, Xin, Pu, Yinying, Zhou, Bangguo, Yue, Wenwen, Ren, Weiwei, Du, Dou, Li, Hongyan, Liu, Chang, Sun, Liping, Chen, Yu, Xu, Huixiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879564/
https://www.ncbi.nlm.nih.gov/pubmed/31772164
http://dx.doi.org/10.1038/s41467-019-13115-3
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author Zhang, Kun
Fang, Yan
He, Yaping
Yin, Haohao
Guan, Xin
Pu, Yinying
Zhou, Bangguo
Yue, Wenwen
Ren, Weiwei
Du, Dou
Li, Hongyan
Liu, Chang
Sun, Liping
Chen, Yu
Xu, Huixiong
author_facet Zhang, Kun
Fang, Yan
He, Yaping
Yin, Haohao
Guan, Xin
Pu, Yinying
Zhou, Bangguo
Yue, Wenwen
Ren, Weiwei
Du, Dou
Li, Hongyan
Liu, Chang
Sun, Liping
Chen, Yu
Xu, Huixiong
author_sort Zhang, Kun
collection PubMed
description Despite the efficacy of current starvation therapies, they are often associated with some intrinsic drawbacks such as poor persistence, facile tumor metastasis and recurrence. Herein, we establish an extravascular gelation shrinkage-derived internal stress strategy for squeezing and narrowing blood vessels, occluding blood & nutrition supply, reducing vascular density, inducing hypoxia and apoptosis and eventually realizing starvation therapy of malignancies. To this end, a biocompatible composite hydrogel consisting of gold nanorods (GNRs) and thermal-sensitive hydrogel mixture was engineered, wherein GRNs can strengthen the structural property of hydrogel mixture and enable robust gelation shrinkage-induced internal stresses. Systematic experiments demonstrate that this starvation therapy can suppress the growths of PANC-1 pancreatic cancer and 4T1 breast cancer. More significantly, this starvation strategy can suppress tumor metastasis and tumor recurrence via reducing vascular density and blood supply and occluding tumor migration passages, which thus provides a promising avenue to comprehensive cancer therapy.
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spelling pubmed-68795642019-11-29 Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence Zhang, Kun Fang, Yan He, Yaping Yin, Haohao Guan, Xin Pu, Yinying Zhou, Bangguo Yue, Wenwen Ren, Weiwei Du, Dou Li, Hongyan Liu, Chang Sun, Liping Chen, Yu Xu, Huixiong Nat Commun Article Despite the efficacy of current starvation therapies, they are often associated with some intrinsic drawbacks such as poor persistence, facile tumor metastasis and recurrence. Herein, we establish an extravascular gelation shrinkage-derived internal stress strategy for squeezing and narrowing blood vessels, occluding blood & nutrition supply, reducing vascular density, inducing hypoxia and apoptosis and eventually realizing starvation therapy of malignancies. To this end, a biocompatible composite hydrogel consisting of gold nanorods (GNRs) and thermal-sensitive hydrogel mixture was engineered, wherein GRNs can strengthen the structural property of hydrogel mixture and enable robust gelation shrinkage-induced internal stresses. Systematic experiments demonstrate that this starvation therapy can suppress the growths of PANC-1 pancreatic cancer and 4T1 breast cancer. More significantly, this starvation strategy can suppress tumor metastasis and tumor recurrence via reducing vascular density and blood supply and occluding tumor migration passages, which thus provides a promising avenue to comprehensive cancer therapy. Nature Publishing Group UK 2019-11-26 /pmc/articles/PMC6879564/ /pubmed/31772164 http://dx.doi.org/10.1038/s41467-019-13115-3 Text en © The Author(s) 2019 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/.
spellingShingle Article
Zhang, Kun
Fang, Yan
He, Yaping
Yin, Haohao
Guan, Xin
Pu, Yinying
Zhou, Bangguo
Yue, Wenwen
Ren, Weiwei
Du, Dou
Li, Hongyan
Liu, Chang
Sun, Liping
Chen, Yu
Xu, Huixiong
Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence
title Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence
title_full Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence
title_fullStr Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence
title_full_unstemmed Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence
title_short Extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence
title_sort extravascular gelation shrinkage-derived internal stress enables tumor starvation therapy with suppressed metastasis and recurrence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6879564/
https://www.ncbi.nlm.nih.gov/pubmed/31772164
http://dx.doi.org/10.1038/s41467-019-13115-3
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