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Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin
BACKGROUND: A promising strategy to overcome the chemoresistance is the tumor blood vessel normalization, which restores the physiological perfusion and oxygenation of tumor vasculature. Thalidomide (Thal) has been shown to increase the anti-tumor effect of chemotherapy agents in solid tumors. Howev...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816178/ https://www.ncbi.nlm.nih.gov/pubmed/31656203 http://dx.doi.org/10.1186/s13046-019-1366-x |
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author | Shen, Yanwei Li, Shuting Wang, Xin Wang, Mengying Tian, Qi Yang, Jiao Wang, Jichang Wang, Biyuan Liu, Peijun Yang, Jin |
author_facet | Shen, Yanwei Li, Shuting Wang, Xin Wang, Mengying Tian, Qi Yang, Jiao Wang, Jichang Wang, Biyuan Liu, Peijun Yang, Jin |
author_sort | Shen, Yanwei |
collection | PubMed |
description | BACKGROUND: A promising strategy to overcome the chemoresistance is the tumor blood vessel normalization, which restores the physiological perfusion and oxygenation of tumor vasculature. Thalidomide (Thal) has been shown to increase the anti-tumor effect of chemotherapy agents in solid tumors. However, it is not yet known whether the synergistic effect of Thal combined with other cytotoxic drugs is attributable to tumor vascular normalization. METHODS: We used two homograft mice models (4 T1 breast tumor model and CT26 colorectal tumor model) to investigate the effect of Thal on tumor growth, microvessel density, vascular physiology, vascular maturity and function, drug delivery and chemosensitivity. Immunofluorescence, immunohistochemistry and scanning electron microscopy were performed to determine the vessel changes. Protein array assay, qPCR and western blotting were used to detect the molecular mechanism by which Thal regulates tumor vascular. RESULTS: Here we report that Thal potently suppressed tumor growth, angiogenesis, hypoxia, and vascular permeability in animal models. Thal also induced a regular monolayer of endothelial cells in tumor vessels, inhibiting vascular instability, and normalized tumor vessels by increasing vascular maturity, pericyte coverage and endothelial junctions. The tumor vessel stabilization effect of Thal resulted in a decrease in tumor vessel tortuosity and leakage, and increased vessel thickness and tumor perfusion. Eventually, the delivery of cisplatin was highly enhanced through the normalized tumor vasculature, thus resulting in profound anti-tumor and anti-metastatic effects. Mechanistically, the effects of Thal on tumor vessels were caused in part by its capability to correct the imbalance between pro-angiogenic factors and anti-angiogenic factors. CONCLUSIONS: Our findings provide direct evidence that Thal remodels the abnormal tumor vessel system into a normalized vasculature. Our results may lay solid foundation for the development of Thal as a novel candidate agent to maximize the therapeutic efficacy of chemotherapeutic drugs for solid tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-019-1366-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6816178 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68161782019-10-31 Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin Shen, Yanwei Li, Shuting Wang, Xin Wang, Mengying Tian, Qi Yang, Jiao Wang, Jichang Wang, Biyuan Liu, Peijun Yang, Jin J Exp Clin Cancer Res Research BACKGROUND: A promising strategy to overcome the chemoresistance is the tumor blood vessel normalization, which restores the physiological perfusion and oxygenation of tumor vasculature. Thalidomide (Thal) has been shown to increase the anti-tumor effect of chemotherapy agents in solid tumors. However, it is not yet known whether the synergistic effect of Thal combined with other cytotoxic drugs is attributable to tumor vascular normalization. METHODS: We used two homograft mice models (4 T1 breast tumor model and CT26 colorectal tumor model) to investigate the effect of Thal on tumor growth, microvessel density, vascular physiology, vascular maturity and function, drug delivery and chemosensitivity. Immunofluorescence, immunohistochemistry and scanning electron microscopy were performed to determine the vessel changes. Protein array assay, qPCR and western blotting were used to detect the molecular mechanism by which Thal regulates tumor vascular. RESULTS: Here we report that Thal potently suppressed tumor growth, angiogenesis, hypoxia, and vascular permeability in animal models. Thal also induced a regular monolayer of endothelial cells in tumor vessels, inhibiting vascular instability, and normalized tumor vessels by increasing vascular maturity, pericyte coverage and endothelial junctions. The tumor vessel stabilization effect of Thal resulted in a decrease in tumor vessel tortuosity and leakage, and increased vessel thickness and tumor perfusion. Eventually, the delivery of cisplatin was highly enhanced through the normalized tumor vasculature, thus resulting in profound anti-tumor and anti-metastatic effects. Mechanistically, the effects of Thal on tumor vessels were caused in part by its capability to correct the imbalance between pro-angiogenic factors and anti-angiogenic factors. CONCLUSIONS: Our findings provide direct evidence that Thal remodels the abnormal tumor vessel system into a normalized vasculature. Our results may lay solid foundation for the development of Thal as a novel candidate agent to maximize the therapeutic efficacy of chemotherapeutic drugs for solid tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-019-1366-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-10-28 /pmc/articles/PMC6816178/ /pubmed/31656203 http://dx.doi.org/10.1186/s13046-019-1366-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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. |
spellingShingle | Research Shen, Yanwei Li, Shuting Wang, Xin Wang, Mengying Tian, Qi Yang, Jiao Wang, Jichang Wang, Biyuan Liu, Peijun Yang, Jin Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin |
title | Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin |
title_full | Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin |
title_fullStr | Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin |
title_full_unstemmed | Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin |
title_short | Tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin |
title_sort | tumor vasculature remolding by thalidomide increases delivery and efficacy of cisplatin |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6816178/ https://www.ncbi.nlm.nih.gov/pubmed/31656203 http://dx.doi.org/10.1186/s13046-019-1366-x |
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