Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy

Small-molecule vascular disrupting agents (VDAs) target the established tumor blood vessels, resulting in rapidly and selectively widespread ischemia and necrosis of central tumor; meanwhile, blood flow in normal tissues is relatively unaffected. Although VDAs therapy is considered an important opti...

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Main Authors: Xue-Yuan Wu, Wei Ma, Kiran Gurung, Chi-Hua Guo
Format: Article
Language:English
Published: Elsevier 2013-03-01
Series:Journal of the Formosan Medical Association
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0929664612004743
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spelling doaj-a818171b008f4df3bceec733ee14d6882020-11-24T23:18:58ZengElsevierJournal of the Formosan Medical Association0929-66462013-03-01112311512410.1016/j.jfma.2012.09.017Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapyXue-Yuan WuWei MaKiran GurungChi-Hua GuoSmall-molecule vascular disrupting agents (VDAs) target the established tumor blood vessels, resulting in rapidly and selectively widespread ischemia and necrosis of central tumor; meanwhile, blood flow in normal tissues is relatively unaffected. Although VDAs therapy is considered an important option for treatment, its use is still limited. The tumor cells at the periphery are less sensitive to vascular shutdown than those at the center, and subsequently avoid a nutrient-deprived environment. This phenomenon is referred to as tumor resistance to VDAs treatment. The viable periphery rim of tumor cells contributes to tumor regeneration, metastasis, and ongoing progression. However, there is no systematic review of the plausible mechanisms of repopulation of the viable tumor cells following VDAs therapy. The purpose of this review is to provide insights into mechanisms of tumor surviving small-molecule VDAs therapy, and the synergetic treatment to the remaining viable tumor cells at the periphery.http://www.sciencedirect.com/science/article/pii/S0929664612004743antiangiogenic therapytumor vasculaturevascular disrupting agent
collection DOAJ
language English
format Article
sources DOAJ
author Xue-Yuan Wu
Wei Ma
Kiran Gurung
Chi-Hua Guo
spellingShingle Xue-Yuan Wu
Wei Ma
Kiran Gurung
Chi-Hua Guo
Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy
Journal of the Formosan Medical Association
antiangiogenic therapy
tumor vasculature
vascular disrupting agent
author_facet Xue-Yuan Wu
Wei Ma
Kiran Gurung
Chi-Hua Guo
author_sort Xue-Yuan Wu
title Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy
title_short Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy
title_full Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy
title_fullStr Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy
title_full_unstemmed Mechanisms of tumor resistance to small-molecule vascular disrupting agents: Treatment and rationale of combination therapy
title_sort mechanisms of tumor resistance to small-molecule vascular disrupting agents: treatment and rationale of combination therapy
publisher Elsevier
series Journal of the Formosan Medical Association
issn 0929-6646
publishDate 2013-03-01
description Small-molecule vascular disrupting agents (VDAs) target the established tumor blood vessels, resulting in rapidly and selectively widespread ischemia and necrosis of central tumor; meanwhile, blood flow in normal tissues is relatively unaffected. Although VDAs therapy is considered an important option for treatment, its use is still limited. The tumor cells at the periphery are less sensitive to vascular shutdown than those at the center, and subsequently avoid a nutrient-deprived environment. This phenomenon is referred to as tumor resistance to VDAs treatment. The viable periphery rim of tumor cells contributes to tumor regeneration, metastasis, and ongoing progression. However, there is no systematic review of the plausible mechanisms of repopulation of the viable tumor cells following VDAs therapy. The purpose of this review is to provide insights into mechanisms of tumor surviving small-molecule VDAs therapy, and the synergetic treatment to the remaining viable tumor cells at the periphery.
topic antiangiogenic therapy
tumor vasculature
vascular disrupting agent
url http://www.sciencedirect.com/science/article/pii/S0929664612004743
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