Literature DB >> 9567005

Therapeutic angiogenesis.

J M Isner1, A Takayuki.   

Abstract

Therapeutic angiogenesis constitutes a fundamental survival mechanism that acts to preserve the integrity of tissues subjected to ischemia. Supplemental administration of angiogenic cytokines--as recombinant protein or plasmid DNA--have been shown to augment collateral development when endogenous angiogenesis is suboptimal for organ function, and thus constitute a novel therapeutic option for the treatment of cardiovascular disease. These angiogenic cytokines, all of which share in common the ability to act as mitogens for endothelial cells, do not promote angiogenesis in an indiscriminate fashion; thus angiogenic cytokines selectively produce neovascularization in the ischemic tissues. The purpose of this review is to consider the mechanisms responsible for therapeutic angiogenesis which develops endogenously as well as strategies which have been devised to augment this response. The development of blood vessels is considered from the context of the embryonic paradigm; certain principles which have emerged from studies of pathologic neovascularization; and, principally, the development of collateral blood vessels supplying ischemic tissues, either endogenously or in response to administered growth factors.

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Year:  1998        PMID: 9567005     DOI: 10.2741/a367

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  4 in total

1.  Xiongshao capsule promotes angiogenesis of HUVEC via enhancing cell proliferation and up-regulating the expression of bFGF and VEGF.

Authors:  Jiu-Mao Lin; Jin-Yan Zhao; Qun-Chuan Zhuang; Zhen-Feng Hong; Jun Peng
Journal:  Chin J Integr Med       Date:  2011-11-06       Impact factor: 1.978

Review 2.  [Vascular endothelial factor (VEGF): therapeutic angiogenesis and vasculogenesis in the treatment of cardiovascular disease].

Authors:  C Kalka; T Takahashi; H Masuda; T Asahara; J M Isner
Journal:  Med Klin (Munich)       Date:  1999-04-15

3.  Targeted disruption of the Fgf2 gene does not affect vascular growth in the mouse ischemic hindlimb.

Authors:  Chris J Sullivan; Thomas Doetschman; James B Hoying
Journal:  J Appl Physiol (1985)       Date:  2002-08-16

4.  Osteopontin isoforms differentially promote arteriogenesis in response to ischemia via macrophage accumulation and survival.

Authors:  Grace Sanghee Lee; Hector F Salazar; Giji Joseph; Zoe Shin Yee Lok; Courtney M Caroti; Daiana Weiss; W Robert Taylor; Alicia N Lyle
Journal:  Lab Invest       Date:  2018-06-29       Impact factor: 5.662

  4 in total

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