Antiangiogenic and vascular-disrupting agents in endometriosis: pitfalls and promises

Anne Van Langendonckt, Van Langendonckt A, Jacques Donnez, Donnez J, Defrère S, Sylvie Defrère, G.A.J. Dunselman, Dunselman GA, Gerard A J Dunselman, Groothuis PG, Patrick G. Groothuis
Molecular human reproduction · 2008 · vol. 14(5) , pp. 259–268 · doi:10.1093/molehr/gan019 · PMID:18430758 · W2151386917
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This review explores the potential benefits and drawbacks of antiangiogenic and vascular-disrupting agents for treating endometriosis, considering their distinct mechanisms and target disease stages.

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Abstract

It is widely known that angiogenesis plays a key role in endometriotic lesion formation and development. Antiangiogenic treatments aimed at inhibiting new vessel formation have proven efficient in experimental models. However, as antiangiogenic strategies do not target pre-existing pericyte-protected vessels, they require chronic administration and are likely to be beneficial for early-stage disease only or to prevent recurrence after surgery. Moreover, they may have detrimental effects on reproductive function. Vascular-disrupting agents (VDAs) have emerged as a promising new tool for the treatment of tumors. VDAs target established blood vessels, resulting in tumor ischemia and necrosis. These agents may therefore be more efficient against advanced disease. Two major types of VDAs are being developed for cancer: ligand-directed VDAs using antibodies, peptides and growth factors to deliver toxic effectors to tumor endothelium; and small-molecule VDAs exploiting physiological differences between tumor and normal endothelium to induce acute vascular shutdown. The ongoing evolution in genomics and proteomics is revolutionizing the discovery of novel endothelial markers. Several studies suggest that the vasculature of endometriotic lesions may have particular pathophysiological properties, which could be exploited for the development of selective VDAs. The aim of this review is to explore the merits and limitations of vascular therapy for the treatment of endometriosis.

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Condition tags

endometriosis

MeSH descriptors

Angiogenesis Inhibitors Endometriosis Neovascularization, Pathologic Angiogenesis Inhibitors Angiogenesis Inhibitors Angiogenesis Inhibitors Animals Animals Blood Vessels Blood Vessels Blood Vessels Blood Vessels Disease Progression Disease Progression Endometriosis Endometriosis Endometriosis Endometrium Endometrium Endometrium

Citation neighborhood (2-hop)

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (100)

Cited by (50)

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