Prodrug of green tea epigallocatechin-3-gallate (Pro-EGCG) as a potent anti-angiogenesis agent for endometriosis in mice

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A pro-EGCG prodrug significantly inhibited experimental endometriosis in mice by reducing lesion growth, size, and weight, while improving bioavailability and anti-angiogenic capacity compared to EGCG.

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This paper studied whether a prodrug form of green tea epigallocatechin-3-gallate (pro-EGCG, EGCG octaacetate) could inhibit angiogenesis and development of experimental endometriosis in mice. Homologous endometrium was transplanted subcutaneously, and mice received saline, vitamin E, EGCG, or pro-EGCG for 4 weeks, with lesion growth tracked by non-invasive IVIS imaging and angiogenesis assessed by in vivo Cellvizio imaging and SCANCO Microfil microtomography, alongside histology, microvessel, apoptosis, and bioavailability/antioxidation measurements. EGCG and pro-EGCG both significantly reduced lesion growth, size/weight, microvessels, and increased apoptosis by the end of treatment, with pro-EGCG showing greater inhibition across angiogenesis measures and better bioavailability and antioxidant capacity than EGCG; vitamin E had no effect, and ovarian follicles and uterine endometrial glands were not affected. The paper does not explicitly state limitations in the provided text. This paper is centrally about endometriosis — it tests pro-EGCG as an anti-angiogenesis agent to suppress experimental endometriotic lesion growth in mice.

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Abstract

Green tea epigallocatechin-3-gallate (EGCG) can inhibit angiogenesis and development of an experimental endometriosis model in mice, but it suffers from poor bioavailability. A prodrug of EGCG (pro-EGCG, EGCG octaacetate) is utilized to enhance the stability and bioavailability of EGCG in vivo. In this study, the potential of pro-EGCG as a potent anti-angiogenesis agent for endometriosis in mice was investigated. Homologous endometrium was subcutaneously transplanted into mice to receive either saline, vitamin E, EGCG or pro-EGCG treatment for 4 weeks. The growth of the endometrial implants were monitored by IVIS® non-invasive in vivo imaging during the interventions. Angiogenesis of the endometriotic lesions was determined by Cellvizio® in vivo imaging and SCANCO® Microfil microtomography. The bioavailability, anti-oxidation and anti-angiogenesis capacities of the treatments were measured in plasma and lesions. The implants with adjacent outer subcutaneous and inner abdominal muscle layers were collected for histological, microvessel and apoptosis examinations. The result showed that EGCG and pro-EGCG significantly decreased the growth of endometrial implants from the 2nd week to the 4th week of intervention. EGCG and pro-EGCG significantly reduced the lesion size and weight, inhibited functional and structural microvessels in the lesions, and enhanced lesion apoptosis at the end of interventions. The inhibition by pro-EGCG in all the angiogenesis parameters was significantly greater than that by EGCG, and pro-EGCG also had better bioavailability and greater anti-oxidation and anti-angiogenesis capacities than EGCG. Ovarian follicles and uterine endometrial glands were not affected by either EGCG or pro-EGCG. Vitamin E had no effect on endometriosis. In conclusion, pro-EGCG significantly inhibited the development, growth and angiogenesis of experimental endometriosis in mice with high efficacy, bioavailability, anti-oxidation and anti-angiogenesis capacities. Pro-EGCG could be a potent anti-angiogenesis agent for endometriosis. Similar content being viewed by others

References

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Conflict of interest T.H.C. declares that he is the inventor of the issued patent claiming the use of pro-EGCG for proteasome inhibition and the treatment of cancer. The other authors declare there is no conflict of interest. Author information Authors and Affiliations Corresponding author Rights and permissions About this article Cite this article Wang, C.C., Xu, H., Man, G.C.W. et al. Prodrug of green tea epigallocatechin-3-gallate (Pro-EGCG) as a potent anti-angiogenesis agent for endometriosis in mice. Angiogenesis 16, 59–69 (2013). https://doi.org/10.1007/s10456-012-9299-4 Received: Accepted: Published: Issue date: DOI: https://doi.org/10.1007/s10456-012-9299-4

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endometriosis

MeSH descriptors

Angiogenesis Inhibitors Catechin Endometriosis Prodrugs Tea Angiogenesis Inhibitors Angiogenesis Inhibitors Angiogenesis Inhibitors Angiogenesis Inhibitors Animals Apoptosis Apoptosis Biological Availability Catechin Catechin Catechin Catechin Catechin Endometriosis Endometriosis

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