Harmine inhibits tumour specific neo-vessel formation by regulating VEGF, MMP, TIMP and pro-inflammatory mediators both in vivo and in vitro

Harmine is a beta-carboline alkaloid present in medicinal plants such as Peganum harmala that have been used as folk medicine in anticancer therapy In this study we demonstrated the anti-angiogenic activity of harmine using in vivo and in vitro assay systems In vivo anti angiogenic activity was studied using B16F-10 melanoma cells which induced capillary formation in C57BL/6 mice Intraperitoneal administration of harmine at 10 mg/kg body weight significantly decreased tumour directed capillary formation A drastic elevation in serum pro angiogenic factors such as vascular endothelial growth factor (VEGF) nitric oxide (NO) and pro-inflammatory cytokines in angiogenesis induced animals was significantly decreased by harmine treatment At the same time harmine increased anti-tumour factors like interleukin-2 (IL-2) and tissue inhibitor metalloprotease (TIMP) Moreover nuclear factor (NF)-kappa B and other transcription factors like CREB ATF 2 involved in tumour development and angiogenesis were also inhibited by harmine Various in vitro assays also supported the anti angiogenic activity of harmine It reduced proliferation migration and tube formation of human umbilical vein endothelial cells (HUVEC) Direct treatment of the harmine also inhibited microvessel outgrowth from the rat aortic ring Production of other factors by tumour cells which are involved in angiogenesis like cyclooxygenase (COX-2) inducible nitric oxide synthase (iNOS) and matrix metalloproteases (MMPs) were also decrease by the treatment with harmine Our data suggest that harmine may be a strong angiogenic inhibitor with the ability to decrease the proliferation of vascular endothelial cells and to reduce expression of various pro angiogenic factors (C) 2010 Elsevier B V All rights reserved