Several studies demonstrated that angiogenesis is a limiting process for tumour growth and progression. Consequently it is at the same time a potential target for both preventive and therapeutic interventions. Angiogenesis is a multi-step phenomenon that involves different cell types; in particular endothelial cells, tumour cells and immune cells, which orchestrate an intricate network of stimuli aiming to render tumour microenvironment suitable for malignant progression. Here we have demonstrated the anti-angiogenic activity of three compounds derived from naturalling occurring sources: hyperforin (from Saint John’s Wort), methyl-2-cyano-3,12-dioxooleana-1,9-dien-28-oate (CDDO-Me) and 1-[2-cyano-3-,12-dioxooleana-1,9(11)-dien-28-oyl]imidazole (CDDO-Im), both synthetic compounds based on oleanolic acids found in citrus fruits. These compounds could be suitable chemoprevention approaches, and the CDDO derivatives are under study for chemotherapeutic application.

Evaluation of the antiangiogenic and angiopreventive activity of nature-based compounds.

SOGNO, ILARIA
2009

Abstract

Several studies demonstrated that angiogenesis is a limiting process for tumour growth and progression. Consequently it is at the same time a potential target for both preventive and therapeutic interventions. Angiogenesis is a multi-step phenomenon that involves different cell types; in particular endothelial cells, tumour cells and immune cells, which orchestrate an intricate network of stimuli aiming to render tumour microenvironment suitable for malignant progression. Here we have demonstrated the anti-angiogenic activity of three compounds derived from naturalling occurring sources: hyperforin (from Saint John’s Wort), methyl-2-cyano-3,12-dioxooleana-1,9-dien-28-oate (CDDO-Me) and 1-[2-cyano-3-,12-dioxooleana-1,9(11)-dien-28-oyl]imidazole (CDDO-Im), both synthetic compounds based on oleanolic acids found in citrus fruits. These compounds could be suitable chemoprevention approaches, and the CDDO derivatives are under study for chemotherapeutic application.
2009
NOONAN, DOUGLAS
Università degli Studi dell'Insubria
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14242/300857
Il codice NBN di questa tesi è URN:NBN:IT:UNINSUBRIA-300857