The Past and Future of Angiogenesis as a Target for Cancer Therapy and Prevention

Author:

Albini Adriana1ORCID,Noonan Douglas M.23ORCID,Corradino Paola1ORCID,Magnoni Francesca1ORCID,Corso Giovanni14ORCID

Affiliation:

1. European Institute of Oncologi IEO, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Milan, Italy. 1

2. Department of Biotechnology and Life Sciences, University of Insubria, Varese, Italy. 2

3. IRCCS MultiMedica, Milan, Italy. 3

4. Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy. 4

Abstract

Abstract Cancer growth is dependent on angiogenesis, the formation of new blood vessels, which represents a hallmark of cancer. After this concept was established in the 1970s, inhibition of tumor development and metastases by blocking the neoangiogenic process has been an important approach to the treatment of tumors. However, antiangiogenic therapies are often administered when cancer has already progressed. The key to reducing the cancer burden is prevention. We noticed 20 years ago that a series of possible cancer chemopreventive agents showed antiangiogenic properties when tested in experimental models. This article reviews the relevant advances in the understanding of the rationale for targeting angiogenesis for cancer therapy, prevention, and interception and recently investigated substances with antiangiogenic activity that may be suitable for such strategies. Many compounds, either dietary derivatives or repurposed drugs, with antiangiogenic activity are possible tools for cancer angioprevention. Such molecules have a favorable safety profile and are likely to allow the prolonged duration necessary for an efficient preventive strategy. Recent evidence on mechanisms and possible use is described here for food derivatives, including flavonoids, retinoids, triterpenoids, omega fatty acids, and carotenoids from marine microorganisms. As examples, a number of compounds, including epigallocatechin, resveratrol, xanthohumol, hydroxytyrosol, curcumin, fenretinide, lycopene, fucoxanthin, and repurposed drugs, such as aspirin, β blockers, renin–angiotensin–aldosterone inhibitors, carnitines, and biguanides, are reviewed.

Funder

Fondazione Umberto Veronesi

Fondazione Istituto Europeo di Oncologia e Centro Cardiologico Monzino

Ministero della Salute

Publisher

American Association for Cancer Research (AACR)

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