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

血管生成 癌症预防 癌症 医学 药理学 保健品 苏林达克 姜黄素 羟基酪醇 转移 岩藻黄质 白藜芦醇 索拉非尼 癌症研究 内科学 抗氧化剂 化学 生物化学 类胡萝卜素 病理 肝细胞癌 非甾体 多酚
作者
Adriana Albini,Douglas M. Noonan,Paola Corradino,Francesca Magnoni,Giovanni Corso
出处
期刊:Cancer Prevention Research [American Association for Cancer Research]
卷期号:17 (7): 289-303 被引量:12
标识
DOI:10.1158/1940-6207.capr-24-0085
摘要

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.
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