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- W2013201726 abstract "Angiogenesis is a complex biological phenomenon that forms new blood vessels from the pre-existing vasculature. Aberrant angiogenesis has been implicated in a variety of diseases such as cancer, atherosclerosis, arthritis, obesity, pulmonary hypertension, diabetic retinopathy, and age-related macular degeneration. These conditions collectively affect nearly 10% of the global population. Much effort has focused on identifying new therapeutic agents that inhibit pathological angiogenesis since 1971, when Judah Folkman published the hypothesis that tumor growth is angiogenesis-dependent and that its inhibition may be therapeutic. In 2004, the U.S. Food and Drug Administration approved the first antiangiogenic drug for the treatment of metastatic colon cancer, bevacizumab (Avastin, Genentech). This drug is a humanized monoclonal antibody that neutralizes the vascular endothelial growth factor. It is used in combination with chemotherapy, and its use began the era of antiangiogenesis therapy. Several new therapeutic agents have been added to the list of approved drugs, and clinical trials of new therapeutic options and antiangiogenic agents are ongoing. This review describes the progress made in the first decade of antiangiogenesis therapy, and addresses both validated and possible targets for future drug development." @default.
- W2013201726 created "2016-06-24" @default.
- W2013201726 creator A5040740483 @default.
- W2013201726 date "2014-01-01" @default.
- W2013201726 modified "2023-09-26" @default.
- W2013201726 title "Antiangiogenesis therapy: an update after the first decade" @default.
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- W2013201726 doi "https://doi.org/10.3904/kjim.2014.29.1.1" @default.
- W2013201726 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3932378" @default.
- W2013201726 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24574826" @default.
- W2013201726 hasPublicationYear "2014" @default.
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