Literature DB >> 19617926

VEGF inhibitors and prostate cancer therapy.

Jeanny B Aragon-Ching1, William L Dahut.   

Abstract

Prostate cancer remains the most common non-cutaneous malignancy among American men. Since the advent of PSA testing, most men are diagnosed with localized disease, but a proportion of men will be diagnosed with metastatic disease, many will eventually receive chemotherapy with docetaxel and prednisone. However, responses are not durable and all men will ultimately progress on this treatment. As such, continued efforts are geared towards the discovery of new agents and mechanisms of targeting prostate cancer. Angiogenesis has been shown to play an important role in tumorigenesis, proliferation and metastasis in prostate cancer. Here we discuss the major angiogenic signaling pathway involving VEGF in prostate cancer progression and the role of various promising agents that targets this pathway. This includes bevacizumab, thalidomide and its analogues, tyrosine kinase inhibitors sorafenib and AZD2171, and other inhibitors of angiogenic signaling pathways. Results of key clinical trials associated with the use of these agents and future directions are discussed herein.

Entities:  

Keywords:  AZD2171; Angiogenesis; Bevacizumab; Lenalidomide; Prostate Cancer; Sorafenib; Thalidomide

Mesh:

Substances:

Year:  2009        PMID: 19617926      PMCID: PMC2711630          DOI: 10.2174/1874467210902020161

Source DB:  PubMed          Journal:  Curr Mol Pharmacol        ISSN: 1874-4672            Impact factor:   3.339


  71 in total

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  21 in total

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5.  Different roles of myofibroblasts in the tumorigenesis of nonsmall cell lung cancer.

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9.  Saracatinib as a metastasis inhibitor in metastatic castration-resistant prostate cancer: A University of Chicago Phase 2 Consortium and DOD/PCF Prostate Cancer Clinical Trials Consortium Study.

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