Literature DB >> 15046708

Antimetastatic drugs in prostate cancer.

Christopher H Chay1, Carlton C Cooper, Beth A Hellerstedt, Kenneth J Pienta.   

Abstract

Despite the benefits of local therapy with radical prostatectomy and radiation, many patients with prostate cancer require hormonal ablation. While chemotherapy has proven efficacy when the disease progresses to androgen-independent prostate cancer, patients ultimately succumb to the disease, thus the identification of other active therapies is needed. Future treatment modalities include molecular targeted therapies. Prostate cancer has been an ideal model to study the multiple steps required in the metastatic cascade. These steps have been utilized in the development of metastasis inhibitors. This review will present promising agents that have been tested preclinically or are undergoing clinical investigation for their abilities in preventing prostate cancer metastasis. Because prostate cancer metastasizes preferentially to the bone, special attention will be given to agents that interfere with this pattern of metastasis. Specifically, the efficacy of angiogenesis inhibitors, metalloproteinase inhibitors, inhibitors of prostate cancer cell- endothelial cell interactions, and bisphosphonates will be reported. In addition, the introduction of these novel agents has raised many questions as to the relevance and optimal utilization of current clinical trial designs. Issues regarding combination therapy with chemotherapy, optimal timing of treatment with metastatic inhibitors, and the need for surrogate endpoints for molecular targeted therapies will be discussed.

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Year:  2002        PMID: 15046708     DOI: 10.3816/cgc.2002.n.002

Source DB:  PubMed          Journal:  Clin Prostate Cancer        ISSN: 1540-0352


  3 in total

1.  Anticancer and cytotoxic properties of the latex of Calotropis procera in a transgenic mouse model of hepatocellular carcinoma.

Authors:  Tenzin Choedon; Ganeshan Mathan; Soneera Arya; Vijay L Kumar; Vijay Kumar
Journal:  World J Gastroenterol       Date:  2006-04-28       Impact factor: 5.742

2.  U94 alters FN1 and ANGPTL4 gene expression and inhibits tumorigenesis of prostate cancer cell line PC3.

Authors:  Ekwere T Ifon; Alan L Y Pang; Warren Johnson; Kathleen Cashman; Sharon Zimmerman; Sumitra Muralidhar; Wai-Yee Chan; John Casey; Leonard Jason Rosenthal
Journal:  Cancer Cell Int       Date:  2005-06-22       Impact factor: 5.722

Review 3.  Changes in extracellular matrix (ECM) and ECM-associated proteins in the metastatic progression of prostate cancer.

Authors:  Delisha A Stewart; Carlton R Cooper; Robert A Sikes
Journal:  Reprod Biol Endocrinol       Date:  2004-01-07       Impact factor: 5.211

  3 in total

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