Literature DB >> 16622744

Current status and perspective of antiangiogenic therapy for cancer: urinary cancer.

Shigeru Kanda1, Yasuyoshi Miyata, Hiroshi Kanetake.   

Abstract

Angiogenesis is considered a prerequisite for solid tumor growth. Antiangiogenic therapy reduces tumor size and extends host survival in a number of preclinical animal models. However, in humans antiangiogenic therapy is a poor promoter of tumor regression and has shown minimal effect on patient survival. In urinary cancers, such as renal cell cancer, prostate cancer, and bladder cancer, advanced refractory disease is a good candidate for antiangiogenic therapy because of its resistance to ordinary chemotherapy, radiotherapy, and hormonal therapy. Unique characteristics of molecular mechanisms underlie the induction of angiogenesis in urinary cancers. In this review, we summarize these unique mechanisms and review the results of clinical trials of antiangiogenic therapy for these cancers, discussing prospects and problems relating to antiangiogenic therapy.

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Year:  2006        PMID: 16622744     DOI: 10.1007/s10147-006-0565-6

Source DB:  PubMed          Journal:  Int J Clin Oncol        ISSN: 1341-9625            Impact factor:   3.850


  265 in total

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Journal:  Cancer       Date:  2005-12-01       Impact factor: 6.860

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Journal:  Nature       Date:  1997-11-27       Impact factor: 49.962

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Journal:  Cancer Res       Date:  1993-06-01       Impact factor: 12.701

6.  Inhibition of hemangiogenesis and lymphangiogenesis after normal-risk corneal transplantation by neutralizing VEGF promotes graft survival.

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Journal:  Invest Ophthalmol Vis Sci       Date:  2004-08       Impact factor: 4.799

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Journal:  J Biol Chem       Date:  1996-02-16       Impact factor: 5.157

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Authors:  Walter M Stadler; Dingcai Cao; Nicholas J Vogelzang; Christopher W Ryan; Kristin Hoving; Russell Wright; Theodore Karrison; Everett E Vokes
Journal:  Clin Cancer Res       Date:  2004-05-15       Impact factor: 12.531

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Authors:  D M Ornitz; N Itoh
Journal:  Genome Biol       Date:  2001-03-09       Impact factor: 13.583

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Journal:  J Exp Med       Date:  1995-07-01       Impact factor: 14.307

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  1 in total

1.  Downregulation of the c-Fes protein-tyrosine kinase inhibits the proliferation of human renal carcinoma cells.

Authors:  Shigeru Kanda; Yasuyoshi Miyata; Hiroshi Kanetake; Thomas E Smithgall
Journal:  Int J Oncol       Date:  2009-01       Impact factor: 5.650

  1 in total

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