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Review
. 2003;33(1):79-88.
doi: 10.1385/IJGC:33:1:79.

Angiogenesis and antiangiogenic strategies in pancreatic cancer

Affiliations
Review

Angiogenesis and antiangiogenic strategies in pancreatic cancer

William E Fisher et al. Int J Gastrointest Cancer. 2003.

Abstract

Despite numerous advances in the treatment of solid tumors, the prognosis of patients diagnosed with pancreatic cancer remains dismal. Results of both surgical and non-surgical treatment for pancreatic cancer have been extremely disappointing because of the tumors propensity to metastasize, failure of chemotherapy to achieve adequate levels within the tumor, and resistance of pancreatic cancer to cytotoxic agents. Current chemotherapeutic agents and radiation treatments rely on the rapidly dividing nature of tumor cells and are limited by their cytotoxic effects on normal cells. The need to exploit the difference between normal and malignant cells has resulted in an enormous amount of research into the process of tumor neovascularization. New agents are currently being developed that block tumor growth and metastasis through inhibition of angiogenesis. This article reviews the process of angiogenesis and antiangiogenic strategies with a special emphasis on pancreatic cancer.

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References

    1. Biochem Biophys Res Commun. 1993 Aug 16;194(3):1234-41 - PubMed
    1. Nat Med. 1996 Jun;2(6):689-92 - PubMed
    1. Science. 1994 Apr 22;264(5158):569-71 - PubMed
    1. J Clin Invest. 1993 Dec;92(6):2756-60 - PubMed
    1. J Biol Chem. 1987 Mar 25;262(9):4098-103 - PubMed

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