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Rapamycin potenziert die Wirkung von 5-FU beim Thymidinphosphorylase exprimierenden kolorektalen Karzinom durch Inhibition 2-deoxy-D-Ribose vermittelter Angiogenese

Rapamycin optimizes 5-FU effects on thymidine phosphorylase expressing colorectal cancer by inhibition of 2-deoxy-D-ribose mediated angiogenesis

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Chirurgisches Forum 2004

Part of the book series: Deutsche Gesellschaft für Chirurgie ((FORUMBAND,volume 33))

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Abstract

In colorectal cancer and other malignancies, thymidine phosphorylase (TP) activates 5-fluorouracil (5-FU) while promoting tumor angiogenesis at the same time via the generation of 2-deoxy-D-ribose (dRib). Here, we show that addition of rapamycin, an immunosuppressive agent with newly discovered antiangiogenic properties, to 5-FU cytotoxic chemotherapy strongly suppresses orthothopic and metastatic colon tumor growth in mice. Moreover, in vitro results from Boyden chamber and aortic ring experiments demonstrate that rapamycin inhibits different steps of TP/dRib-induced angiogenesis. Taken together, the combination of 5-FU with rapamycin may be a promising approach in advanced colorectal cancer.

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Correspondence to H. Seeliger .

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© 2004 Springer-Verlag Berlin Heidelberg

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Seeliger, H., Guba, M., Koehl, G., Bruns, C.J., Jauch, K.W., Geissler, E.K. (2004). Rapamycin potenziert die Wirkung von 5-FU beim Thymidinphosphorylase exprimierenden kolorektalen Karzinom durch Inhibition 2-deoxy-D-Ribose vermittelter Angiogenese. In: Ulrich, B., Jauch, KW., Bauer, H., Menger, M.D., Laschke, M., Slotta, J. (eds) Chirurgisches Forum 2004. Deutsche Gesellschaft für Chirurgie, vol 33. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-18547-2_10

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  • DOI: https://doi.org/10.1007/978-3-642-18547-2_10

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-20027-7

  • Online ISBN: 978-3-642-18547-2

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