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©2007 Baishideng Publishing Group Co.
World J Gastroenterol. Sep 21, 2007; 13(35): 4761-4770
Published online Sep 21, 2007. doi: 10.3748/wjg.v13.i35.4761
Published online Sep 21, 2007. doi: 10.3748/wjg.v13.i35.4761
Figure 3 In vivo treatment with NVP-LBH589 ± gemcitabine in chimeric mice.
A: Effect on tumor volume of EGI-1 cells (aP < 0.05, NVP-LBH589 vs control; cP < 0.05, COMBO vs control); B: Effect on tumor volume of Mz-ChA-2 cells (aP < 0.05, bP < 0.01, NVP-LBH589 vs control; cP < 0.05, dP < 0.01, COMBO vs control; fP < 0.01, gemcitabine vs control); C: Effect on tumor mass (aP < 0.05, NVP-LBH589 or COMBO vs control; bP < 0.01, NVP-LBH589 or COMBO or gemcitabine vs control).
- Citation: Bluethner T, Niederhagen M, Caca K, Serr F, Witzigmann H, Moebius C, Mossner J, Wiedmann M. Inhibition of histone deacetylase for the treatment of biliary tract cancer: A new effective pharmacological approach. World J Gastroenterol 2007; 13(35): 4761-4770
- URL: https://www.wjgnet.com/1007-9327/full/v13/i35/4761.htm
- DOI: https://dx.doi.org/10.3748/wjg.v13.i35.4761