Background Innovative treatment concepts targeting essential signaling pathways may offer new chances for patients suffering from cholangiocarcinoma (CCC). For that, we performed a systematic molecular genetic analysis concerning the Hedgehog activity in human CCC samples and analyzed the effect of Hh inhibition on CCC cells in vitro and in vivo. Methods Activation of the Hh pathway was analyzed in 50 human CCC samples using quantitative polymerase chain reaction (qPCR). The efficacy of Hh inhibition using cyclopamine and BMS-833923 was evaluated in vitro. In addition, the effect of BMS-833923, alone or in combination with gemcitabine, was analyzed in vivo in a murine subcutaneous xenograft model. Results Expression analysis revealed a significant activation of the Hh-signaling pathway in nearly 50% of CCCs. Hh inhibition resulted in a significant decrease in cell proliferation of CCC cells. Moreover, a distinct inhibition of tumor growth could be seen as a result of a combined therapy with BMS-833923 and gemcitabine in CCC xenografts. Conclusion The results of our study suggest that the Hh pathway plays a relevant role at least in a subset of human CCC. Inhibition of this pathway may represent a possible treatment option for CCC patients in which the Hh pathway is activated.
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Charles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech RepublicCharles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech Republic
Vickova, Katerina
Ondrusova, Lubica
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Charles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech RepublicCharles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech Republic
Ondrusova, Lubica
Reda, Jiri
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Charles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech RepublicCharles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech Republic
Reda, Jiri
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Vachtenheim, Jiri
Zakova, Petra
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Charles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech RepublicCharles Univ Prague, Inst Med Biochem, Fac Med 1, Prague 2, Czech Republic
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Univ Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USAUniv Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USA
Kumar, Virender
Dong, Yuxiang
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Univ Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USAUniv Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USA
Dong, Yuxiang
Kumar, Vinod
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Univ Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USAUniv Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USA
Kumar, Vinod
Almawash, Saud
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Univ Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USAUniv Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USA
Almawash, Saud
Mahato, Ram I.
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Univ Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USAUniv Nebraska Med Ctr, Dept Pharmaceut Sci, 986025 Nebraska Med Ctr, Omaha, NE 68198 USA
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Ohio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USAOhio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USA
Bhateja, Priyanka
Cherian, Mathew
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Ohio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USAOhio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USA
Cherian, Mathew
Majumder, Sarmila
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Ohio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USAOhio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USA
Majumder, Sarmila
Ramaswamy, Bhuvaneswari
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Ohio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USAOhio State Univ, James Comprehens Canc Ctr, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USA