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ASP5878, a Novel Inhibitor of FGFR1, 2, 3, and 4, Inhibits the Growth of FGF19-Expressing Hepatocellular Carcinoma.
Futami, Takashi; Okada, Hidetsugu; Kihara, Rumi; Kawase, Tatsuya; Nakayama, Ayako; Suzuki, Tomoyuki; Kameda, Minoru; Shindoh, Nobuaki; Terasaka, Tadashi; Hirano, Masaaki; Kuromitsu, Sadao.
Afiliação
  • Futami T; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan. takashi.futami@astellas.com.
  • Okada H; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Kihara R; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Kawase T; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Nakayama A; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Suzuki T; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Kameda M; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Shindoh N; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Terasaka T; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Hirano M; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
  • Kuromitsu S; Drug Discovery Research, Astellas Pharma Inc., Ibaraki, Japan.
Mol Cancer Ther ; 16(1): 68-75, 2017 01.
Article em En | MEDLINE | ID: mdl-27837028
Hepatocellular carcinoma is an aggressive cancer with poor prognosis. Fibroblast growth factor 19, a member of the fibroblast growth factor family, is a ligand for fibroblast growth factor receptor 4. Moreover, it plays a crucial role in the progression of hepatocellular carcinoma. ASP5878 is a novel inhibitor of fibroblast growth factor receptors 1, 2, 3, and 4 that is under development. It inhibits fibroblast growth factor receptor 4 kinase activity with an IC50 of 3.5 nmol/L. ASP5878 potently suppressed the growth of the fibroblast growth factor 19-expressing hepatocellular carcinoma cell lines Hep3B2.1-7, HuH-7, and JHH-7. In the Hep3B2.1-7 cell line, ASP5878 inhibited the phosphorylation of fibroblast growth factor receptor 4 and its downstream signaling molecules as well as induced apoptosis. Oral administration of ASP5878 at 3 mg/kg induced sustained tumor regression in a subcutaneous xenograft mouse model using Hep3B2.1-7. In HuH-7, an orthotopic xenograft mouse model, ASP5878 induced complete tumor regression and dramatically extended the survival of the mice. These results suggest that ASP5878 is a potentially effective therapeutic agent for hepatocellular carcinoma patients with tumors expressing fibroblast growth factor 19. Mol Cancer Ther; 16(1); 68-75. ©2016 AACR.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirazóis / Pirimidinas / Expressão Gênica / Receptores de Fatores de Crescimento de Fibroblastos / Carcinoma Hepatocelular / Fatores de Crescimento de Fibroblastos / Neoplasias Hepáticas / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Mol Cancer Ther Assunto da revista: ANTINEOPLASICOS Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirazóis / Pirimidinas / Expressão Gênica / Receptores de Fatores de Crescimento de Fibroblastos / Carcinoma Hepatocelular / Fatores de Crescimento de Fibroblastos / Neoplasias Hepáticas / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Animals / Humans / Male Idioma: En Revista: Mol Cancer Ther Assunto da revista: ANTINEOPLASICOS Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Japão