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LY2109761, a novel transforming growth factor beta receptor type I and type II dual inhibitor, as a therapeutic approach to suppressing pancreatic cancer metastasis.
Melisi, Davide; Ishiyama, Satoshi; Sclabas, Guido M; Fleming, Jason B; Xia, Qianghua; Tortora, Giampaolo; Abbruzzese, James L; Chiao, Paul J.
Afiliação
  • Melisi D; Department of Gastrointestinal Medical Oncology, The University of Texas M.D.Anderson Cancer Center, Houston, Texas 77030, USA.
Mol Cancer Ther ; 7(4): 829-40, 2008 Apr.
Article em En | MEDLINE | ID: mdl-18413796
Most pancreatic cancer patients present with inoperable disease or develop metastases after surgery. Conventional therapies are usually ineffective in treating metastatic disease. It is evident that novel therapies remain to be developed. Transforming growth factor beta (TGF-beta) plays a key role in cancer metastasis, signaling through the TGF-beta type I/II receptors (TbetaRI/II). We hypothesized that targeting TbetaRI/II kinase activity with the novel inhibitor LY2109761 would suppress pancreatic cancer metastatic processes. The effect of LY2109761 has been evaluated on soft agar growth, migration, invasion using a fibroblast coculture model, and detachment-induced apoptosis (anoikis) by Annexin V flow cytometric analysis. The efficacy of LY2109761 on tumor growth, survival, and reduction of spontaneous metastasis have been evaluated in an orthotopic murine model of metastatic pancreatic cancer expressing both luciferase and green fluorescence proteins (L3.6pl/GLT). To determine whether pancreatic cancer cells or the cells in the liver microenvironment were involved in LY2109761-mediated reduction of liver metastasis, we used a model of experimental liver metastasis. LY2109761 significantly inhibited the L3.6pl/GLT soft agar growth, suppressed both basal and TGF-beta1-induced cell migration and invasion, and induced anoikis. In vivo, LY2109761, in combination with gemcitabine, significantly reduced the tumor burden, prolonged survival, and reduced spontaneous abdominal metastases. Results from the experimental liver metastasis models indicate an important role for targeting TbetaRI/II kinase activity on tumor and liver microenvironment cells in suppressing liver metastasis. Targeting TbetaRI/II kinase activity on pancreatic cancer cells or the cells of the liver microenvironment represents a novel therapeutic approach to prevent pancreatic cancer metastasis.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Pirazóis / Pirróis / Proteínas Serina-Treonina Quinases / Receptores de Fatores de Crescimento Transformadores beta / Inibidores de Proteínas Quinases / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Idioma: En Revista: Mol Cancer Ther Assunto da revista: ANTINEOPLASICOS Ano de publicação: 2008 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Pirazóis / Pirróis / Proteínas Serina-Treonina Quinases / Receptores de Fatores de Crescimento Transformadores beta / Inibidores de Proteínas Quinases / Neoplasias Pulmonares Tipo de estudo: Prognostic_studies Idioma: En Revista: Mol Cancer Ther Assunto da revista: ANTINEOPLASICOS Ano de publicação: 2008 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos