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Triparanol suppresses human tumor growth in vitro and in vivo.
Bi, Xinyu; Han, Xingpeng; Zhang, Fang; He, Miao; Zhang, Yi; Zhi, Xiu-Yi; Zhao, Hong.
Afiliación
  • Bi X; Department of Abdominal Surgical Oncology, Lab of Abdominal Surgical Oncology, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Biochem Biophys Res Commun ; 425(3): 613-8, 2012 Aug 31.
Article en En | MEDLINE | ID: mdl-22877755
ABSTRACT
Despite the improved contemporary multidisciplinary regimens treating cancer, majority of cancer patients still suffer from adverse effects and relapse, therefore posing a significant challenge to uncover more efficacious molecular therapeutics targeting signaling pathways central to tumorigenesis. Here, our study have demonstrated that Triparanol, a cholesterol synthesis inhibitor, can block proliferation and induce apoptosis in multiple human cancer cells including lung, breast, liver, pancreatic, prostate cancer and melanoma cells, and growth inhibition can be rescued by exogenous addition of cholesterol. Remarkably, we have proved Triparanol can significantly repress Hedgehog pathway signaling in these human cancer cells. Furthermore, study in a mouse xenograft model of human lung cancer has validated that Triparanol can impede tumor growth in vivo. We have therefore uncovered Triparanol as potential new cancer therapeutic in treating multiple types of human cancers with deregulated Hedgehog signaling.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Triparanol / Proteínas Hedgehog / Neoplasias / Hipolipemiantes / Antineoplásicos Límite: Animals / Female / Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2012 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Triparanol / Proteínas Hedgehog / Neoplasias / Hipolipemiantes / Antineoplásicos Límite: Animals / Female / Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2012 Tipo del documento: Article País de afiliación: China