Your browser doesn't support javascript.
loading
Preclinical safety evaluation of hepatic arterial infusion of oncolytic poxvirus.
Cho, Euna; Ryu, Eun Jin; Jiang, Fen; Jeon, Ung Bae; Cho, Mong; Kim, Cy Hyun; Kim, Miyoung; Kim, Nam Deuk; Hwang, Tae-Ho.
Afiliación
  • Cho E; Department of Pharmacology and Medical Research Center (MRC), Pusan National University School of Medicine, Yangsan, Korea, thhwang@pusan.ac.kr.
  • Ryu EJ; Department of Research and Development, Bionoxx Inc, Seongnam-si, Korea, thhwang@pusan.ac.kr.
  • Jiang F; Department of Research and Development, Bionoxx Inc, Seongnam-si, Korea, thhwang@pusan.ac.kr.
  • Jeon UB; Department of Radiology, Pusan National University Yangsan Hospital, Yangsan, Korea.
  • Cho M; Department of Research and Development, Bionoxx Inc, Seongnam-si, Korea, thhwang@pusan.ac.kr.
  • Kim CH; School of Pharmaceutical Science (Shenzhen), Sun Yat-sen University, Guangzhou, China.
  • Kim M; Department of Radiology, Pusan National University Yangsan Hospital, Yangsan, Korea.
  • Kim ND; Department of Pharmacology and Medical Research Center (MRC), Pusan National University School of Medicine, Yangsan, Korea, thhwang@pusan.ac.kr.
  • Hwang TH; Department of Research and Development, Bionoxx Inc, Seongnam-si, Korea, thhwang@pusan.ac.kr.
Drug Des Devel Ther ; 12: 2467-2474, 2018.
Article en En | MEDLINE | ID: mdl-30122903
PURPOSE: Oncolytic poxvirus has shown promise in treating various solid tumors, such as liver cancer, and administration of oncolytic poxvirus via the hepatic artery may provide more survival benefits than other routes of administration. However, there is a lack of safety information to guide the application of hepatic arterial infusion (HAI) of oncolytic poxvirus in human studies. To investigate the acute and chronic toxicity of HAI administration of oncolytic poxvirus in animals and provide safety information for future human studies. METHODS: VVtk-, a vaccinia poxvirus with inactivated thymidine kinase gene, was administered via HAI to rabbits with normal liver function under angiography (1×108 or 1×109 pfu), and rats with N-nitrosomorpholine-induced precancerous liver cirrhosis under open surgery (1×108 pfu). Body weights and survival were monitored and blood samples were collected for hematological and biochemical tests. Distribution of A56 (a specific marker for poxvirus infection) in rabbit organs was evaluated using immunofluorescence assays. RESULTS: HAI of high doses of VVtk- did not cause any acute or chronic changes in body weight, survival or in biochemical, hematological tests in the 2 animal models, and none of the changes showed dose dependency (in rabbit study), or were influenced by liver cirrhosis (in rat study). A56 was not detected in any of the major rabbit organs. CONCLUSION: HAI may provide a safe alternative route of oncolytic poxvirus administration for human studies.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Poxviridae / Viroterapia Oncolítica / Neoplasias Hepáticas Límite: Animals Idioma: En Revista: Drug Des Devel Ther Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2018 Tipo del documento: Article Pais de publicación: Nueva Zelanda

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Poxviridae / Viroterapia Oncolítica / Neoplasias Hepáticas Límite: Animals Idioma: En Revista: Drug Des Devel Ther Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2018 Tipo del documento: Article Pais de publicación: Nueva Zelanda