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Interferon-Mediated Tumor Resistance to Oncolytic Virotherapy.
Ebrahimi, Safieh; Ghorbani, Elnaz; Khazaei, Majid; Avan, Amir; Ryzhikov, Mikhail; Azadmanesh, Kayhan; Hassanian, Seyed Mahdi.
Afiliação
  • Ebrahimi S; Department of Medical Biochemistry, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Ghorbani E; Department of Microbiology, Al-Zahra University, Tehran, Iran.
  • Khazaei M; Department of Medical Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Avan A; Metabolic Syndrome Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Ryzhikov M; Molecular Medicine Group, Department of Modern Sciences and Technologies, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Azadmanesh K; Department of Molecular Microbiology and Immunology, St. Louis University School of Medicine, Saint Louis, Missouri.
  • Hassanian SM; Virology Department, Pasteur Institute of Iran, Tehran, Iran.
J Cell Biochem ; 118(8): 1994-1999, 2017 08.
Article em En | MEDLINE | ID: mdl-28135008
Interferons (INFs) elicit antiviral responses in tumor cells upon binding to cell surface receptors. Oncolytic virotherapy (OV) is an effective antitumor therapeutic approach which in combination with standard radiotherapy or chemotherapy regimens potentiates treatment responses in cancer patients. However, oncolytic viruses are susceptible to the IFN-induced antiviral state in the tumor microenvironment. A number of studies have, therefore, investigated the effects of combined therapy of IFN signaling pharmacological inhibitors with oncolytic viruses, which result in improved virus replication and oncolysis. This review summarizes the current knowledge of the mechanisms of interferon-mediated tumor resistance to oncolytic virotherapy and provides new insights regarding the effectiveness of combinatorial treatment strategies to attenuate INF-induced OV resistance for greater clinical significance in the treatment of cancer patients. J. Cell. Biochem. 118: 1994-1999, 2017. © 2017 Wiley Periodicals, Inc.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Regulação Neoplásica da Expressão Gênica / Interferons / Terapia Viral Oncolítica / Nicho de Células-Tronco / Neoplasias Limite: Humans Idioma: En Revista: J Cell Biochem Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Irã

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Hematopoéticas / Regulação Neoplásica da Expressão Gênica / Interferons / Terapia Viral Oncolítica / Nicho de Células-Tronco / Neoplasias Limite: Humans Idioma: En Revista: J Cell Biochem Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Irã