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HCMV modulation of cellular PI3K/AKT/mTOR signaling: New opportunities for therapeutic intervention?
Altman, Aaron M; Mahmud, Jamil; Nikolovska-Coleska, Zaneta; Chan, Gary.
  • Altman AM; Department of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
  • Mahmud J; Department of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
  • Nikolovska-Coleska Z; Department of Pathology, University of Michigan, Ann Arbor, MI 48109, USA.
  • Chan G; Department of Microbiology & Immunology, SUNY Upstate Medical University, Syracuse, NY 13210, USA. Electronic address: chang@upstate.edu.
Antiviral Res ; 163: 82-90, 2019 03.
Article en En | MEDLINE | ID: mdl-30668978
ABSTRACT
Human cytomegalovirus (HCMV) remains a major public health burden domestically and abroad. Current approved therapies, including ganciclovir, are only moderately efficacious, with many transplant patients suffering from a variety of side effects. A major impediment to the efficacy of current anti-HCMV drugs is their antiviral effects are restricted to the lytic stage of viral replication. Consequently, the non-lytic stages of the viral lifecycle remain major sources of HCMV infection associated with transplant recipients and ultimately the cause of morbidity and mortality. While work continues on new antivirals that block lytic replication, the dormant stages of HCMV's unique lifecycle need to be concurrently assessed for new therapeutic interventions. In this review, we will examine the role that the PI3K/Akt/mTOR signaling axis plays during the different stages of HCMV's lifecycle, and describe the advantages of targeting this cellular pathway as an antiviral strategy. In particular, we focus on the potential of exploiting the unique modifications HCMV imparts on the PI3K/Akt/mTOR pathway during quiescent infection of monocytes, which serve an essential role in the dissemination strategy of the virus.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Fosfatidilinositol 3-Quinasas / Citomegalovirus / Proteína Oncogénica v-akt / Interacciones Huésped-Patógeno / Serina-Treonina Quinasas TOR Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Fosfatidilinositol 3-Quinasas / Citomegalovirus / Proteína Oncogénica v-akt / Interacciones Huésped-Patógeno / Serina-Treonina Quinasas TOR Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article