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Reovirus safety study for proliferation and differentiation of human adipose-derived mesenchymal stem cells
Jeong-Soo Park , Manbok Kim
J. Microbiol. 2017;55(1):75-79.   Published online December 30, 2016
DOI: https://doi.org/10.1007/s12275-017-6542-0
  • 49 View
  • 0 Download
  • 8 Crossref
AbstractAbstract
Naturally occurring reoviruses are live replication-proficient viruses specifically infecting human cancer cells while sparing the normal counterparts. Stem cells can be highly susceptible to viral infection due to their innate high proliferation potential and other active signaling pathways of cells that might be involved in viral tropism. In the previous study, we showed that reoviruses could adversely affect murine embryonic stem cells’ integrity in vitro and in vivo. Oncolytic viruses, delivered systemically face many hurdles that also impede their localization and infection of, metastatic tumors, due to a variety of immune and physical barriers. To overcome such hurdles to systemic delivery, several studies supported the idea that certain types of cells, including mesenchymal stem cells, might play a role as cell carriers for oncolytic viruses. Thus, it would be interesting to examine whether human adult stem cells such as human adipose-derived mesenchymal stem cells could be saved by the reoviral challenge. In this study, we report that biological activities such as proliferation and multipotency of human adipose-derived stem cells are not affected by wild-type reovirus challenge as evidenced by survival, osteogenic and adipogenic differentiation potential assays following treatment with reoviruses. Therefore, unlike murine embryonic stem cells, our study strongly suggests that human adipose-derived adult stem cells could be spared in vivo during wild-type reoviral anti-cancer therapeutics in a clinical setting. Furthermore, the results support the possible clinical use of human adipose-derived stem cells as an effective cell carrier of oncolytic reovirus to maximize their tumor tropism and anti-tumor activity.

Citations

Citations to this article as recorded by  
  • Modulation of Reoviral Cytolysis (II): Cellular Stemness
    Tarryn Bourhill, Leili Rohani, Mehul Kumar, Pinaki Bose, Derrick Rancourt, Randal N. Johnston
    Viruses.2023; 15(7): 1473.     CrossRef
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  • Mesenchymal stem cells support delivery and boost the efficacy of oncolytic reoviruses in TC‐1 tumor cells
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    Journal of Cellular Biochemistry.2021; 122(10): 1360.     CrossRef
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    European Journal of Pharmacology.2020; 874: 172991.     CrossRef
  • Recent advances in targeting cancer stem cells using oncolytic viruses
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    Biotechnology Letters.2020; 42(6): 865.     CrossRef
  • The oncolytic efficacy and safety of avian reovirus and its dynamic distribution in infected mice
    Ruimin Cai, Guangyuan Meng, Yi Li, Wenyang Wang, Youxiang Diao, Shuping Zhao, Qiang Feng, Yi Tang
    Experimental Biology and Medicine.2019; 244(12): 983.     CrossRef
  • Going (Reo)Viral: Factors Promoting Successful Reoviral Oncolytic Infection
    Tarryn Bourhill, Yoshinori Mori, Derrick Rancourt, Maya Shmulevitz, Randal Johnston
    Viruses.2018; 10(8): 421.     CrossRef
  • Primary lymphocyte infection models for KSHV and its putative tumorigenesis mechanisms in B cell lymphomas
    Sangmin Kang, Jinjong Myoung
    Journal of Microbiology.2017; 55(5): 319.     CrossRef
Review
Replicating poxviruses for human cancer therapy
Manbok Kim
J. Microbiol. 2015;53(4):209-218.   Published online April 8, 2015
DOI: https://doi.org/10.1007/s12275-015-5041-4
  • 57 View
  • 0 Download
  • 24 Crossref
AbstractAbstract
Naturally occurring oncolytic viruses are live, replicationproficient viruses that specifically infect human cancer cells while sparing normal cell counterparts. Since the eradication of smallpox in the 1970s with the aid of vaccinia viruses, the vaccinia viruses and other genera of poxviruses have shown various degrees of safety and efficacy in pre-clinical or clinical application for human anti-cancer therapeutics. Furthermore, we have recently discovered that cellular tumor suppressor genes are important in determining poxviral oncolytic tropism. Since carcinogenesis is a multi-step process involving accumulation of both oncogene and tumor suppressor gene abnormalities, it is interesting that poxvirus can exploit abnormal cellular tumor suppressor signaling for its oncolytic specificity and efficacy. Many tumor suppressor genes such as p53, ATM, and RB are known to play important roles in genomic fidelity/maintenance. Thus, tumor suppressor gene abnormality could affect host genomic integrity and likely disrupt intact antiviral networks due to accumulation of genetic defects, which would in turn result in oncolytic virus susceptibility. This review outlines the characteristics of oncolytic poxvirus strains, including vaccinia, myxoma, and squirrelpox virus, recent progress in elucidating the molecular connection between oncogene/tumor suppressor gene abnormalities and poxviral oncolytic tropism, and the associated preclinical/clinical implications. I would also like to propose future directions in the utility of poxviruses for oncolytic virotherapy.

Citations

Citations to this article as recorded by  
  • Tutorial: design, production and testing of oncolytic viruses for cancer immunotherapy
    Shashi Gujar, Jonathan G. Pol, Vishnupriyan Kumar, Manuela Lizarralde-Guerrero, Prathyusha Konda, Guido Kroemer, John C. Bell
    Nature Protocols.2024; 19(9): 2540.     CrossRef
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    Yanrong Zhou, Qianpeng Wang, Qi Ying, Xiaomei Zhang, Ting Ye, Kan Chen, Gongchu Li
    Marine Drugs.2023; 21(2): 77.     CrossRef
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    Therapeutic Advances in Infectious Disease.2022;[Epub]     CrossRef
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    Infection, Genetics and Evolution.2022; 98: 105220.     CrossRef
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    Hajime Kurosaki, Motomu Nakatake, Teruhisa Sakamoto, Nozomi Kuwano, Masato Yamane, Kenta Ishii, Yoshiyuki Fujiwara, Takafumi Nakamura
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  • Oncolytic Vaccinia Virus Expressing White-Spotted Charr Lectin Regulates Antiviral Response in Tumor Cells and Inhibits Tumor Growth In Vitro and In Vivo
    Xue Wang, Ningning Zhou, Tingting Liu, Xiaoyuan Jia, Ting Ye, Kan Chen, Gongchu Li
    Marine Drugs.2021; 19(6): 292.     CrossRef
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    Su-Nam Jeong, So Young Yoo
    Cancers.2020; 12(5): 1070.     CrossRef
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    Yuhui Zhang, Zhuoming Liu
    Current Pharmaceutical Design.2020; 25(40): 4251.     CrossRef
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    James B. Eaglesham, Youdong Pan, Thomas S. Kupper, Philip J. Kranzusch
    Nature.2019; 566(7743): 259.     CrossRef
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    Expert Opinion on Biological Therapy.2019; 19(6): 561.     CrossRef
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    A. V. Tkacheva, G. F. Sivolobova, A. A. Grazhdantseva, O. B. Shevelev, I. A. Razumov, E. L. Zavjalov, V. B. Loktev, G. V. Kochneva
    Molecular Genetics, Microbiology and Virology.2019; 34(2): 140.     CrossRef
  • Intra-tumoral delivery of CXCL11 via a vaccinia virus, but not by modified T cells, enhances the efficacy of adoptive T cell therapy and vaccines
    Edmund K. Moon, Liang-Chuan S. Wang, Kheng Bekdache, Rachel C. Lynn, Albert Lo, Stephen H. Thorne, Steven M. Albelda
    OncoImmunology.2018; 7(3): e1395997.     CrossRef
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    Michael White, Andrew Freistaedter, Gwendolyn J. B. Jones, Emmanuel Zervos, Rachel L. Roper, Aamir Ahmad
    PLOS ONE.2018; 13(2): e0193131.     CrossRef
  • Mutagenic repair of double-stranded DNA breaks in vaccinia virus genomes requires cellular DNA ligase IV activity in the cytosol
    Rutger David Luteijn, Ingo Drexler, Geoffrey L. Smith, Robert Jan Lebbink, Emmanuel J. H. J. Wiertz
    Journal of General Virology.2018; 99(6): 790.     CrossRef
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    Yogesh R. Suryawanshi, Tiantian Zhang, Karim Essani
    Medical Oncology.2017;[Epub]     CrossRef
  • Primary lymphocyte infection models for KSHV and its putative tumorigenesis mechanisms in B cell lymphomas
    Sangmin Kang, Jinjong Myoung
    Journal of Microbiology.2017; 55(5): 319.     CrossRef
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    Journal of Translational Medicine.2016;[Epub]     CrossRef
  • Oncolytic virotherapy for urological cancers
    Zahid Delwar, Kaixin Zhang, Paul S. Rennie, William Jia
    Nature Reviews Urology.2016; 13(6): 334.     CrossRef
  • Features of the Antitumor Effect of Vaccinia Virus Lister Strain
    Evgeniy Zonov, Galina Kochneva, Anastasiya Yunusova, Antonina Grazhdantseva, Vladimir Richter, Elena Ryabchikova
    Viruses.2016; 8(1): 20.     CrossRef
  • Single-particle characterization of oncolytic vaccinia virus by flow virometry
    Vera A. Tang, Tyler M. Renner, Oliver Varette, Fabrice Le Boeuf, Jiahu Wang, Jean-Simon Diallo, John C. Bell, Marc-André Langlois
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    Viruses.2016; 8(5): 134.     CrossRef
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    Manbok Kim
    BMB Reports.2015; 48(8): 454.     CrossRef
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    Manbok Kim
    Journal of Bacteriology and Virology.2015; 45(2): 126.     CrossRef

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