www.oncotarget.com Oncotarget, 2020, Vol. 11, (No. 51), pp: 4693-4698 Research Paper NSCs are permissive to oncolytic Myxoma virus and provide a delivery method for targeted ovarian cancer therapy Yvonne Cornejo1,2, Min Li3, Thanh H. Dellinger4, Rachael Mooney1, Masmudur M. Rahman5, Grant McFadden5, Karen S. Aboody1,6 and Mohamed Hammad1 1Department of Stem Cell & Developmental Biology, City of Hope, Duarte, CA 91010, USA 2Irell & Manella Graduate School for Biological Sciences, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA 3Department of Information Sciences, Division of Biostatistics at the Beckman Research Institute, City of Hope, Duarte, CA 91010, USA 4Division of Gynecologic Surgery, Department of Surgery, City of Hope, CA 91010, USA 5Biodesign Institute, Arizona State University, Tempe, AZ 85281, USA 6Division of Neurosurgery, City of Hope, Duarte, CA 91010, USA Correspondence to: Mohamed Hammad, email:
[email protected] Keywords: oncolytic virotherapy; myxoma; NSCs; ovarian cancer Received: October 09, 2020 Accepted: December 03, 2020 Published: December 22, 2020 Copyright: © 2020 Cornejo et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. ABSTRACT Despite the development of many anticancer agents over the past 20 years, ovarian cancer remains the most lethal gynecologic malignancy. Due to a lack of effective screening, the majority of patients with ovarian cancer are diagnosed at an advanced stage, and only ~20% of patients are cured. Thus, in addition to improved screening methods, there is an urgent need for novel anticancer agents that are effective against late-stage, metastatic disease.