Amanda L. Huff, Phonphimon Wongthida, T. Kottke, Jill Thompson, C. Driscoll, M. Schuelke, Kevin G. Shim, R. Harris, Amy M. Molan, J. Pulido, P. Selby, K. Harrington, A. Melcher, Laura Evgin, R. Vile
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引用次数: 0
Abstract
Tumor cells are able to evade cytotoxic therapies through the accumulation of genomic mutations and rapid evolution. In the case of oncolytic virotherapy, understanding the mechanisms by which cancer cells develop resistance to infection and lysis is critical to the development of more effective viral-based platforms. Here, we identify APOBEC3 as an important factor involved in the restriction of vesicular stomatitis virus (VSV). We show that VSV infection of B16 murine melanoma cells upregulated APOBEC3 in an IFNβ-dependent manner, which was responsible for the evolution of virus-resistanT-cell populations and suggested that APOBEC3 expression promoted the acquisition of a virus-resistant phenotype. ShRNA knockdown of APOBEC3 in B16 cells diminished their capacity to develop resistance to VSV infection in vitro, and enhanced the therapeutic effect of VSV in vivo. Similarly, overexpression of human APOBEC3B promoted the acquisition of resistance to oncolytic VSV in murine melanoma and glioblastoma lines, as well as in a human melanoma cell line in vitro and in vivo. Finally, we demonstrate that progeny virus obtained after passage through APOBEC3B overexpressing cells contained more defective interfering particles, thereby indicating that APOBEC3B directly affected the fitness of VSV, an RNA virus that has not previously been identified to be restricted by APOBEC3B. This research identifies APOBEC3 enzymes as key players to target in order to improve the efficacy of oncolytic viruses as well as broader nucleic acid-based therapeutic platforms. Citation Format: Amanda L. Huff, Phonphimon Wongthida, Timothy Kottke, Jill Thompson, Christopher B. Driscoll, Matthew Schuelke, Kevin G. Shim, Reuben S. Harris, Amy Molan, Jose S. Pulido, Peter J. Selby, Kevin J. Harrington, Alan Melcher, Laura Evgin, Richard Vile. APOBEC3 confers resistance to oncolytic VSV therapy [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A133.
肿瘤细胞能够通过基因组突变的积累和快速进化来逃避细胞毒性治疗。就溶瘤病毒治疗而言,了解癌细胞对感染和裂解产生抗性的机制对于开发更有效的基于病毒的平台至关重要。在这里,我们确定APOBEC3是参与限制水疱性口炎病毒(VSV)的一个重要因素。我们发现VSV感染B16小鼠黑色素瘤细胞以ifn β依赖的方式上调APOBEC3,这与病毒抗性细胞群体的进化有关,并表明APOBEC3的表达促进了病毒抗性表型的获得。ShRNA敲低B16细胞的APOBEC3,在体外降低了B16细胞对VSV感染的抗性,在体内增强了VSV的治疗效果。同样,人APOBEC3B的过表达促进了小鼠黑色素瘤和胶质母细胞瘤细胞系以及人黑色素瘤细胞系在体外和体内获得对溶瘤性VSV的抗性。最后,我们证明通过APOBEC3B过表达细胞获得的子代病毒含有更多有缺陷的干扰颗粒,从而表明APOBEC3B直接影响VSV的适应度,而VSV是一种以前未被鉴定为受APOBEC3B限制的RNA病毒。本研究确定了APOBEC3酶作为关键靶点,以提高溶瘤病毒的疗效以及更广泛的基于核酸的治疗平台。引文格式:Amanda L. Huff, Phonphimon Wongthida, Timothy Kottke, Jill Thompson, Christopher B. Driscoll, Matthew Schuelke, Kevin G. Shim, Reuben S. Harris, Amy Molan, Jose S. Pulido, Peter J. Selby, Kevin J. Harrington, Alan Melcher, Laura Evgin, Richard Vile。APOBEC3赋予对溶瘤性VSV治疗的抗性[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫,2019;7(2增刊):摘要nr A133。