Enhancement of oncolytic flavi- and alphavirus replication in resistant human pancreatic adenocarcinoma cell lines using ruxolitinib.

Q3 Medicine
K N Trachuk, Y K Biryukova, V А Kapranov, E A Orlova, A S Nazarenko, N M Kolyasnikova
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引用次数: 0

Abstract

Introduction: Overcoming the immunosuppressive microenvironment of pancreatic cancer (PC) using oncolytic viruses appears to be a promising therapeutic approach. However, tumor cells are characterized by significant heterogeneity, including populations of resistant cells with high basal JAK/STAT signaling activity. One potential approach to overcoming this resistance is the use of JAK1/2 kinase inhibitors, such as ruxolitinib, the efficacy of which has already been demonstrated in several studies.

Objective: To study the effect of ruxolitinib (a JAK1/2 kinase inhibitor) on the replicative activity of certain oncolytic flaviviruses (YFV 17D) and alphaviruses (SINV K1487) in human pancreatic adenocarcinoma cell lines AsPC-1, BxPC-3, and Capan-2, which are characterized by high resistance to viral oncolysis.

Materials and methods: Human pancreatic adenocarcinoma cell lines: AsPC-1, BxPC-3, and Capan-2 from the collection of Laboratory of Tick-Borne Encephalitis Chumakov FSC R&D IBP RAS (Institute of Poliomyelitis). Viruses: yellow fever virus strain 17D and Sindbis virus strain K1487 (GenBank AC № PZ244961.1). Virus quantification was performed using the plaque assay on Vero cell culture and real-time PCR.

Results: In this study, we investigated the effect of ruxolitinib (a JAK1/2 kinase inhibitor) on the replicative activity of certain oncolytic flaviviruses (YFV 17D) and alphaviruses (SINV K1487) in virus-resistant human pancreatic adenocarcinoma cell lines AsPC-1, BxPC-3, and Capan-2. A significant dose-dependent increase in infectious titers (by 2-3 orders of magnitude) of YFV 17D and SINV K1487 was demonstrated in the studied cultures in the presence of various concentrations of ruxolitinib (0.1 μM, 0.5 μM, 1.0 μM, and 5.0 μM).

Conclusion: Enhanced replication of oncolytic flaviviruses and alphaviruses in the presence of ruxolitinib could significantly improve the efficacy of therapy for resistant and highly immunosuppressive pancreatic cancer. This combined virotherapy approach can activate powerful immunomediated cell death mechanisms even without an overt cytopathic effect in culture.

ruxolitinib增强抗药人胰腺腺癌细胞系中溶瘤黄病毒和甲病毒的复制。
利用溶瘤病毒克服胰腺癌(PC)的免疫抑制微环境似乎是一种很有前途的治疗方法。然而,肿瘤细胞具有显著的异质性,包括具有高基础JAK/STAT信号活性的耐药细胞群体。克服这种耐药性的一个潜在方法是使用JAK1/2激酶抑制剂,如ruxolitinib,其疗效已经在几项研究中得到证实。目的:研究ruxolitinib(一种JAK1/2激酶抑制剂)对溶瘤黄病毒(YFV 17D)和甲病毒(SINV K1487)在人胰腺腺癌细胞株AsPC-1、BxPC-3和Capan-2中复制活性的影响。材料和方法:人胰腺腺癌细胞系:AsPC-1, BxPC-3和Capan-2,来自Chumakov FSC R&D IBP RAS(小儿麻痹症研究所)蜱传脑炎实验室。病毒:黄热病病毒株17D和Sindbis病毒株K1487 (GenBank AC№PZ244961.1)。采用Vero细胞培养空斑试验和实时PCR进行病毒定量。结果:本研究研究了ruxolitinib(一种JAK1/2激酶抑制剂)对某些溶瘤黄病毒(YFV 17D)和甲病毒(SINV K1487)在病毒抗性人胰腺腺癌细胞系AsPC-1、BxPC-3和Capan-2中复制活性的影响。在不同浓度的ruxolitinib (0.1 μM, 0.5 μM, 1.0 μM和5.0 μM)存在下,YFV 17D和SINV K1487的感染滴度显着呈剂量依赖性增加(2-3个数量级)。结论:鲁索利替尼作用下增强溶瘤黄病毒和甲病毒的复制,可显著提高耐药和高度免疫抑制胰腺癌的治疗效果。这种联合病毒治疗方法可以激活强大的免疫介导的细胞死亡机制,即使在培养中没有明显的细胞病变作用。
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来源期刊
Voprosy virusologii
Voprosy virusologii Medicine-Infectious Diseases
CiteScore
2.00
自引率
0.00%
发文量
48
期刊介绍: The journal deals with advances in virology in Russia and abroad. It publishes papers dealing with investigations of viral diseases of man, animals and plants, the results of experimental research on different problems of general and special virology. The journal publishes materials are which promote introduction into practice of the achievements of the virological science in the eradication and incidence reduction of infectious diseases, as well as their diagnosis, treatment and prevention. The reader will find a description of new methods of investigation, new apparatus and devices.
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