Department of Pathology, University of Illinois at Chicago, College of Medicine, Chicago, Illinois, USA
Department of Pathology, University of Illinois at Chicago, College of Medicine, Chicago, Illinois, USA.
J Virol. 2018 Sep 12;92(19). doi: 10.1128/JVI.00700-18. Print 2018 Oct 1.
Herpes simplex virus 1 (HSV-1)-mediated oncolytic therapy is an emerging cancer treatment modality with potential effectiveness against a variety of malignancies. To better understand the interaction of HSV-1 with neoplastic cells, we inoculated three-dimensional (3D) cultures of human uveal melanoma cells with HSV-1. 3D melanoma cultures were established by placing tumor cells on the surface of a Matrigel matrix, which was followed by the growth of tumor cells on the matrix surface and invasion of the Matrigel matrix by some tumor cells to form multicellular tumor spheroids within the matrix. When established 3D melanoma cultures were inoculated with HSV-1 by placing virus on the surface of cultures, virus infection caused extensive death of melanoma cells growing on the surface of the 3D matrix and significantly decreased the number of tumor cell spheroids within the matrix. However, HSV-1 infection did not lead to a complete destruction of tumor cells in the 3D cultures during a 17-day observation period and, surprisingly, HSV-1 infection promoted the growth of some melanoma cells within the matrix as determined by the significantly increased size of residual viable multicellular tumor spheroids in virus-inoculated 3D cultures at 17 days after virus inoculation. Acyclovir treatment inhibited HSV-1-induced tumor cell killing but did not block the virus infection-induced increase in spheroid size. These findings suggest that although HSV-1 oncolytic virotherapy may cause extensive tumor cell killing, it may also be associated with the unintended promotion of the growth of some tumor cells. Cancer cells are exposed to HSV-1 during oncolytic virotherapy with the intention of killing tumor cells. Our observations reported here suggest that potential dangers of HSV-1 oncolytic therapy include promotion of growth of some tumor cells. Furthermore, our findings raise the possibility that HSV-1 infection of neoplastic cells during natural infections or vaccinations may promote the growth of tumors. Our study indicates that HSV-1 infection of 3D tumor cell cultures provides an experimental platform in which mechanisms of HSV-1-mediated promotion of tumor cell growth can be effectively studied.
单纯疱疹病毒 1(HSV-1)介导的溶瘤治疗是一种新兴的癌症治疗方式,对多种恶性肿瘤具有潜在的疗效。为了更好地了解 HSV-1 与肿瘤细胞的相互作用,我们将 HSV-1 接种到三维(3D)培养的人眼葡萄膜黑色素瘤细胞中。3D 黑色素瘤培养是通过将肿瘤细胞接种到 Matrigel 基质表面上建立的,随后肿瘤细胞在基质表面上生长,并使一些肿瘤细胞侵入 Matrigel 基质,在基质内形成多细胞肿瘤球体。当建立的 3D 黑色素瘤培养物被接种 HSV-1 时,将病毒放在培养物的表面上,病毒感染导致大量生长在 3D 基质表面上的黑色素瘤细胞死亡,并显著减少了基质内肿瘤细胞球体的数量。然而,在 17 天的观察期内,HSV-1 感染并没有导致 3D 培养物中的肿瘤细胞完全破坏,令人惊讶的是,HSV-1 感染促进了基质内一些黑色素瘤细胞的生长,这可以通过接种病毒后 17 天病毒接种的 3D 培养物中残留的有活力的多细胞肿瘤球体的显著增大来确定。阿昔洛韦治疗抑制 HSV-1 诱导的肿瘤细胞杀伤,但不能阻止病毒感染诱导的球体大小增加。这些发现表明,尽管 HSV-1 溶瘤病毒治疗可能导致广泛的肿瘤细胞杀伤,但它也可能与肿瘤细胞生长的意外促进有关。癌细胞在溶瘤病毒治疗中暴露于 HSV-1 是为了杀死肿瘤细胞。我们在这里报告的观察结果表明,HSV-1 溶瘤治疗的潜在危险包括促进一些肿瘤细胞的生长。此外,我们的研究结果提出了一种可能性,即 HSV-1 感染肿瘤细胞在自然感染或接种疫苗期间可能会促进肿瘤的生长。我们的研究表明,HSV-1 感染 3D 肿瘤细胞培养物提供了一个实验平台,可以有效地研究 HSV-1 介导的促进肿瘤细胞生长的机制。