Jones Travis H, Song Jonathan W, Abushahin Laith
Department of Mechanical and Aerospace Engineering, The Ohio State University, 201W. 19th Avenue, E406 Scott Laboratory, Columbus, OH 43210, United States; Department of Internal Medicine, Division of Medical Oncology, The Ohio State University, 1800 Canon Drive, 1300G, Columbus, OH 43210, United States.
Department of Mechanical and Aerospace Engineering, The Ohio State University, 201W. 19th Avenue, E406 Scott Laboratory, Columbus, OH 43210, United States; Arthur G. James Comprehensive Cancer Center and Richard J. Solove Research Institute, The Ohio State University Medical Center, Columbus, OH 43210, United States.
Transl Oncol. 2022 Jan;15(1):101296. doi: 10.1016/j.tranon.2021.101296. Epub 2021 Nov 27.
Tumor treating fields (TTFields)-an intermediate-frequency, electric field therapy-has emerged as a promising alternative therapy for the treatment of solid cancers. Since the first publication describing the anticancer effects of TTFields in 2004 there have been numerous follow-up studies by other groups, either to confirm the efficacy of TTFields or to study the primary mechanism of interaction. The overwhelming conclusion from these in vitro studies is that TTFields reduce the viability of aggressively replicating cell lines. However, there is still speculation as to the primary mechanism for this effect; moreover, observations both in vitro and in vivo of inhibited migration and metastases have been made, which may be unrelated to the originally proposed hypothesis of replication stress. Adding to this, the in vivo environment is much more complex spatially, structurally, and involves intricate networks of cell signaling, all of which could change the efficacy of TTFields in the same way pharmaceutical interventions often struggle transitioning in vivo. Despite this, TTFields have shown promise in clinical practice on multiple cancer types, which begs the question: has the primary mechanism carried over from in vitro to in vivo or are there new mechanisms at play? The goal of this review is to highlight the current proposed mechanism of action of TTFields based primarily on in vitro experiments and animal models, provide a summary of the clinical efficacy of TTFields, and finally, propose future directions of research to identify all possible mechanisms in vivo utilizing novel tumor-on-a-chip platforms.
肿瘤治疗电场(TTFields)——一种中频电场疗法——已成为治疗实体癌的一种有前景的替代疗法。自2004年首次发表描述TTFields抗癌作用的文章以来,其他研究团队进行了大量后续研究,以确认TTFields的疗效或研究其主要相互作用机制。这些体外研究得出的压倒性结论是,TTFields降低了快速增殖细胞系的活力。然而,对于这种效应的主要机制仍存在推测;此外,在体外和体内都观察到了迁移和转移受到抑制的情况,这可能与最初提出的复制应激假说无关。此外,体内环境在空间和结构上要复杂得多,并且涉及复杂的细胞信号网络,所有这些都可能以与药物干预在体内往往难以转化相同的方式改变TTFields的疗效。尽管如此,TTFields在多种癌症类型的临床实践中已显示出前景,这就引出了一个问题:主要机制是从体外延续到体内的,还是有新的机制在起作用?本综述的目的是主要基于体外实验和动物模型,突出当前提出的TTFields作用机制,总结TTFields的临床疗效,最后提出未来的研究方向,以利用新型芯片上肿瘤平台确定体内所有可能的机制。