Mascheroni Pietro, Meyer-Hermann Michael, Hatzikirou Haralampos
Braunschweig Integrated Centre of Systems Biology and Helmholtz Centre for Infection Research, Braunschweig, Germany.
Centre for Individualized Infection Medicine, Hannover, Germany.
Front Microbiol. 2020 Jun 4;11:1083. doi: 10.3389/fmicb.2020.01083. eCollection 2020.
Tumor-targeting bacteria elicit anticancer effects by infiltrating hypoxic regions, releasing toxic agents and inducing immune responses. Although current research has largely focused on the influence of chemical and immunological aspects on the mechanisms of bacterial therapy, the impact of physical effects is still elusive. Here, we propose a mathematical model for the anti-tumor activity of bacteria in avascular tumors that takes into account the relevant chemo-mechanical effects. We consider a time-dependent administration of bacteria and analyze the impact of bacterial chemotaxis and killing rate. We show that active bacterial migration toward tumor hypoxic regions provides optimal infiltration and that high killing rates combined with high chemotactic values provide the smallest tumor volumes at the end of the treatment. We highlight the emergence of steady states in which a small population of bacteria is able to constrain tumor growth. Finally, we show that bacteria treatment works best in the case of tumors with high cellular proliferation and low oxygen consumption.
肿瘤靶向细菌通过浸润缺氧区域、释放毒性因子和诱导免疫反应来引发抗癌作用。尽管目前的研究主要集中在化学和免疫学方面对细菌治疗机制的影响,但物理效应的影响仍然难以捉摸。在此,我们提出了一个针对无血管肿瘤中细菌抗肿瘤活性的数学模型,该模型考虑了相关的化学-力学效应。我们考虑了细菌的时间依赖性给药,并分析了细菌趋化性和杀伤率的影响。我们表明,细菌向肿瘤缺氧区域的主动迁移可实现最佳浸润,并且高杀伤率与高趋化值相结合可在治疗结束时使肿瘤体积最小。我们强调了稳态的出现,即少量细菌能够抑制肿瘤生长。最后,我们表明细菌治疗在细胞增殖高且耗氧量低的肿瘤中效果最佳。