Department of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah, Saudi Arabia.
Int J Nanomedicine. 2021 Dec 16;16:8159-8184. doi: 10.2147/IJN.S338272. eCollection 2021.
Conventional therapies for cancer eradication like surgery, radiotherapy, and chemotherapy, even though most widely used, still suffer from some disappointing outcomes. The limitations of these therapies during cancer recurrence and metastasis demonstrate the need for better alternatives. Some bacteria preferentially colonize and proliferate inside tumor mass; thus these bacteria can be used as ideal candidates to deliver antitumor therapeutic agents. The bacteria like spp., spp., spp., and spp. can be reprogrammed to produce, transport, and deliver anticancer agents, eg, cytotoxic agents, prodrug converting enzymes, immunomodulators, tumor stroma targeting agents, siRNA, and drug-loaded nanoformulations based on clinical requirements. In addition, these bacteria can be genetically modified to express various functional proteins and targeting ligands that can enhance the targeting approach and controlled drug-delivery. Low tumor-targeting and weak penetration power deep inside the tumor mass limits the use of anticancer drug-nanoformulations. By using anticancer drug nanoformulations and other therapeutic payloads in combination with antitumor bacteria, it makes a synergistic effect against cancer by overcoming the individual limitations. The tumor-targeting bacteria can be either used as a monotherapy or in addition with other anticancer therapies like photothermal therapy, photodynamic therapy, and magnetic field therapy to accomplish better clinical outcomes. The toxicity issues on normal tissues is the main concern regarding the use of engineered antitumor bacteria, which requires deeper research. In this article, the mechanism by which bacteria sense tumor microenvironment, role of some anticancer agents, and the recent advancement of engineering bacteria with different therapeutic payloads to combat cancers has been reviewed. In addition, future prospective and some clinical trials are also discussed.
尽管手术、放疗和化疗等传统癌症治疗方法被广泛应用,但仍存在一些不尽如人意的结果。这些疗法在癌症复发和转移时的局限性表明需要更好的替代方法。有些细菌优先在肿瘤块内定植和增殖;因此,这些细菌可以作为理想的候选物来输送抗肿瘤治疗剂。像 spp.、 spp.、 spp. 和 spp. 等细菌可以被重新编程以产生、运输和输送抗肿瘤药物,例如细胞毒性药物、前药转化酶、免疫调节剂、肿瘤基质靶向剂、siRNA 和基于临床需求的载药纳米制剂。此外,这些细菌可以进行基因修饰以表达各种功能蛋白和靶向配体,从而增强靶向方法和控制药物递送。抗癌药物纳米制剂的低肿瘤靶向性和在肿瘤块内深部的弱穿透能力限制了其应用。通过将抗癌药物纳米制剂和其他治疗有效载荷与抗肿瘤细菌联合使用,可以通过克服个体局限性来产生对抗癌症的协同作用。肿瘤靶向细菌可以单独使用或与其他抗癌疗法(如光热疗法、光动力疗法和磁场疗法)联合使用,以实现更好的临床效果。在使用工程抗肿瘤细菌时,对正常组织的毒性问题是主要关注点,这需要进一步研究。本文综述了细菌感知肿瘤微环境的机制、一些抗肿瘤药物的作用,以及利用不同治疗有效载荷工程化细菌来对抗癌症的最新进展。此外,还讨论了未来的前景和一些临床试验。