Eisenstark Abraham, Kazmierczak Robert A, Dino Alison, Khreis Rula, Newman Dustin, Schatten Heide
Cancer Research Center and Division of Biological Sciences, University of Missouri, Columbia, USA.
Methods Mol Biol. 2007;394:323-54. doi: 10.1007/978-1-59745-512-1_16.
Despite significant progress in the development of new drugs and radiation, deaths due to cancer remain high. Many novel therapies are in clinical trials and offer better solutions, but more innovative approaches are needed to eradicate the various subpopulations that exist in solid tumors. Since 1997, the use of bacteria for cancer therapy has gained increased attention. Salmonella Typhimurium strains have been shown to have a remarkably high affinity for tumor cells. The use of bacterial strains to target tumors is a relatively new research method that has not yet reached the point of clinical success. The first step in assessing the effectiveness of bacterial tumor therapy will require strain development and preclinical comparisons of candidate strains, which is the focus of this chapter. Several investigators have developed strains of Salmonella with reduced toxicity and capacity to deliver anti-tumor agents. Although methods for obtaining safe therapeutic strains have been relatively successful, there is still need for further genetic engineering before successful clinical use in human patients. As described by Forbes et al. in 2003, the main stumbling block is that, while bacteria preferentially embed within tumor cells, they fail to spread within the tumor and finish the eradication process. Further engineering might focus on creating Salmonella that remove motility limitations, including increased affinity toward tumor-generated chemotactic attractants and induction of matrix-degrading enzymes.
尽管在新药研发和放疗方面取得了显著进展,但癌症导致的死亡人数仍然居高不下。许多新型疗法正在进行临床试验并提供了更好的解决方案,但仍需要更多创新方法来根除实体瘤中存在的各种亚群。自1997年以来,利用细菌进行癌症治疗越来越受到关注。鼠伤寒沙门氏菌菌株已被证明对肿瘤细胞具有极高的亲和力。利用细菌菌株靶向肿瘤是一种相对较新的研究方法,尚未达到临床成功的阶段。评估细菌肿瘤治疗效果的第一步需要进行菌株开发和候选菌株的临床前比较,这是本章的重点。几位研究人员已经开发出了毒性降低且能够递送抗肿瘤药物的沙门氏菌菌株。尽管获得安全治疗菌株的方法相对成功,但在成功用于人类患者的临床治疗之前,仍需要进一步的基因工程。正如福布斯等人在2003年所描述的,主要障碍在于,虽然细菌优先嵌入肿瘤细胞内,但它们无法在肿瘤内扩散并完成根除过程。进一步的工程改造可能集中在创造出能够消除运动限制的沙门氏菌,包括增强对肿瘤产生的趋化吸引剂的亲和力以及诱导基质降解酶。