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CERTAIN IMPROVED COMBINATION BACTERIOLYTIC THERAPY FOR THE TREATMENT OF TUMORS

机译:某些改良的联合细菌疗法治疗肿瘤

摘要

Current approaches for treating cancer are limited, in part, by the inability of drugs to affect the poorly vascularized regions of tumors. We have found that spores of anaerobic bacteria in combination with agents which interact with microtubules can cause the destruction of both the vascular and avascular compartments of tumors. Two classes of microtubule inhibitors were found to exert markedly different effects. Some agents that inhibited microtubule synthesis such as HTI-286 and vinorelbine, caused rapid, massive hemorrhagic necrosis when used in combination with spores. In contrast, agents that stabilized microtubules, such as the taxanes docetaxel and MAC-321, resulted in slow tumor regressions that killed most neoplastic cells. Remaining cells in the poorly perfused regions of tumors could be eradicated by sporulated bacteria Mechanistic studies showed that the microtubule destabilizers, but not the microtubule stabilizers, radically reduced blood flow to tumors, thereby enlarging the hypoxic niche in which spores could germinate. A single intravenous injection of spores plus selected microtubule-interacting agents was able to cause regressions of several tumors in the absence of excessive toxicity.
机译:当前用于治疗癌症的方法在一定程度上受到药物无法影响肿瘤血管较弱的区域的限制。我们已经发现,厌氧细菌的孢子与与微管相互作用的试剂结合可以破坏肿瘤的血管和无血管腔室。发现两类微管抑制剂发挥明显不同的作用。当与孢子结合使用时,某些抑制微管合成的药物,例如HTI-286和长春瑞滨,会导致快速,大量的出血性坏死。相比之下,紫杉烷类紫杉萜和MAC-321等稳定微管的药物可导致缓慢的肿瘤消退,从而杀死大多数肿瘤细胞。形成孢子的细菌可以根除肿瘤灌注不良区域中的剩余细胞。机理研究表明,微管去稳定剂而不是微管稳定剂从根本上减少了流向肿瘤的血流量,从而扩大了芽孢可能萌发的低氧环境。在没有过度毒性的情况下,单次静脉内注射孢子加选定的微管相互作用剂能够导致几种肿瘤消退。

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