Zhang Hong, Zhu Tao, Fu Ruoqiu, Peng Yang, Jing Peng, Xu Wenchun, Wang Hong, Li Sijie, Shu Zhaoche, Yin Yibing, Zhang Xuemei
Department of Laboratory Medicine, Key Laboratory of Diagnostic Medicine (Ministry of Education), Chongqing Medical University, Chongqing 400016, China.
Department of Laboratory Medicine, The Affiliated Hospital of North Sichuan Medical College and Department of Laboratory Medicine and Translational Medicine Research Center, North Sichuan Medical College, Nanchong 637000, China.
Mol Ther Oncolytics. 2020 Jun 24;18:247-261. doi: 10.1016/j.omto.2020.06.015. eCollection 2020 Sep 25.
Increasing evidence demonstrates that microorganisms and their products can modulate host responses to cancer therapies and contribute to tumor shrinkage via various mechanisms, including intracellular signaling pathways modulation and immunomodulation. Detoxified pneumolysin derivative ΔA146Ply is a pneumolysin mutant lacking hemolytic activity. To determine the antitumor activity of ΔA146Ply, the combination of ΔA146Ply and berbamine, a well-established antitumor agent, was used for breast cancer therapy, especially for triple-negative breast cancer. The efficacy of the combination therapy was evaluated using four breast cancer cell lines and using a synergistic mouse tumor model. We demonstrated that , the combination therapy significantly inhibited cancer cell proliferation, promoted cancer cell apoptosis, caused cancer cell-cycle arrest, and suppressed cancer cell migration and invasion. , the combination therapy significantly suppressed tumor growth and prolonged the median survival time of tumor-bearing mice partially through inhibiting tumor cell proliferation, promoting tumor cell apoptosis, and activating systemic antitumor immune responses. The safety analysis demonstrated that the combination therapy showed no obvious liver and kidney toxicity to tumor-bearing mice. Our study provides a new treatment option for breast cancer and lays the experimental basis for the development of ΔA146Ply as an antitumor agent.
越来越多的证据表明,微生物及其产物可以调节宿主对癌症治疗的反应,并通过多种机制促进肿瘤缩小,包括调节细胞内信号通路和免疫调节。解毒的肺炎球菌溶血素衍生物ΔA146Ply是一种缺乏溶血活性的肺炎球菌溶血素突变体。为了确定ΔA146Ply的抗肿瘤活性,将ΔA146Ply与一种成熟的抗肿瘤药物小檗胺联合用于乳腺癌治疗,尤其是三阴性乳腺癌。使用四种乳腺癌细胞系和一种协同小鼠肿瘤模型评估联合治疗的疗效。我们证明,联合治疗显著抑制癌细胞增殖,促进癌细胞凋亡,导致癌细胞周期停滞,并抑制癌细胞迁移和侵袭。此外,联合治疗显著抑制肿瘤生长,部分通过抑制肿瘤细胞增殖、促进肿瘤细胞凋亡和激活全身抗肿瘤免疫反应,延长荷瘤小鼠的中位生存时间。安全性分析表明,联合治疗对荷瘤小鼠没有明显的肝肾毒性。我们的研究为乳腺癌提供了一种新的治疗选择,并为开发ΔA146Ply作为抗肿瘤药物奠定了实验基础。