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DN604-吉西他滨联合治疗对人膀胱癌模型的抗肿瘤作用和细胞迁移抑制作用。

Anti-tumor effects and cell motility inhibition of the DN604-gemcitabine combined treatment in human bladder cancer models.

机构信息

Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China.

Pharmaceutical Research Center and School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China; Jiangsu Province Hi-Tech Key Laboratory for Biomedical Research, Southeast University, Nanjing 211189, China.

出版信息

Bioorg Med Chem. 2021 Jan 1;29:115858. doi: 10.1016/j.bmc.2020.115858. Epub 2020 Nov 7.

Abstract

Bladder cancer is one of the major tumors for men in the world, in which therapy the combination of cisplatin and gemcitabine is still fist-line applied to treat with advanced or metastatic bladder cancer. In our early study, we developed a potential Pt(II) agent, DN604, which has anti-tumor effect as potent as cisplatin toward bladder cancers. Herein, we aim at investigating the combinatory application of DN604 with gemcitabine for bladder cancer treatment. In vitro studies proved that the combined treatment of DN604 and gemcitabine could limit cell proliferation by elevating the incidence of DNA damage induced apoptosis. Notably, further researches showed that the DN604-gemcitabine treatment suppressed cell autophagy to inhibit cell motility upon the ROS dependent p38 MAPK signaling pathway, explicating its better anti-tumor activity than single drug treatment or the cisplatin-gemcitabine treatment. In vivo tests confirmed that the DN604-gemcitabine treatment has superior anti-tumor activity with low toxicity to cisplatin or its combination with gemcitabine treatments. DN604 plus gemcitabine, is of great significance for the treatment with human bladder cancer. Our study has provided a potential combination treatment option.

摘要

膀胱癌是世界上男性的主要肿瘤之一,其中顺铂和吉西他滨的联合治疗仍然是治疗晚期或转移性膀胱癌的一线治疗方法。在我们的早期研究中,我们开发了一种潜在的 Pt(II) 药物 DN604,它对膀胱癌具有与顺铂相当的抗肿瘤作用。在此,我们旨在研究 DN604 与吉西他滨联合治疗膀胱癌的应用。体外研究证明,DN604 和吉西他滨的联合治疗通过提高 DNA 损伤诱导的细胞凋亡的发生率来限制细胞增殖。值得注意的是,进一步的研究表明,DN604-吉西他滨治疗通过 ROS 依赖的 p38 MAPK 信号通路抑制细胞自噬来抑制细胞迁移,其抗肿瘤活性优于单药治疗或顺铂-吉西他滨治疗。体内试验证实,DN604-吉西他滨治疗具有比顺铂或其与吉西他滨联合治疗更低的毒性的优越抗肿瘤活性。DN604 加吉西他滨对人膀胱癌的治疗具有重要意义。我们的研究为联合治疗提供了一种潜在的选择。

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