Departments of Biomedical Sciences, College of Medicine, Korea University, 73 Inchon-ro, Seongbuk-gu, Seoul, 136-705, Republic of Korea.
Departments of and Neuroscience, College of Medicine, Korea University, 73 Inchon-ro, Seongbuk-gu, Seoul, 136-705, Republic of Korea.
Sci Rep. 2019 Apr 29;9(1):6595. doi: 10.1038/s41598-019-41224-y.
Breast cancer exhibits high lethality in women because it is frequently detected at an advanced stage and aggressive forms such as triple-negative breast cancer (TNBC), which are often characterized by metastasis through colonization of secondary tumors. Thus, developing therapeutic agents that target the metastatic process is crucial to successfully treat aggressive breast cancer. We evaluated SP-8356, an anti-inflammatory synthetic verbenone derivative, with respect to its regulation of breast cancer cell behavior and cancer progression. Treatment of SP-8356 arrested cell cycle and reduced growth in various types of breast cancer cells with mild cytotoxicity. Particularly, SP-8356 significantly reduced the motility and invasiveness of TNBC cells. Assays using an in vivo xenograft mouse model confirmed the cell-specific anti-proliferative and anti-metastatic activity of SP-8356. Functional studies revealed that SP-8356 suppressed serum response element-dependent reporter gene expression and NF-κB-related signaling, resulting in downregulation of many genes related to cancer invasion. We conclude that SP-8356 suppresses breast cancer progression through multimodal functions, including inhibition of NF-κB signaling and growth-related signaling pathways.
乳腺癌在女性中具有很高的致死率,因为它经常在晚期被发现,而且像三阴性乳腺癌(TNBC)这样的侵袭性形式,通常以通过继发性肿瘤的定植进行转移为特征。因此,开发针对转移过程的治疗剂对于成功治疗侵袭性乳腺癌至关重要。我们评估了 SP-8356,一种抗炎合成马鞭草酮衍生物,以评估其对乳腺癌细胞行为和癌症进展的调节作用。SP-8356 的治疗作用可阻止细胞周期并降低各种类型乳腺癌细胞的生长,其细胞毒性较小。特别是,SP-8356 显著降低了 TNBC 细胞的迁移和侵袭能力。使用体内异种移植小鼠模型的测定证实了 SP-8356 的细胞特异性抗增殖和抗转移活性。功能研究表明,SP-8356 通过抑制血清反应元件依赖性报告基因表达和 NF-κB 相关信号通路来抑制 NF-κB 信号和与生长相关的信号通路,从而下调许多与癌症侵袭相关的基因。我们得出结论,SP-8356 通过多种功能抑制乳腺癌的进展,包括抑制 NF-κB 信号和与生长相关的信号通路。