Danpipat Apisara, Rujimongkon Kitiya, Adchariyasakulchai Patthamapon, Wilawan Nanticha, Ketchart Wannarasmi
Department of Pharmacology, Faculty of Medicine, Chulalongkorn University, 1873 Rama IV Road., Pathumwan, Bangkok, 10330, Thailand.
Medical Science Program, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Jun;398(6):7475-7488. doi: 10.1007/s00210-024-03737-w. Epub 2025 Jan 4.
Zoledronic acid (ZA), a bisphosphonate, is commonly used in breast cancer patients with bone metastases to treat hypercalcemia and osteolysis. Recent studies showed the anti-cancer effects of ZA in breast cancer. This study further explored the synergistic effects of sequential and nonsequential ZA and doxorubicin (DOX) administration on estrogen receptor (ER)-positive and -negative breast cancer cell lines. Anti-cancer and anti-invasion effects were evaluated using MTT and Matrigel invasion assays. The synergistic effects were analyzed using the Chou-Talalay method. The protein levels of invasive and angiogenic factors were assessed by western blot. ZA was found to inhibit the proliferation of ER-positive and -negative breast cancer cells in a concentration-dependent manner. When ZA and doxorubicin (DOX) were sequentially combined at nontoxic concentrations, synergistic effects were observed in sequential administrations with DOX followed by ZA only in ER-negative breast cancer cells. Conversely, the sequential and nonsequential treatments did not significantly differ in ER-positive breast cancer cells. Moreover, this sequential treatment significantly reduced cell invasion and MMP9, pNF-κB, and FGF2 protein levels in ER-negative cells. The results suggest that ZA potentially inhibits ER-negative cells by suppressing the canonical NF-κB pathway and its downstream proteins, MMP9 and FGF2. Furthermore, DOX pretreatment enhanced the ZA effect and increased cell sensitivity to ZA, leading to improved outcomes with lower concentrations and shorter drug exposure durations. When combined with DOX, ZA produced synergistic effects on cell proliferation and invasion when administered sequentially in ER-negative breast cancer cells.
唑来膦酸(ZA)是一种双膦酸盐,常用于患有骨转移的乳腺癌患者,以治疗高钙血症和骨质溶解。最近的研究显示了ZA在乳腺癌中的抗癌作用。本研究进一步探讨了序贯和非序贯给予ZA与多柔比星(DOX)对雌激素受体(ER)阳性和阴性乳腺癌细胞系的协同作用。使用MTT和基质胶侵袭试验评估抗癌和抗侵袭作用。使用Chou-Talalay方法分析协同作用。通过蛋白质免疫印迹法评估侵袭和血管生成因子的蛋白质水平。发现ZA以浓度依赖性方式抑制ER阳性和阴性乳腺癌细胞的增殖。当ZA和多柔比星(DOX)以无毒浓度序贯联合使用时,仅在ER阴性乳腺癌细胞中观察到DOX后序贯给予ZA的序贯给药有协同作用。相反,序贯和非序贯治疗在ER阳性乳腺癌细胞中没有显著差异。此外,这种序贯治疗显著降低了ER阴性细胞中的细胞侵袭以及MMP9、pNF-κB和FGF2蛋白水平。结果表明,ZA可能通过抑制经典NF-κB途径及其下游蛋白MMP9和FGF2来抑制ER阴性细胞。此外,DOX预处理增强了ZA的作用并增加了细胞对ZA的敏感性,从而在较低浓度和较短药物暴露时间下产生更好的结果。当与DOX联合使用时,ZA在ER阴性乳腺癌细胞中序贯给药时对细胞增殖和侵袭产生协同作用。