State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, China.
Phytomedicine. 2021 May;85:153551. doi: 10.1016/j.phymed.2021.153551. Epub 2021 Mar 18.
Triple-negative breast cancer (TNBC), lacking targeted therapies currently, is susceptible to ferroptosis, a recently defined form of cell death.
To evaluate the anticancer activity of Shuganning injection (SGNI), a traditional Chinese patent medicine, on TNBC cells; To elucidate the mechanism of SGNI induced ferroptosis.
The anticancer activity of SGNI was examined via in vitro cell proliferation assays and in vivo xenograft growth assay. Ferroptosis was determined by flow-cytometric analysis of lipid ROS, labile iron pool measurement, and propidium iodide exclusion assay. The dependency on heme oxygenase 1 (HO-1) of SGNI induced ferroptosis was confirmed by genetic knockdown and pharmacological inhibition of the protein.
SGNI selectively inhibited the proliferation of TNBC cells compared to non-TNBC breast cancer cells and normal cells. The cell death induced by SGNI in TNBC cells showed distinct morphology from apoptosis and could not be rescued by the pan-caspase inhibitor Z-VAD(OMe)-FMK. On the other hand, SGNI induced cell death was blocked by the lipid ROS scavengers ferrostatin-1 and liproxstatin-1, the acyl-CoA synthetase long chain family member 4 inhibitor rosiglitazone, and the iron chelators 1,10-phenanthroline and deferoxamine. These data indicated that SGNI induced a ferroptotic cell death of TNBC cells. Mechanistically, SGNI induced ferroptosis was dependent on HO-1, which promotes intracellular labile iron pool accumulation, and was alleviated by HO-1 knockdown and inhibition by tin protoporphyrin IX. In line with the in vitro data, SGNI significantly inhibited the xenograft growth of TNBC cell line MD-MB-231 in nude mice.
Collectively, our study elaborates on a promising regimen for TNBC treatment through induction of ferroptosis by SGNI, a traditional Chinese patent medicine currently available in the clinic, which merits further investigation.
三阴性乳腺癌(TNBC)目前缺乏靶向治疗药物,易发生铁死亡,这是一种新定义的细胞死亡形式。
评估中药舒肝宁注射液(SGNI)对 TNBC 细胞的抗癌活性;阐明 SGNI 诱导铁死亡的机制。
通过体外细胞增殖试验和体内异种移植生长试验检测 SGNI 的抗癌活性。通过流式细胞术分析脂质 ROS、不稳定铁池测量和碘化丙啶排除试验来确定铁死亡。通过基因敲低和蛋白药理学抑制来确认 SGNI 诱导的铁死亡对血红素加氧酶 1(HO-1)的依赖性。
SGNI 选择性抑制 TNBC 细胞的增殖,而对非 TNBC 乳腺癌细胞和正常细胞的增殖没有影响。SGNI 诱导的 TNBC 细胞死亡与细胞凋亡的形态不同,不能被泛半胱天冬酶抑制剂 Z-VAD(OMe)-FMK 挽救。另一方面,SGNI 诱导的细胞死亡被脂质 ROS 清除剂 ferrostatin-1 和 liproxstatin-1、酰基辅酶 A 合成酶长链家族成员 4 抑制剂罗格列酮和铁螯合剂 1,10-邻菲啰啉和去铁胺阻断。这些数据表明,SGNI 诱导 TNBC 细胞发生铁死亡。在机制上,SGNI 诱导的铁死亡依赖于 HO-1,它促进细胞内不稳定铁池的积累,HO-1 敲低和锡原卟啉 IX 抑制可减轻这种积累。与体外数据一致,SGNI 显著抑制了裸鼠中 TNBC 细胞系 MD-MB-231 的异种移植生长。
总之,我们的研究通过 SGNI(一种目前临床上可用的中药)诱导铁死亡,阐述了一种治疗 TNBC 的有前途的方案,值得进一步研究。