Jeon Min Seo, Hong Ju-Mi, Kim Jaewon, Kim Jina, Kim Sojin, Sohn Jae Hak, Han Se Jong, Yim Joung Han, Kim Il-Chan
Division of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Republic of Korea.
Department of Biomedical Laboratory Science, Daegu Health College, Daegu 41453, Republic of Korea.
J Microbiol Biotechnol. 2025 Sep 16;35:e2505003. doi: 10.4014/jmb.2505.05003.
SF7354 was isolated from the extremophilic plant collected in Chilean Patagonia and investigated for its anticancer potential. Crude extracts of SF7354 exhibited significant cytotoxic activity against multiple human cancer cell lines, with the most pronounced effect observed in HCT116 cells. Flow cytometry analysis revealed that treatment with the extract induced time-dependent apoptosis and sub-G1 accumulation, indicating activation of programmed cell death. Cell cycle analysis further showed early G0/G1 arrest, followed by a progressive increase in apoptotic populations. Western blot analysis demonstrated notable alterations in PARP and p53 protein levels, suggesting a p53-dependent mechanism of apoptosis. HPLC-based purification of the extract led to the isolation of five benzomalvin derivatives (A-E), all of which exhibited dose- and time-dependent cytotoxicity. These findings suggest that SF7354-derived benzomalvins act through apoptosis-associated mechanisms and represent promising candidates for the development of novel anticancer agents.
SF7354是从采集于智利巴塔哥尼亚的嗜极端植物中分离得到的,并对其抗癌潜力进行了研究。SF7354的粗提物对多种人类癌细胞系表现出显著的细胞毒性活性,其中在HCT116细胞中观察到的效果最为明显。流式细胞术分析显示,提取物处理诱导了时间依赖性的细胞凋亡和亚G1期积累,表明程序性细胞死亡被激活。细胞周期分析进一步显示早期G0/G1期阻滞,随后凋亡细胞群体逐渐增加。蛋白质印迹分析表明PARP和p53蛋白水平有显著变化,提示存在p53依赖性细胞凋亡机制。基于高效液相色谱的提取物纯化导致分离出五种苯并马尔文衍生物(A - E),所有这些衍生物均表现出剂量和时间依赖性的细胞毒性。这些发现表明,源自SF7354的苯并马尔文通过与细胞凋亡相关的机制发挥作用,是开发新型抗癌药物的有前途的候选物。