Department of Biotechnology, College of Applied Life Science, Jeju National University, Jeju, Korea.
Subtropical/Tropical Organism Gene Bank, Jeju National University, Jeju, Korea.
Mol Carcinog. 2018 Nov;57(11):1467-1479. doi: 10.1002/mc.22870. Epub 2018 Jul 18.
Cancer stem cells (CSCs) as a subpopulation of cancer cells are drug-resistant and radiation-resistant cancer cells to be responsible for tumor progress, maintenance and recurrence of cancer, and metastasis. This study isolated and investigated a new cancer stem cell (CSC) inhibitor derived from lactic acid fermentation products using culture broth with 2% aronia juice. The anti-CSC activity of aronia-cultured broth was significantly higher than that of the control. Activity-guided fractionation and repeated chromatographic preparation led to the isolation of one compound. Using nuclear magnetic resonance and ESI mass spectrometry, we identified the isolated compound as catechol. In this study, we report that aronia-fermented catechol has a novel inhibitory effect on human breast CSCs. Catechol inhibited breast cancer cell proliferation and mammosphere formation in a dose-dependent manner. This compound reduced the CD44 /CD24 subpopulation, ALDH-expressing cell population and the self-renewal-related genes nanog, sox2, and oct4. Catechol preferentially reduced mRNA transcripts and protein levels of Stat3 and did not induce c-Myc degradation. These findings support the novel utilization of catechol for breast cancer therapy via the Stat3/IL-6 signaling pathway. Our results suggest that catechol can be used for breast cancer therapy and that Stat3 expression is a marker of CSCs. Catechol inhibited Stat3 signaling by reducing Stat3 expression and secreted IL-6, a CSC survival factor. These findings support the novel utilization of catechol for breast cancer therapy via Stat3/IL-6 signaling.
癌症干细胞(CSCs)作为癌细胞的一个亚群,是导致肿瘤进展、维持和复发以及转移的耐药和辐射耐药癌细胞。本研究使用含有 2%黑树莓汁的培养液分离并研究了一种源自乳酸发酵产物的新型癌症干细胞(CSC)抑制剂。黑树莓培养物的抗 CSC 活性明显高于对照组。基于活性的分步分离和重复色谱制备导致一种化合物的分离。通过核磁共振和 ESI 质谱,我们鉴定出分离出的化合物为儿茶酚。在这项研究中,我们报告了黑树莓发酵儿茶酚对人乳腺癌 CSCs 具有新颖的抑制作用。儿茶酚以剂量依赖的方式抑制乳腺癌细胞增殖和类器官形成。该化合物降低了 CD44/CD24 亚群、ALDH 表达细胞群以及自我更新相关基因 nanog、sox2 和 oct4。儿茶酚优先降低 Stat3 的 mRNA 转录本和蛋白水平,而不诱导 c-Myc 降解。这些发现支持儿茶酚通过 Stat3/IL-6 信号通路用于乳腺癌治疗的新用途。我们的研究结果表明,儿茶酚可用于乳腺癌治疗,Stat3 表达是 CSCs 的标志物。儿茶酚通过降低 Stat3 表达和分泌 CSC 存活因子 IL-6 来抑制 Stat3 信号。这些发现支持儿茶酚通过 Stat3/IL-6 信号通路用于乳腺癌治疗的新用途。