Institute of Immunology and Molecular Medicine, Jining Medical University, Jining 272067, China.
Institute of Basic Medical College, Jining Medical University, Jining 272067, China.
Int J Mol Sci. 2020 Sep 2;21(17):6357. doi: 10.3390/ijms21176357.
Invasive breast cancer is highly regulated by tumor-derived cytokines in tumor microenvironment. The development of drugs that specifically target cytokines are promising in breast cancer treatment. In this study, we reported that arctigenin, a bioactive compound from L., could decrease tumor-promoting cytokines GM-CSF, MMP-3, MMP-9 and TSLP in breast cancer cells. Arctigenin not only inhibited the proliferation, but also the invasion and stemness of breast cancer cells via decreasing GM-CSF and TSLP. Mechanistically, arctigenin decreased the promoter activities of GM-CSF and TSLP via reducing the nuclear translocation of NF-κB p65 which is crucial for the transcription of GM-CSF and TSLP. Furthermore, arctigenin-induced depletion of GM-CSF and TSLP inhibited STAT3 phosphorylation and β-catenin signaling resulting in decreased proliferation, invasion and stemness of breast cancer cells in vitro and in vivo. Our findings provide new insights into the mechanism by which tumor-promoting cytokines regulate breast cancer progression and suggest that arctigenin is a promising candidate for cytokine-targeted breast cancer therapy.
肿瘤微环境中的肿瘤衍生细胞因子高度调控浸润性乳腺癌。特异性靶向细胞因子的药物在乳腺癌治疗中具有广阔的前景。在这项研究中,我们报道了从 L.中提取的生物活性化合物 可降低乳腺癌细胞中促肿瘤细胞因子 GM-CSF、MMP-3、MMP-9 和 TSLP。 不仅通过降低 GM-CSF 和 TSLP 来抑制乳腺癌细胞的增殖,还抑制了其侵袭和干性。从机制上讲, 通过减少 GM-CSF 和 TSLP 转录所必需的 NF-κB p65 的核易位,降低了 GM-CSF 和 TSLP 的启动子活性。此外, 诱导的 GM-CSF 和 TSLP 耗竭抑制了 STAT3 磷酸化和 β-连环蛋白信号通路,导致乳腺癌细胞在体外和体内的增殖、侵袭和干性降低。我们的研究结果为肿瘤促进细胞因子调控乳腺癌进展的机制提供了新的见解,并表明 是细胞因子靶向乳腺癌治疗的有前途的候选药物。