Laboratory for Translational Cancer Research, Department of Biochemistry, Institute of Science, Banaras Hindu University, Varanasi 221005, Uttar Pradesh, India.
Chemical Sciences and Technology Division, CSIR-National Institute for Interdisciplinary Science and Technology, Thiruvananthapuram 695019, Kerala, India.
Biochim Biophys Acta Gen Subj. 2018 Dec;1862(12):2738-2749. doi: 10.1016/j.bbagen.2018.08.016. Epub 2018 Aug 24.
Breast cancer remains one of the leading causes of cancer related deaths in women worldwide. Bharangin is a diterpenoid quinonemethide that has demonstrated therapeutic potential against leukemia, lymphoma, and multiple myeloma cells. Whether this diterpenoid exhibit activities against breast cancer cells and the underlying mechanism is largely unknown. Herein, we provide evidence that bharangin suppresses the proliferation of MCF-7, MDA-MB-231, MDA-MB-453, MDA-MB-468 and T-47D breast cancer cells. As examined by AO/PI staining, DAPI staining, sub-G1 analysis, phosphatidylserine externalization, caspase activation, DNA laddering, and poly-ADP ribose polymerase cleavage, the diterpenoid induced apoptosis in breast cancer cells. The growth inhibitory effect of bharangin on breast cancer cells was further confirmed from colony-formation assay. Furthermore, the cancer cell migration was also suppressed by the diterpenoid. Mechanistically, bharangin was found to modulate multiple cancer related cell signalling pathways in breast cancer cells. Bharangin suppressed the expression of cell survival and invasive proteins, and induced Bax and mitochondrial depolarization in breast cancer cells. The diterpenoid also suppressed the activation of pro-inflammatory transcription factor, nuclear factor (NF)-κB induced by okadaic acid. Finally, the diterpenoid induced the expression of tumor suppressor lncRNAs (MEG-3, GAS-5), while down-regulating oncogenic H19 expression. Overall, these results suggest that bharangin exhibits anti-carcinogenic, anti-proliferative and anti-inflammatory activities against breast cancer cells. The modulation of lncRNA expression and inhibition of NF-κB activation by bharangin may contribute to its anti-carcinogenic activities.
乳腺癌仍然是全球女性癌症相关死亡的主要原因之一。波罗苷是一种二萜醌甲醚,已被证明对白血病、淋巴瘤和多发性骨髓瘤细胞具有治疗潜力。这种二萜是否对乳腺癌细胞具有活性以及其潜在机制在很大程度上尚不清楚。本文提供了证据表明波罗苷可抑制 MCF-7、MDA-MB-231、MDA-MB-453、MDA-MB-468 和 T-47D 乳腺癌细胞的增殖。通过 AO/PI 染色、DAPI 染色、亚 G1 分析、磷脂酰丝氨酸外化、半胱天冬酶激活、DNA 梯状带形成和多聚 ADP 核糖聚合酶切割检测,二萜在乳腺癌细胞中诱导细胞凋亡。通过集落形成实验进一步证实了波罗苷对乳腺癌细胞生长抑制作用。此外,该二萜还抑制了癌细胞的迁移。从机制上讲,波罗苷调节了乳腺癌细胞中的多种癌症相关细胞信号通路。波罗苷抑制了细胞存活和侵袭蛋白的表达,并诱导了乳腺癌细胞中的 Bax 和线粒体去极化。该二萜还抑制了 okadaic 酸诱导的促炎转录因子核因子 (NF)-κB 的激活。最后,该二萜诱导了肿瘤抑制 lncRNA(MEG-3、GAS-5)的表达,同时下调了致癌基因 H19 的表达。综上所述,这些结果表明波罗苷对乳腺癌细胞具有抗癌、抗增殖和抗炎活性。波罗苷对 lncRNA 表达的调节和 NF-κB 激活的抑制可能是其抗癌活性的原因之一。