Kurzava Kendall Lucinda, Ma Yuexi, Yang Tony, Lubecka Katarzyna, Stefanska Barbara
Department of Nutritional Sciences, Purdue University, West Lafayette, IN 47907, USA.
Food, Nutrition and Health Program, Faculty of Land and Food Systems, The University of British Columbia, Vancouver, BC V6T 1Z4, Canada.
Nutrients. 2024 Feb 29;16(5):699. doi: 10.3390/nu16050699.
The crosstalk between oncogenic signaling pathways plays a crucial role in driving cancer development. We previously demonstrated that dietary polyphenols, specifically resveratrol (RSV) and other stilbenoids, epigenetically target oncogenes for silencing via DNA hypermethylation in breast cancer. In the present study, we identify signal transduction regulators among RSV-hypermethylated targets and investigate the functional role of RSV-mediated DNA hypermethylation in the regulation of Hedgehog and Wnt signaling. Non-invasive ER-positive MCF-7 and highly invasive triple-negative MCF10CA1a human breast cancer cell lines were used as experimental models. Upon 9-day exposure to 15 µM RSV, pyrosequencing and qRT-PCR were performed to assess DNA methylation and expression of and , which are upstream regulators of the Hedgehog and Wnt pathways, respectively. Our results showed that RSV led to a DNA methylation increase within and enhancers, which was accompanied by decreases in gene expression. Consistently, we observed the downregulation of genes downstream of the Hedgehog and Wnt signaling, including common targets shared by both pathways, and . Further analysis using chromatin immunoprecipitation identified increased H3K27 trimethylation and decreased H3K9 and H3K27 acetylation, along with abolishing OCT1 transcription factor binding. Those changes indicate a transcriptionally silent chromatin state at and enhancers. The inhibition of the Wnt signal transduction was confirmed using a phospho-antibody array that demonstrated suppression of positive and stimulation of negative Wnt regulators. In conclusion, our results provide scientific evidence for dietary polyphenols as epigenetics-modulating agents that act to re-methylate and silence oncogenes, reducing the oncogenic signal transduction. Targeting such an action could be an effective strategy in breast cancer prevention and/or adjuvant therapy.
致癌信号通路之间的相互作用在推动癌症发展中起着关键作用。我们之前证明,膳食多酚,特别是白藜芦醇(RSV)和其他芪类化合物,可通过乳腺癌中的DNA高甲基化在表观遗传上靶向致癌基因使其沉默。在本研究中,我们在RSV高甲基化靶点中鉴定信号转导调节因子,并研究RSV介导的DNA高甲基化在调节Hedgehog和Wnt信号中的功能作用。非侵袭性雌激素受体阳性MCF-7和高侵袭性三阴性MCF10CA1a人乳腺癌细胞系用作实验模型。在15 µM RSV处理9天后,进行焦磷酸测序和qRT-PCR以评估DNA甲基化以及分别作为Hedgehog和Wnt通路上游调节因子的 和 的表达。我们的结果表明,RSV导致 和 增强子内的DNA甲基化增加,同时伴随着基因表达的降低。一致地,我们观察到Hedgehog和Wnt信号下游基因的下调,包括两条通路共有的常见靶点 和 。使用染色质免疫沉淀的进一步分析确定H3K27三甲基化增加,H3K9和H3K27乙酰化减少,同时OCT1转录因子结合消失。这些变化表明 和 增强子处于转录沉默的染色质状态。使用磷酸化抗体阵列证实了Wnt信号转导的抑制,该阵列显示阳性Wnt调节因子受到抑制,阴性Wnt调节因子受到刺激。总之,我们的结果为膳食多酚作为表观遗传调节剂提供了科学证据,这些调节剂可使致癌基因重新甲基化并使其沉默,从而减少致癌信号转导。针对这种作用可能是乳腺癌预防和/或辅助治疗的有效策略。