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The role of flavonoids in the regulation of epithelial‐mesenchymal transition in cancer: A review on targeting signaling pathways and metastasis

上皮-间质转换 转移 生物 细胞生物学 转录因子 小RNA 细胞迁移 细胞生长 信号转导 癌细胞 细胞外基质 癌症研究 细胞 癌症 遗传学 基因
作者
Carina Proença,Marisa Freitas,Daniela Ribeiro,Ana T. Rufino,Eduarda Fernandes,José Miguel P. Ferreira de Oliveira
出处
期刊:Medicinal Research Reviews [Wiley]
卷期号:43 (6): 1878-1945 被引量:18
标识
DOI:10.1002/med.21966
摘要

Abstract One of the hallmarks of cancer is metastasis, a process that entails the spread of cancer cells to distant regions in the body, culminating in tumor formation in secondary organs. Importantly, the proinflammatory environment surrounding cancer cells further contributes to cancer cell transformation and extracellular matrix destruction. During metastasis, front‐rear polarity and emergence of migratory and invasive features are manifestations of epithelial‐mesenchymal transition (EMT). A variety of transcription factors (TFs) are implicated in the execution of EMT, the most prominent belonging to the Snail Family Transcriptional Repressor (SNAI) and Zinc Finger E‐Box Binding Homeobox (ZEB) families of TFs. These TFs are regulated by interaction with specific microRNAs (miRNAs), as miR34 and miR200. Among the several secondary metabolites produced in plants, flavonoids constitute a major group of bioactive molecules, with several described effects including antioxidant, antiinflammatory, antidiabetic, antiobesogenic, and anticancer effects. This review scrutinizes the modulatory role of flavonoids on the activity of SNAI/ZEB TFs and on their regulatory miRNAs, miR‐34, and miR‐200. The modulatory role of flavonoids can attenuate mesenchymal features and stimulate epithelial features, thereby inhibiting and reversing EMT. Moreover, this modulation is concomitant with the attenuation of signaling pathways involved in diverse processes as cell proliferation, cell growth, cell cycle progression, apoptosis inhibition, morphogenesis, cell fate, cell migration, cell polarity, and wound healing. The antimetastatic potential of these versatile compounds is emerging and represents an opportunity for the synthesis of more specific and potent agents.
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