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Parthenolide inhibits transforming growth factor β1-induced epithelial-mesenchymal transition in colorectal cancer cells

机译:车前草内酯抑制大肠癌细胞转化生长因子β1诱导的上皮-间质转化

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Background/Aims Transforming growth factor-β1 (TGF-β1) induction of epithelial-mesenchymal transition (EMT) is one of the mechanisms by which colorectal cancer (CRC) cells acquire migratory and invasive capacities, and subsequently metastasize. Parthenolide (PT) expresses multiple anti-cancer and anti-inflammatory activities that inhibit nuclear factor κB by targeting the IκB kinase complex. In the present study, we aimed to investigate whether PT can inhibit TGF-β1-induced EMT in CRC cell lines.
机译:背景/目的转化生长因子-β1(TGF-β1)诱导的上皮-间质转化(EMT)是结直肠癌(CRC)细胞获得迁移和侵袭能力并随后转移的机制之一。 Parthenolide(PT)通过靶向IκB激酶复合物表达多种抑制核因子κB的抗癌和抗炎活性。在本研究中,我们旨在研究PT是否可以抑制CRC细胞系中TGF-β1诱导的EMT。

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