首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Grape Seed Proanthocyanidins Inhibit Migration and Invasion of Bladder Cancer Cells by Reversing EMT through Suppression of TGF- β Signaling Pathway
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Grape Seed Proanthocyanidins Inhibit Migration and Invasion of Bladder Cancer Cells by Reversing EMT through Suppression of TGF- β Signaling Pathway

机译:通过抑制TGF-β信号通路,通过抑制EMT来抑制膀胱癌细胞的迁移和侵袭膀胱癌细胞的迁移和侵袭

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Bladder cancer (BC) is the most common cancer of the urinary system. Despite advances in diagnosis and therapy, the prognosis is still poor because of recurrence and metastasis. Epithelial-mesenchymal transition (EMT) is considered to play an important role in the invasion and metastasis of BC. Grape seed proanthocyanidins (GSPs) exhibit chemopreventive and chemotherapeutic activities against several types of cancer. However, their effects and underlying mechanisms on the invasive potential of BC remain unclear. In this study, we found that GSPs inhibited migration, invasion, and MMP-2/-9 secretion of both T24 and 5637 bladder cancer cells at noncytotoxic concentrations. We also discovered that 5637 cells were more suitable than T24 cells for the EMT study. Further study showed that GSPs inhibited EMT by reversing the TGF- β -induced morphological change and upregulation of mesenchymal markers N-cadherin, vimentin, and Slug as well as downregulation of epithelial markers E-cadherin and ZO-1 in 5637 cells. GSPs also inhibited TGF- β -induced phosphorylation of Smad2/3, Akt, Erk, and p38 in 5637 cells without affecting the expression of total Smad2/3, Akt, Erk, and p38. Taken together, the results of the present study demonstrate that GSPs effectively inhibit the migration and invasion of BC cells by reversing EMT through suppression of the TGF- β signaling pathway, which indicates that GSPs could be developed as a potential chemopreventive and therapeutic agent against bladder cancer.
机译:膀胱癌(BC)是泌尿系统中最常见的癌症。尽管诊断和治疗进展,但由于复发和转移,预后仍然贫困。上皮 - 间充质转换(EMT)被认为在BC的侵袭和转移中发挥着重要作用。葡萄籽花香素蛋白(GSP)表现出用于若干类型的癌症的化学预防和化学治疗活动。然而,他们的效果和潜在的机制对BC的侵入性潜力仍不清楚。在这项研究中,我们发现GSP在非毒性浓度下抑制T24和5637膀胱癌细胞的迁移,侵袭和MMP-2 / -9分泌。我们还发现5637个细胞比EMT研究更适合于T24细胞。进一步的研究表明,通过逆转TGF-β-屈服的形态变化和间充质标记物的形态变化和上调,抑制蛋白,拉丝蛋白和5637细胞中的上皮标记物和ZO-1的下调,GSP通过抑制EMT。 GSPS还抑制了TGF-β-诱导的Smad2 / 3,AKT,ERK和P38在5637个细胞中的磷酸化而不影响总Smad2 / 3,Akt,Erk和P38的表达。在一起,本研究结果表明,GSP通过抑制TGF-β信号通路通过逆转EMT有效抑制BC细胞的迁移和侵袭,这表明GSP可以作为潜在的化学预防和治疗剂对抗膀胱开发癌症。

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