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Influence of SHH/GLI1 axis on EMT mediated migration and invasion of breast cancer cells

机译:SHH / GLI1轴对EMT介导的乳腺癌细胞迁移和侵袭的影响

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摘要

Sonic Hedgehog signaling is critical for breast morphogenesis and cancer. The present study was conducted to explore the influence of SHH/GLI1 axis on epithelial mesenchymal transition and invasion in breast cancer cells. SHH/GLI1 positive samples demonstrated high expression of Snail and Vimentin with relatively low expression of E-cadherin. Overexpression of Vimentin and Snail in SHH/GLI1 positive patients was also associated with poor overall survival. Interestingly, GANT61 (GLI1 inhibitor) exposure significantly reduced cell viability and induced apoptosis at 10 µM. Suppression of Hedgehog pathway either by CRISPR mediated SHH knock out or GANT61 altered regulation of EMT markers in breast cancer cells. Moreover, in-activation of SHH/GLI1 axis also significantly restricted cell migration and invasiveness. These findings suggest that targeting SHH/GLI1 axis alters expression of EMT markers and abrogates neoplastic invasion in breast cancer cells.
机译:声波刺猬信号对于乳腺形态发生和癌症至关重要。本研究旨在探讨SHH / GLI1轴对乳腺癌细胞上皮间质转化和侵袭的影响。 SHH / GLI1阳性样品显示Snail和波形蛋白高表达,而E-钙粘蛋白表达相对低。 SHH / GLI1阳性患者中波形蛋白和蜗牛蛋白的过表达也与总体生存期差有关。有趣的是,GANT61(GLI1抑制剂)的暴露显着降低了细胞活力,并在10μm的诱导细胞凋亡。通过CRISPR介导的SHH敲除或GANT61抑制刺猬通路改变了乳腺癌细胞中EMT标记的调控。此外,SHH / GLI1轴的失活也大大限制了细胞迁移和侵袭性。这些发现表明,靶向SHH / GLI1轴可改变EMT标记的表达并消除乳腺癌细胞中的肿瘤侵袭。

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