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首页> 外文期刊>Biochemical and Biophysical Research Communications >Knockdown of aristaless-like homeobox1 inhibits epithelial-mesenchymal transition through Wnt/beta-catenin signaling pathway in melanoma cells
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Knockdown of aristaless-like homeobox1 inhibits epithelial-mesenchymal transition through Wnt/beta-catenin signaling pathway in melanoma cells

机译:劣质的Homeobox1敲低通过黑素瘤细胞中的Wnt /β-catenin信号传导途径抑制上皮 - 间充质转换

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Aristaless-like homeobox1 (ALX1), a member of the ALX family, is capable of mediating survival and development of mesenchyme-derived elements in vertebrates and its mutation will prevent the fusion of frontonasal and maxillary elements. Recently, ALX1 has been reported to be associated with cancer progression. However, the specific roles of ALX1 in melanoma remain unclear. In this study, we investigated the expression pattern and biological functions of ALX1 in melanoma. We found that ALX1 was highly expressed in melanoma tissues and cell lines. Knockdown of ALX1 suppressed the proliferation and invasion of melanoma cells. Furthermore, we showed that ALX1 knockdown reversed the epithelial-mesenchymal transition (EMT) process in melanoma cells, which might be attributed to inactivation of the Wnt/beta-catenin pathway. Taken together, this study provided a new insight into the role of ALX1 as a therapeutic target for melanoma treatment. (C) 2019 Elsevier Inc. All rights reserved.
机译:aristaless样的Homeobox1(Alx1)是Alx系列的成员,能够介导脊椎动物中间充质衍生元素的存活率和发育,其突变将防止前进和上颌元素的融合。 最近,据报道,ALX1与癌症进展有关。 然而,ALX1在黑素瘤中的特异性作用仍然不清楚。 在这项研究中,我们研究了黑色素瘤中ALX1的表达模式和生物学功能。 我们发现ALX1在黑色素瘤组织和细胞系中高度表达。 ALX1的敲低抑制了黑色素瘤细胞的增殖和侵袭。 此外,我们表明Alx1敲低逆转了黑色素瘤细胞中的上皮 - 间充质转换(EMT)过程,这可能归因于WNT /β-连环蛋白途径的灭活。 这项研究共同参与了新的洞察Alx1作为黑素瘤治疗治疗靶标的作用。 (c)2019 Elsevier Inc.保留所有权利。

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