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Expression of Dickkopf genes is strongly reduced in malignant melanoma

机译:Dickkopf基因的表达在恶性黑色素瘤中大大降低

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摘要

The Dickkopf (DKK) genes were originally identified as factors inducing head formation in Xenopus. The genes code for inhibitors that are involved in Wnt signaling. We speculate that loss of DKK expression plays a role in development or progression of malignant melanoma. Thus, we evaluated melanoma cell lines and tissue samples of malignant melanoma for loss of DKK, especially DKK-3 transcription. We found that DKK-1, -2 and -3 were downregulated or lost in all cell lines and in most of the tumor samples analysed. Reduced DKK-3 expression occurred as early as in primary tumors detected by both immunohistochemical and reverse transcription–polymerase chain reaction RT–PCR analysis. Functional assays with stable DKK-3 transfected cell lines revealed that DKK-3 expression increased cell-cell adhesion and decreased cell migration. Further, downregulation of fibronectin, snail-1 and re-expression of E-cadherin was found in the DKK-3 expressing cell clones supporting a role of DKK-3 in tumor progression. Our studies thus indicate that loss of DKK-3 expression may contribute to melanoma progression.
机译:Dickkopf(DKK)基因最初被确定为诱导非洲爪蟾头部形成的因素。该基因编码参与Wnt信号转导的抑制剂。我们推测,DKK表达的丧失在恶性黑色素瘤的发生或发展中起一定作用。因此,我们评估了黑色素瘤细胞系和恶性黑色素瘤组织样品中DKK的丢失,尤其是DKK-3转录的丢失。我们发现,在所有细胞系和分析的大多数肿瘤样本中,DKK-1,-2和-3均下调或丢失。通过免疫组化和逆转录-聚合酶链反应RT-PCR分析发现,DKK-3表达降低最早发生在原发肿瘤中。用稳定的DKK-3转染的细胞系进行的功能测定表明,DKK-3的表达增加了细胞间的粘附力并减少了细胞迁移。此外,在表达DKK-3的细胞克隆中发现纤连蛋白,snail-1的下调和E-钙粘着蛋白的重新表达支持DKK-3在肿瘤进展中的作用。因此,我们的研究表明,DKK-3表达的丧失可能有助于黑色素瘤的进展。

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