首页> 美国卫生研究院文献>BMC Cancer >Protein kinase C inhibitor Gö6976 but not Gö6983 induces the reversion of E- to N-cadherin switch and metastatic phenotype in melanoma: identification of the role of protein kinase D1
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Protein kinase C inhibitor Gö6976 but not Gö6983 induces the reversion of E- to N-cadherin switch and metastatic phenotype in melanoma: identification of the role of protein kinase D1

机译:蛋白激酶C抑制剂Gö6976而非Gö6983诱导黑素瘤中E-向N-钙黏着蛋白转换和转移表型的逆转:确定蛋白激酶D1的作用

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摘要

BackgroundMelanoma is a highly metastatic type of cancer that is resistant to all standard anticancer therapies and thus has a poor prognosis. Therefore, metastatic melanoma represents a significant clinical problem and requires novel and effective targeted therapies. The protein kinase C (PKC) family comprises multiple isoforms of serine/threonine kinases that possess distinct roles in cancer development and progression. In this study, we determined whether inhibition of PKC could revert a major process required for melanoma progression and metastasis; i.e. the E- to N-cadherin switch.
机译:背景黑色素瘤是一种高度转移性癌症,对所有标准抗癌疗法均具有抵抗力,因此预后较差。因此,转移性黑素瘤代表了重要的临床问题,需要新颖有效的靶向治疗。蛋白激酶C(PKC)家族包含丝氨酸/苏氨酸激酶的多种同工型,它们在癌症的发生和发展中具有独特的作用。在这项研究中,我们确定了抑制PKC是否可以逆转黑色素瘤进展和转移所需的主要过程。即E-到N-钙粘着蛋白开关。

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