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Molecular Bases for the Regulation of NKG2D Ligands in Cancer

机译:调节NKG2D配体在癌症中的分子基础。

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摘要

NKG2D is an activating receptor expressed by NK and T cells primarily involved in the elimination of transformed and infected cells. NKG2D ligands are self-proteins restrictedly expressed in healthy tissues, but induced in response to signaling pathways commonly associated with transformation. Proliferative, tumor suppressor, and stress signaling pathways linked to the tumorigenic process induce the expression of NKG2D ligands, initiating an immune response against the incipient tumor. Nevertheless, the activity of NKG2D ligands is counter-regulated in vivo by the immunoediting of cancer cells, resulting in the expression of multiple mechanisms of immune evasion in advanced tumors. The redundancy of NKG2D ligands, besides increasing the complexity of their regulation, may impair the generation of these immune evasion mechanisms. In this review, we attempt to integrate the mechanisms and pathways involved in the regulation of NKG2D ligand expression in cancer.
机译:NKG2D是由NK和T细胞表达的激活受体,主要参与消除转化和感染的细胞。 NKG2D配体是在健康组织中受限制表达的自身蛋白,但在响应通常与转化相关的信号传导途径时被诱导。与致瘤过程相关的增殖,肿瘤抑制和应激信号通路诱导NKG2D配体的表达,从而引发针对初期肿瘤的免疫反应。尽管如此,NKG2D配体的活性在体内通过癌细胞的免疫编辑被反调节,导致晚期肿瘤中多种逃避免疫的机制表达。 NKG2D配体的冗余性,除了增加其调控的复杂性外,还可能会损害这些免疫逃逸机制的产生。在这篇综述中,我们试图整合参与调节NKG2D配体在癌症中的表达的机制和途径。

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