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利用 O-聚糖的肿瘤防御系统。

Tumor defense systems using O-glycans.

机构信息

Department of Biochemistry, Oyokyo Kidney Research Institute, 90 Kozawa, Yamazaki, Hirosaki, Aomori 036–8243, Japan.

出版信息

Biol Pharm Bull. 2012;35(10):1633-6. doi: 10.1248/bpb.b12-00367.

Abstract

During the process of hematogenous tumor metastasis, tumor cells that dissociated from the primary site enter the blood vessels and are exposed to innate immune systems in host blood circulation. In the innate immune systems, natural killer (NK) cells play a major role in rejecting tumors and suppressing metastasis. To establish metastasis, tumor cells therefore need to defend themselves against tumor rejection by NK cells. It has been recently discovered that some tumor cells develop defense systems against NK cell attack using certain types of cell-surface carbohydrates. The types of carbohydrates attached to cell-surface glycoproteins through serine or threonine residues contain a branch consisting of β-1,6-linkage of N-acetylglucosamine and N-acetylgalactosamine and are designated as core2 O-glycans. Tumor cells expressing core2 O-glycans evade NK cell-mediated tumor rejection, thereby surviving longer in host circulation and acquiring high-metastatic phenotypes. This review explains two types of tumor defense systems against NK cell immunity using core2 O-glycans.

摘要

在血源肿瘤转移的过程中,从原发性肿瘤脱离的肿瘤细胞进入血管,并暴露于宿主血液循环中的固有免疫系统。在固有免疫系统中,自然杀伤 (NK) 细胞在排斥肿瘤和抑制转移方面发挥着重要作用。为了建立转移,肿瘤细胞因此需要保护自己免受 NK 细胞的排斥。最近发现,一些肿瘤细胞使用某些类型的细胞表面碳水化合物来开发针对 NK 细胞攻击的防御系统。通过丝氨酸或苏氨酸残基附着在细胞表面糖蛋白上的碳水化合物类型包含由 N-乙酰葡萄糖胺和 N-乙酰半乳糖胺组成的 β-1,6 键连接的分支,被指定为核心 2 O-聚糖。表达核心 2 O-聚糖的肿瘤细胞逃避 NK 细胞介导的肿瘤排斥,从而在宿主循环中存活更长时间并获得高转移表型。本综述解释了使用核心 2 O-聚糖的两种肿瘤防御系统来对抗 NK 细胞免疫。

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