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CLEC-2与血小板反应蛋白-1相互作用在肿瘤进展中的作用。

Roles of the CLEC-2-podoplanin interaction in tumor progression.

作者信息

Suzuki-Inoue Katsue

机构信息

a Department of Clinical and Laboratory Medicine, Faculty of Medicine , University of Yamanashi , Yamanashi , Japan.

出版信息

Platelets. 2018 Jun 4:1-7. doi: 10.1080/09537104.2018.1478401.

Abstract

Podoplanin is a type-I transmembrane sialomucin-like glycoprotein expressed on the surface of several kinds of tumor cells. The podoplanin receptor is a platelet activation receptor known as C-type lectin-like receptor 2 (CLEC-2), which has been identified as a receptor for the platelet-activating snake venom protein rhodocytin. CLEC-2 is highly expressed in platelets and megakaryocytes and expressed at lower levels in liver Kupffer cells. Podoplanin is expressed in certain types of tumor cells, including squamous cell carcinomas, seminomas, and brain tumors. Podoplanin is also expressed in a wide range of normal cells, including fibroblastic reticular cells in lymph nodes, kidney podocytes, and lymphatic endothelial cells, but not vascular endothelial cells. Metastasis of podoplanin-positive lung tumors injected from the tail vein is greatly inhibited in CLEC-2-depleted mice or in anti-podoplanin antibody-treated mice. These findings suggest that the CLEC-2-podoplanin interaction facilitates hematogenous tumor metastasis. Platelets may increase the survival of tumor cells by covering tumor cells and physically protecting them from shear stress or immune cells in the bloodstream. Alternatively, platelets may stimulate the epithelial-mesenchymal transition of tumor cells to facilitate their extravasation from blood vessels. Cell proliferation is stimulated in podoplanin-expressing tumor cells by the coculture with platelets, but the effects of the CLEC-2-podoplanin interaction on tumor growth in vivo are not yet resolved. It is possible that the CLEC-2-podoplanin interaction facilitates tumor-related thrombosis, subsequent inflammation, inflammation-induced cachexia, and reduced survival. Considering these findings, anti-podoplanin and anti-CLEC-2 drugs are promising therapies for the prevention of tumor metastasis, progression, and tumor-related symptoms, which may result in longer survival in cancer patients. There are advantages and disadvantages of anti-podoplanin vs. anti-CLEC-2 therapy. Side effects in podoplanin-expressing normal tissues due to treatment with anti-podoplanin and temporal thrombocytopenia due to treatment with anti-CLEC2 are potential problems, although solutions to these problems have been reported.

摘要

血小板内皮细胞黏附分子是一种I型跨膜唾液酸黏蛋白样糖蛋白,表达于多种肿瘤细胞表面。血小板内皮细胞黏附分子受体是一种血小板活化受体,称为C型凝集素样受体2(CLEC-2),它已被确定为血小板活化蛇毒蛋白红藻凝集素的受体。CLEC-2在血小板和巨核细胞中高表达,在肝库普弗细胞中表达水平较低。血小板内皮细胞黏附分子在某些类型的肿瘤细胞中表达,包括鳞状细胞癌、精原细胞瘤和脑肿瘤。血小板内皮细胞黏附分子也在多种正常细胞中表达,包括淋巴结中的成纤维网状细胞、肾足细胞和淋巴管内皮细胞,但不在血管内皮细胞中表达。从尾静脉注射的血小板内皮细胞黏附分子阳性肺肿瘤在CLEC-2缺陷小鼠或抗血小板内皮细胞黏附分子抗体处理的小鼠中转移受到极大抑制。这些发现表明CLEC-2-血小板内皮细胞黏附分子相互作用促进血行性肿瘤转移。血小板可能通过覆盖肿瘤细胞并在物理上保护它们免受血流中的剪切应力或免疫细胞的影响来增加肿瘤细胞的存活。或者,血小板可能刺激肿瘤细胞的上皮-间质转化,以促进它们从血管外渗。与血小板共培养可刺激表达血小板内皮细胞黏附分子的肿瘤细胞的增殖,但CLEC-2-血小板内皮细胞黏附分子相互作用对体内肿瘤生长的影响尚未明确。CLEC-2-血小板内皮细胞黏附分子相互作用可能促进肿瘤相关血栓形成、随后的炎症、炎症诱导的恶病质和生存率降低。考虑到这些发现,抗血小板内皮细胞黏附分子和抗CLEC-2药物有望用于预防肿瘤转移、进展和肿瘤相关症状,这可能会延长癌症患者的生存期。抗血小板内皮细胞黏附分子治疗与抗CLEC-2治疗各有优缺点。抗血小板内皮细胞黏附分子治疗导致表达血小板内皮细胞黏附分子的正常组织出现副作用,以及抗CLEC2治疗导致暂时血小板减少是潜在问题,尽管已经报道了这些问题的解决方案。

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