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血小板,作为固着性和播散性肿瘤细胞的恒定且协同的伙伴,对肿瘤微环境起着至关重要的作用。

Platelets, Constant and Cooperative Companions of Sessile and Disseminating Tumor Cells, Crucially Contribute to the Tumor Microenvironment.

作者信息

Obermann Wolfgang M J, Brockhaus Katrin, Eble Johannes A

机构信息

Institute of Physiological Chemistry and Pathobiochemistry, University of Münster, Münster, Germany.

出版信息

Front Cell Dev Biol. 2021 Apr 16;9:674553. doi: 10.3389/fcell.2021.674553. eCollection 2021.

Abstract

Although platelets and the coagulation factors are components of the blood system, they become part of and contribute to the tumor microenvironment (TME) not only within a solid tumor mass, but also within a hematogenous micrometastasis on its way through the blood stream to the metastatic niche. The latter basically consists of blood-borne cancer cells which are in close association with platelets. At the site of the primary tumor, the blood components reach the TME via leaky blood vessels, whose permeability is increased by tumor-secreted growth factors, by incomplete angiogenic sprouts or by vasculogenic mimicry (VM) vessels. As a consequence, platelets reach the primary tumor via several cell adhesion molecules (CAMs). Moreover, clotting factor VII from the blood associates with tissue factor (TF) that is abundantly expressed on cancer cells. This extrinsic tenase complex turns on the coagulation cascade, which encompasses the activation of thrombin and conversion of soluble fibrinogen into insoluble fibrin. The presence of platelets and their release of growth factors, as well as fibrin deposition changes the TME of a solid tumor mass substantially, thereby promoting tumor progression. Disseminating cancer cells that circulate in the blood stream also recruit platelets, primarily by direct cell-cell interactions via different receptor-counterreceptor pairs and indirectly by fibrin, which bridges the two cell types via different integrin receptors. These tumor cell-platelet aggregates are hematogenous micrometastases, in which platelets and fibrin constitute a particular TME in favor of the cancer cells. Even at the distant site of settlement, the accompanying platelets help the tumor cell to attach and to grow into metastases. Understanding the close liaison of cancer cells with platelets and coagulation factors that change the TME during tumor progression and spreading will help to curb different steps of the metastatic cascade and may help to reduce tumor-induced thrombosis.

摘要

尽管血小板和凝血因子是血液系统的组成部分,但它们不仅成为实体肿瘤块内肿瘤微环境(TME)的一部分并对其产生影响,而且在通过血流到达转移龛的血行微转移灶内也是如此。后者主要由与血小板密切相关的血行癌细胞组成。在原发性肿瘤部位,血液成分通过渗漏的血管进入TME,肿瘤分泌的生长因子、不完全的血管生成芽或血管生成拟态(VM)血管会增加这些血管的通透性。因此,血小板通过几种细胞粘附分子(CAMs)到达原发性肿瘤。此外,血液中的凝血因子VII与癌细胞上大量表达的组织因子(TF)结合。这种外源性凝血酶原酶复合物启动凝血级联反应,该反应包括凝血酶的激活以及可溶性纤维蛋白原转化为不溶性纤维蛋白。血小板的存在及其生长因子的释放,以及纤维蛋白沉积,极大地改变了实体肿瘤块的TME,从而促进肿瘤进展。在血流中循环的播散癌细胞也主要通过不同受体-反受体对的直接细胞间相互作用以及通过纤维蛋白间接招募血小板,纤维蛋白通过不同的整合素受体桥接这两种细胞类型。这些肿瘤细胞-血小板聚集体是血行微转移灶,其中血小板和纤维蛋白构成有利于癌细胞的特定TME。即使在远处的定居部位,伴随的血小板也有助于肿瘤细胞附着并发展为转移灶。了解癌细胞与血小板和凝血因子在肿瘤进展和扩散过程中改变TME的密切联系,将有助于抑制转移级联反应的不同步骤,并可能有助于减少肿瘤诱导的血栓形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9626/8085416/0b9db52bdc7f/fcell-09-674553-g001.jpg

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