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活化白细胞细胞黏附分子的基质表达促进肺肿瘤生长和转移。

Stromal Expression of Activated Leukocyte Cell Adhesion Molecule Promotes Lung Tumor Growth and Metastasis.

作者信息

Willrodt Ann-Helen, Beffinger Michal, Vranova Martina, Protsyuk Darya, Schuler Katja, Jadhav Maria, Heikenwalder Mathias, van den Broek Maries, Borsig Lubor, Halin Cornelia

机构信息

Institute of Pharmaceutical Sciences, ETH Zurich (Swiss Federal Institute of Technology), Zurich, Switzerland.

Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland.

出版信息

Am J Pathol. 2017 Nov;187(11):2558-2569. doi: 10.1016/j.ajpath.2017.07.008. Epub 2017 Aug 17.

DOI:10.1016/j.ajpath.2017.07.008
PMID:28822802
Abstract

Activated leukocyte cell adhesion molecule (ALCAM) is expressed on various cell types, including leukocytes, endothelial cells, and certain tumor cells. Although ALCAM expression on tumor cells has been linked to tumor invasion and metastatic spread, the contribution of ALCAM expressed in cells forming the tumor stroma to cancer progression has not been investigated. In this study, ALCAM-deficient (ALCAM) mice were used to evaluate the role of ALCAM in lung tumor growth and metastasis. ALCAM mice displayed an altered blood vascular network in the lung and the diaphragm, indicative of an angiogenetic defect. The absence of ALCAM expression in cells forming the stromal tumor microenvironment profoundly affected lung tumor growth in three different i.v. metastasis models. In the case of Lewis lung carcinoma (LLC), an additional defect in tumor cell homing to the lungs and a resulting reduction in the number of lung tumor nodules were observed. Similarly, when LLC cells were implanted subcutaneously for the study of spontaneous tumor cell metastasis, the rate of LLC metastasis to the lungs was profoundly reduced in ALCAM mice. Taken together, our work demonstrates for the first time the in vivo contribution of ALCAM to angiogenesis and reveals a novel role of stromally expressed ALCAM in supporting tumor growth and metastatic spread.

摘要

活化白细胞细胞黏附分子(ALCAM)在多种细胞类型上表达,包括白细胞、内皮细胞和某些肿瘤细胞。虽然肿瘤细胞上的ALCAM表达与肿瘤侵袭和转移扩散有关,但肿瘤基质中表达的ALCAM对癌症进展的作用尚未得到研究。在本研究中,使用ALCAM缺陷型(ALCAM-/-)小鼠来评估ALCAM在肺肿瘤生长和转移中的作用。ALCAM-/-小鼠的肺和膈肌中的血管网络发生改变,表明存在血管生成缺陷。在三种不同的静脉转移模型中,肿瘤基质微环境中形成细胞缺乏ALCAM表达对肺肿瘤生长产生了深远影响。在Lewis肺癌(LLC)模型中,还观察到肿瘤细胞归巢至肺的额外缺陷以及肺肿瘤结节数量的减少。同样,当皮下植入LLC细胞以研究自发肿瘤细胞转移时,ALCAM-/-小鼠中LLC转移至肺的速率显著降低。综上所述,我们的工作首次证明了ALCAM在体内对血管生成的作用,并揭示了基质表达的ALCAM在支持肿瘤生长和转移扩散中的新作用。

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