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RGD 钙黏蛋白和α2β1 整合素在癌症转移中的作用:危险的联姻。

RGD cadherins and α2β1 integrin in cancer metastasis: A dangerous liaison.

机构信息

Department of Molecular Biomedicine, Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu 9, 28039 Madrid, Spain.

Department of Molecular Biomedicine, Centro de Investigaciones Biológicas, CSIC, Ramiro de Maeztu 9, 28039 Madrid, Spain.

出版信息

Biochim Biophys Acta Rev Cancer. 2018 Apr;1869(2):321-332. doi: 10.1016/j.bbcan.2018.04.005. Epub 2018 Apr 17.

DOI:10.1016/j.bbcan.2018.04.005
PMID:29673969
Abstract

We propose a new cadherin family classification comprising epithelial cadherins (cadherin 17 [CDH17], cadherin 16, VE-cadherin, cadherin 6 and cadherin 20) containing RGD motifs within their sequences. Expression of some RGD cadherins is associated with aggressive forms of cancer during the late stages of metastasis, and CDH17 and VE-cadherin have emerged as critical actors in cancer metastasis. After binding to α2β1 integrin, these cadherins promote integrin β1 activation, and thereby cell adhesion, invasion and proliferation, in liver and lung metastasis. Activation of α2β1 integrin provokes an affinity increase for type IV collagen, a major component of the basement membrane and a critical partner for cell anchoring in liver and other metastatic organs. Activation of α2β1 integrin by RGD motifs breaks an old paradigm of integrin classification and supports an important role of this integrin in cancer metastasis. Recently, synthetic peptides containing the RGD motif of CDH17 elicited highly specific and selective antibodies that block the ability of CDH17 RGD to activate α2β1 integrin. These monoclonal antibodies inhibit metastatic colonization in orthotopic mouse models of liver and lung metastasis for colorectal cancer and melanoma, respectively. Hopefully, blocking the cadherin RGD ligand capacity will give us control over the integrin activity in solid tumors metastasis, paving the way for development of new agents of cancer treatment.

摘要

我们提出了一种新的钙黏蛋白家族分类法,包括含有 RGD 基序的上皮钙黏蛋白(钙黏蛋白 17 [CDH17]、钙黏蛋白 16、VE-钙黏蛋白、钙黏蛋白 6 和钙黏蛋白 20)。这些 RGD 钙黏蛋白的一些表达与转移后期侵袭性癌症有关,CDH17 和 VE-钙黏蛋白已成为癌症转移的关键因素。与α2β1 整合素结合后,这些钙黏蛋白促进整合素β1 的激活,从而促进肝和肺转移中的细胞黏附、侵袭和增殖。α2β1 整合素的激活引发对 IV 型胶原的亲和力增加,IV 型胶原是基底膜的主要成分,也是肝和其他转移器官中细胞锚定的关键伴侣。RGD 基序激活 α2β1 整合素打破了整合素分类的旧范式,并支持该整合素在癌症转移中的重要作用。最近,含有 CDH17 的 RGD 基序的合成肽引发了高度特异性和选择性的抗体,阻断了 CDH17 RGD 激活 α2β1 整合素的能力。这些单克隆抗体抑制了结直肠癌和黑色素瘤的肝和肺转移的原位小鼠模型中的转移性定植。希望阻断钙黏蛋白 RGD 配体能力将使我们能够控制实体瘤转移中整合素的活性,为开发新的癌症治疗药物铺平道路。

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