The Breast Cancer Now Toby Robins Research Centre, The Institute of Cancer Research, London, United Kingdom.
Division of Vascular Oncology and Metastasis (DKFZ-ZMBH Alliance), German Cancer Research Center, Heidelberg, Germany. Department of Vascular Biology and Tumor Angiogenesis (CBTM), Medical Faculty Mannheim, Heidelberg University, Heidelberg, Germany.
Cancer Res. 2016 Sep 15;76(18):5313-25. doi: 10.1158/0008-5472.CAN-16-0932.
Metastasis is a multistep process that is critically dependent on the interaction of metastasizing tumor cells with cells in the local microenvironment. Within this tumor stroma, vessel-associated pericytes and myofibroblasts share a number of traits, including the upregulated expression of the transmembrane receptor endosialin (CD248). Comparative experiments in wild-type and endosialin-deficient mice revealed that stromal endosialin does not affect primary tumor growth but strongly promotes spontaneous metastasis. Mechanistically, endosialin-expressing pericytes in the primary tumor facilitate distant site metastasis by promoting tumor cell intravasation in a cell contact-dependent manner, resulting in elevated numbers of circulating tumor cells. Corresponding to these preclinical experiments, in independent cohorts of primary human breast cancers, upregulated endosialin expression significantly correlates with increased metastasis and poorer patient survival. Together, the data demonstrate a critical role for endosialin-expressing primary tumor pericytes in mediating metastatic dissemination and identify endosialin as a promising therapeutic target in breast cancer. Cancer Res; 76(18); 5313-25. ©2016 AACR.
转移是一个多步骤的过程,严重依赖于转移肿瘤细胞与局部微环境中细胞的相互作用。在这个肿瘤基质中,血管相关的周细胞和成肌纤维细胞具有许多共同特征,包括跨膜受体内皮细胞唾液酸糖蛋白(endosialin,CD248)的上调表达。在野生型和内皮细胞缺陷型小鼠的比较实验中发现,基质内皮细胞不会影响原发肿瘤的生长,但强烈促进自发性转移。从机制上讲,原发肿瘤中表达内皮细胞的周细胞通过以细胞接触依赖性的方式促进肿瘤细胞的浸润,从而促进远处部位转移,导致循环肿瘤细胞数量增加。与这些临床前实验相对应的是,在独立的原发性人乳腺癌队列中,上调的内皮细胞表达与转移增加和患者生存不良显著相关。总之,这些数据表明,表达内皮细胞的原发性肿瘤周细胞在介导转移扩散中起着关键作用,并将内皮细胞鉴定为乳腺癌有前途的治疗靶点。Cancer Res; 76(18); 5313-25. ©2016 AACR.