Koga Kaori, Nabeshima Kazuki, Aoki Mikiko, Kawakami Takehito, Hamasaki Makoto, Toole Bryan P, Nakayama Juichiro, Iwasaki Hiroshi
Department of Pathology, Fukuoka University School of medicine, Fukuoka, Japan.
Int J Cancer. 2007 Feb 15;120(4):761-8. doi: 10.1002/ijc.22412.
Emmprin is a transmembrane glycoprotein on tumor cells that stimulates peritumoral fibroblasts to produce matrix metalloproteinases (MMPs). Emmprin and the induced MMPs play a crucial role in tumor progression, invasion and metastasis of human carcinomas (epithelial malignancies). However, only a few reports have addressed its role in soft tissue sarcomas. This study investigated the expression and role of emmprin in epithelioid sarcoma (ES). Immunoblot studies of 2 ES cell lines showed that they express emmprin, and co-culture of these ES cells with dermal fibroblasts resulted in upregulation of gelatinase A (MMP-2) in fibroblasts, as shown by zymography, immunoblotting and enzyme immunoassay. This stimulation was inhibited by an activity-blocking peptide against emmprin and by antiemmprin antibody. In addition, in vivo, immunohistochemical analysis of 5 ES patient cases demonstrated diffuse emmprin expression in ES cells and MMP-2 expression in both ES cells and peritumoral fibroblasts. The histopathological findings that peritumoral fibroblasts that were not in direct contact with emmprin-expressing ES cells exhibit upregulated MMP-2 prompted us to look for a soluble form of emmprin. Soluble full-length emmprin released from ES cells was detected in conditioned medium and shown to stimulate MMP-2 production by fibroblasts. In conclusion, emmprin is expressed in ES in both membrane and soluble forms and stimulates MMP-2 production via interactions with fibroblasts, which could play a role in ES cell stromal invasion and vascular involvement.
埃姆普林是肿瘤细胞上的一种跨膜糖蛋白,可刺激肿瘤周围的成纤维细胞产生基质金属蛋白酶(MMPs)。埃姆普林和诱导产生的MMPs在人类癌症(上皮性恶性肿瘤)的肿瘤进展、侵袭和转移中起关键作用。然而,只有少数报告涉及它在软组织肉瘤中的作用。本研究调查了埃姆普林在上皮样肉瘤(ES)中的表达及作用。对2种ES细胞系的免疫印迹研究表明它们表达埃姆普林,这些ES细胞与真皮成纤维细胞共培养导致成纤维细胞中明胶酶A(MMP-2)上调,这通过酶谱分析、免疫印迹和酶免疫测定得以证实。这种刺激被一种针对埃姆普林的活性阻断肽和抗埃姆普林抗体所抑制。此外,在体内,对5例ES患者病例的免疫组织化学分析显示ES细胞中埃姆普林弥漫性表达,ES细胞和肿瘤周围成纤维细胞中均有MMP-2表达。肿瘤周围未与表达埃姆普林的ES细胞直接接触的成纤维细胞MMP-2上调这一组织病理学发现促使我们寻找埃姆普林可溶形式。在条件培养基中检测到ES细胞释放的可溶性全长埃姆普林,其可刺激成纤维细胞产生MMP-2。总之,埃姆普林在ES中以膜结合和可溶两种形式表达,并通过与成纤维细胞相互作用刺激MMP-2产生,这可能在ES细胞的基质侵袭和血管侵犯中发挥作用。