Harada Oi, Suga Tomoaki, Suzuki Takefumi, Nakamoto Katsuaki, Kobayashi Motohiro, Nomiyama Tetsuo, Nadano Daita, Ohyama Chikara, Fukuda Michiko N, Nakayama Jun
Department of Pathology, Shinshu University School of Medicine, Matsumoto, Japan.
Int J Cancer. 2007 Sep 1;121(5):1072-8. doi: 10.1002/ijc.22821.
Trophinin is a unique adhesion molecule expressed by human trophoblastic cells. Its activity and in vivo expression pattern implicate trophinin in the initial attachment of trophectoderm cells to maternal epithelia. Subsequent to apical adhesion, trophoblasts aggressively invade maternal tissue to form the placenta, a process resembling tumor invasion. Here, we report that trophinin is expressed in tumors from 64% of colon cancer patients (n = 50) and high trophinin expression is closely associated with poor prognosis. To determine the link between trophinin expression and malignancy, colon adenocarcinoma SW480 cells were stably transfected with trophinin. An invasion assay showed that trophinin-expressing SW480 cells were more invasive than mock-transfected cells. Microarray analysis comparing SW480 cells transfected with trophinin with mock-transfected cells identified high-mobility group box 1 (HMGB1) as the most significantly elevated transcript. Immunohistochemical analysis of tumors from the colorectal cancer patients confirmed positive correlation of HMGB1 protein expression in the nucleus to trophinin expression in tumor. HMGB1 and its ligand RAGE (the receptor for advanced glycation end product) proteins were coexpressed in 65.6% of trophinin-positive patients (n = 32). These results suggest that trophinin promotes invasion through a mechanism involving HMGB1/RAGE.
滋养蛋白是一种由人滋养层细胞表达的独特黏附分子。其活性和体内表达模式表明滋养蛋白参与了滋养外胚层细胞与母体上皮细胞的初始附着。在顶端黏附之后,滋养层细胞积极侵入母体组织以形成胎盘,这一过程类似于肿瘤侵袭。在此,我们报告滋养蛋白在64%的结肠癌患者(n = 50)的肿瘤中表达,并且高滋养蛋白表达与不良预后密切相关。为了确定滋养蛋白表达与恶性肿瘤之间的联系,用滋养蛋白稳定转染结肠腺癌SW480细胞。侵袭试验表明,表达滋养蛋白的SW480细胞比 mock 转染细胞更具侵袭性。对用滋养蛋白转染的SW480细胞与mock转染细胞进行微阵列分析,确定高迁移率族蛋白B1(HMGB1)是转录水平升高最显著的基因。对结直肠癌患者肿瘤的免疫组织化学分析证实,细胞核中HMGB1蛋白表达与肿瘤中滋养蛋白表达呈正相关。HMGB1及其配体RAGE(晚期糖基化终产物受体)蛋白在65.6%的滋养蛋白阳性患者(n = 32)中共表达。这些结果表明,滋养蛋白通过涉及HMGB1/RAGE的机制促进侵袭。