Department of Oral Science, Graduate School of Medicine, Chiba University, Chiba, Japan.
Department of Dentistry and Oral-Maxillofacial Surgery, Chiba University Hospital, Chiba, Japan.
Exp Cell Res. 2018 Jul 1;368(1):119-125. doi: 10.1016/j.yexcr.2018.04.021. Epub 2018 Apr 19.
Multiple coagulation factor deficiency protein 2 (MCFD2), a binding partner of lectin mannose binding 1 (LMAN1), causes combined deficiencies of coagulation factors V and VIII. MCFD2 function in inherited hematologic disorders is well elucidated; however, little is known about its role in human tumorigenesis. The aim of the current study was to investigate the states of MCFD2 in oral squamous cell carcinoma (OSCC). The expression of MCFD2 was up-regulated significantly in all cell lines examined. Evaluation of the cellular functions associated with tumoral metastasis showed that MCFD2 knockdown (shMCFD2) cells exhibited significantly lower cellular invasiveness and migration and higher cellular adhesion compared with shControl cells. Of note, shMCFD2 cells also showed weak immunoreactivity of LMAN1 and a lower secretion level of galactoside-binding soluble 3 binding protein (LGALS3BP). In addition to in vitro validation, clinical data on 70 patients with OSCC indicated that state of MCFD2 expression level is associated with regional lymph node metastasis. Altogether, we have demonstrated that MCFD2 promotes cancer metastasis by regulating LMAN1 and LGALS3BP expression levels. Hence, MCFD2 may represent a promising candidate for a novel therapeutic target for patients with metastatic OSCCs.
多种凝血因子缺乏蛋白 2(MCFD2)是凝集素甘露糖结合蛋白 1(LMAN1)的结合伴侣,可导致凝血因子 V 和 VIII 联合缺乏。MCFD2 在遗传性血液疾病中的功能已得到充分阐明;然而,其在人类肿瘤发生中的作用知之甚少。本研究旨在探讨 MCFD2 在口腔鳞状细胞癌(OSCC)中的状态。在所有检测的细胞系中,MCFD2 的表达均显著上调。评估与肿瘤转移相关的细胞功能表明,与 shControl 细胞相比,MCFD2 敲低(shMCFD2)细胞的细胞侵袭和迁移能力显著降低,而细胞黏附能力显著升高。值得注意的是,shMCFD2 细胞还表现出 LMAN1 的弱免疫反应性和半乳糖结合可溶性 3 结合蛋白(LGALS3BP)的低分泌水平。除了体外验证外,对 70 例 OSCC 患者的临床数据表明,MCFD2 表达水平与区域淋巴结转移有关。综上所述,我们已经证明 MCFD2 通过调节 LMAN1 和 LGALS3BP 的表达水平促进癌症转移。因此,MCFD2 可能成为转移性 OSCC 患者新的治疗靶点。