Ochoa-Alvarez Jhon A, Krishnan Harini, Pastorino John G, Nevel Evan, Kephart David, Lee Joseph J, Retzbach Edward P, Shen Yongquan, Fatahzadeh Mahnaz, Baredes Soly, Kalyoussef Evelyne, Honma Masaru, Adelson Martin E, Kaneko Mika K, Kato Yukinari, Young Mary Ann, Deluca-Rapone Lisa, Shienbaum Alan J, Yin Kingsley, Jensen Lasse D, Goldberg Gary S
Departments of Molecular Biology, Cell Biology, and Pathology, School of Osteopathic Medicine, Rowan University, Stratford, NJ, USA.
Department of Diagnostic Sciences, Rutgers School of Dental Medicine, Newark, NJ, USA.
Oncotarget. 2015 Apr 20;6(11):9045-60. doi: 10.18632/oncotarget.3515.
Podoplanin (PDPN) is a unique transmembrane receptor that promotes tumor cell motility. Indeed, PDPN may serve as a chemotherapeutic target for primary and metastatic cancer cells, particularly oral squamous cell carcinoma (OSCC) cells that cause most oral cancers. Here, we studied how a monoclonal antibody (NZ-1) and lectin (MASL) that target PDPN affect human OSCC cell motility and viability. Both reagents inhibited the migration of PDPN expressing OSCC cells at nanomolar concentrations before inhibiting cell viability at micromolar concentrations. In addition, both reagents induced mitochondrial membrane permeability transition to kill OSCC cells that express PDPN by caspase independent nonapoptotic necrosis. Furthermore, MASL displayed a surprisingly robust ability to target PDPN on OSCC cells within minutes of exposure, and significantly inhibited human OSCC dissemination in zebrafish embryos. Moreover, we report that human OSCC cells formed tumors that expressed PDPN in mice, and induced PDPN expression in infiltrating host murine cancer associated fibroblasts. Taken together, these data suggest that antibodies and lectins may be utilized to combat OSCC and other cancers that express PDPN.
血小板反应蛋白-1结合蛋白(PDPN)是一种独特的跨膜受体,可促进肿瘤细胞的运动。实际上,PDPN可能作为原发性和转移性癌细胞的化疗靶点,尤其是导致大多数口腔癌的口腔鳞状细胞癌(OSCC)细胞。在此,我们研究了靶向PDPN的单克隆抗体(NZ-1)和凝集素(MASL)如何影响人OSCC细胞的运动和活力。在微摩尔浓度抑制细胞活力之前,两种试剂均在纳摩尔浓度下抑制表达PDPN的OSCC细胞的迁移。此外,两种试剂均诱导线粒体膜通透性转变,通过不依赖半胱天冬酶的非凋亡性坏死杀死表达PDPN的OSCC细胞。此外,MASL在暴露数分钟内就显示出惊人的强大能力来靶向OSCC细胞上的PDPN,并显著抑制人OSCC在斑马鱼胚胎中的扩散。此外,我们报告人OSCC细胞在小鼠体内形成表达PDPN的肿瘤,并在浸润的宿主鼠癌相关成纤维细胞中诱导PDPN表达。综上所述,这些数据表明抗体和凝集素可用于对抗OSCC和其他表达PDPN的癌症。