Fujiwara-Tani Rina, Sasaki Takamitsu, Luo Yi, Goto Kei, Kawahara Isao, Nishiguchi Yukiko, Kishi Shingo, Mori Shiori, Ohmori Hitoshi, Kondoh Masuo, Kuniyasu Hiroki
Department of Molecular Pathology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Jiangsu Province Key Laboratory of Neuroregeneration, Nantong University, Nantong, Jiangsu 226001, China.
Oncotarget. 2018 Dec 21;9(100):37367-37378. doi: 10.18632/oncotarget.26427.
Claudin-4 (CLDN4) is a major epithelial tight junction protein overexpressed in many cancers to maintain the tumor environment. In this report, we aimed to determine the efficacy of targeting CLDN4 in colorectal cancer (CRC) using an anti-CLDN4 extracellular domain antibody, 4D3. CLDN4 was upregulated in CRC metastatic foci. CLDN4 expression in CRC cells was reduced by upregulation of TNFα, which was induced by enterotoxin produced by gut flora. In a nude mouse liver metastasis model, inhibition of metastasis was increased by combination treatment with 5-fluorouracil (FU) and 4D3 compared to that with 5-FU alone. Moreover, combination treatment with 4D3 and anti-epithelial growth factor receptor (EGFR) antibody C225 resulted in more pronounced inhibition of sphere formation and tumor growth in nude mice compared to that observed with C225 alone. Moreover, the time interval between the administration of 4D3 and that of C225 was important for maximizing the C225-induced inhibition of EGFR phosphorylation. In a nude mouse model, sequential treatment with 4D3 and C225 with a 6-h time interval resulted in more pronounced inhibition of tumor growth than concurrent treatment. These findings suggest that the targeting of CLDN4 enhances the antitumoral effects of chemotherapeutic agents and molecular targeting antibodies when used in combination.
紧密连接蛋白4(CLDN4)是一种主要的上皮紧密连接蛋白,在许多癌症中过度表达以维持肿瘤环境。在本报告中,我们旨在确定使用抗CLDN4细胞外结构域抗体4D3靶向CLDN4在结直肠癌(CRC)中的疗效。CLDN4在CRC转移灶中上调。肠道菌群产生的肠毒素诱导TNFα上调,从而降低了CRC细胞中CLDN4的表达。在裸鼠肝转移模型中,与单独使用5-氟尿嘧啶(FU)相比,5-氟尿嘧啶(FU)与4D3联合治疗可增强对转移的抑制作用。此外,与单独使用C225相比,4D3与抗上皮生长因子受体(EGFR)抗体C225联合治疗在裸鼠中对球体形成和肿瘤生长的抑制作用更明显。此外,4D3与C225给药的时间间隔对于最大化C225诱导的EGFR磷酸化抑制作用很重要。在裸鼠模型中,4D3与C225以6小时的时间间隔序贯治疗比同时治疗对肿瘤生长的抑制作用更明显。这些发现表明,靶向CLDN4在联合使用时可增强化疗药物和分子靶向抗体的抗肿瘤作用。