Bai Shuang, Sun Shao-Kang, Xu Zhen-Qi, Yan Ying-Bin
Department of Oral and Maxillofacial Surgery, Tianjin Stomatological Hospital, School of Medicine, Nankai University, Tianjin, PR China.
Tianjin Key Laboratory of Oral and Maxillofacial Function Reconstruction, Tianjin, PR China.
Histol Histopathol. 2025 Aug;40(8):1261-1274. doi: 10.14670/HH-18-852. Epub 2024 Nov 25.
Accumulating evidence has implicated matrix metalloproteinases (MMPs) in the progression of human cancers. Matrix metallopeptidase 25 (MMP25) is a membrane-type MMP whose role in tumorigenesis and cancer development is not well understood. Here, we investigated the functions of MMP25 in tongue squamous cell carcinoma (TSCC).
Gene expression was measured using real-time PCR and western blot. CCK-8 and Transwell assays were used to determine the proliferation, migration, and invasion of TSCC cells. An NK cell co-culture experiment was performed to evaluate the killing of TSCC cells by NK cells.
MMP25 had higher expression levels in TSCC tissues than in adjacent non-cancerous tissues. MMP25-overexpressing and MMP25-silenced TSCC cell lines were established by lentiviral transduction. Overexpression of MMP25 promoted proliferation, migration, and invasion of TSCC cells, whereas knockdown of MMP25 had opposite effects. MMP25 modulated the levels of proliferation- and apoptosis-related proteins (PCNA, cyclin D, cyclin B1, p27, and cleaved caspase 3 and 9) and upregulated two invasion-related MMPs (mature MMP2 and MMP9). Additionally, MMP25 promoted tumor growth of TSCC cells in athymic nude mice. Notably, MMP25 upregulated PD-L1 in TSCC cells, attenuated NK cell killing of TSCC cells, and inhibited the secretion of anti-tumor cytokines (TNF-α and IFN-γ). Furthermore, MMP25 promoted the nuclear translocation of NF-κB p65, suggesting that activation of NF-κB signaling may mediate the pro-tumor functions of MMP25 in TSCC.
This study revealed a novel role for MMP25 in TSCC, highlighting the potential of MMP25 as a therapeutic target in TSCC.
越来越多的证据表明基质金属蛋白酶(MMPs)与人类癌症的进展有关。基质金属肽酶25(MMP25)是一种膜型MMP,其在肿瘤发生和癌症发展中的作用尚不清楚。在此,我们研究了MMP25在舌鳞状细胞癌(TSCC)中的功能。
使用实时PCR和蛋白质印迹法测量基因表达。采用CCK-8和Transwell实验来确定TSCC细胞的增殖、迁移和侵袭能力。进行自然杀伤(NK)细胞共培养实验以评估NK细胞对TSCC细胞的杀伤作用。
MMP25在TSCC组织中的表达水平高于相邻的非癌组织。通过慢病毒转导建立了MMP25过表达和MMP25沉默的TSCC细胞系。MMP25的过表达促进了TSCC细胞的增殖、迁移和侵袭,而MMP25的敲低则产生相反的效果。MMP25调节了增殖和凋亡相关蛋白(增殖细胞核抗原、细胞周期蛋白D、细胞周期蛋白B1、p27以及裂解的半胱天冬酶3和9)的水平,并上调了两种侵袭相关的MMPs(成熟的MMP2和MMP9)。此外,MMP25促进了TSCC细胞在无胸腺裸鼠中的肿瘤生长。值得注意的是,MMP25上调了TSCC细胞中的程序性死亡受体配体1(PD-L1),减弱了NK细胞对TSCC细胞的杀伤作用,并抑制了抗肿瘤细胞因子(肿瘤坏死因子-α和干扰素-γ)的分泌。此外,MMP25促进了核因子κB p65的核转位,表明核因子κB信号通路的激活可能介导了MMP25在TSCC中的促肿瘤功能。
本研究揭示了MMP25在TSCC中的新作用,突出了MMP25作为TSCC治疗靶点的潜力。