癌症研究
CEBPA公司
车站3
细胞周期
细胞迁移
生物
转录因子
STAT蛋白
癌基因
细胞凋亡
细胞
信号转导
细胞生物学
生物化学
基因
遗传学
作者
Minhui Zhu,Yi Ma,Wei Wang,Meng Li,Shicai Chen,Fei Liu,Xiaoqiong Shi,Hongsen Bi,Chen Zhang,Fangfei Nie,Hongliang Zheng,Caiyun Zhang
标识
DOI:10.1158/1541-7786.mcr-23-0038
摘要
Abstract Tongue squamous cell carcinoma (TSCC) is the main pathologic subtype of oral cancer, and the current therapeutic effect is far from satisfactory. The signal peptide-CUB-EGF domain-containing protein 3 (SCUBE3) has been shown to be a tumor-promoting factor in several malignancies. However, little is known about the role of SCUBE3 in TSCC. In this study, we identified that SCUBE3 was highly expressed in TSCC. Clinically, high expression of SCUBE3 was positively associated with tumor stage and T stage of TSCC. Functionally, SCUBE3 silence remarkably restrained cell proliferation, migration, and invasion, induced apoptosis as well as cell cycle arrest in G2-phase, and weakened the tumorigenicity of TSCC cells in vivo. Mechanistically, SCUBE3 promoted the direct binding of CCAAT enhancer binding protein alpha (CEBPA) to C-C motif chemokine ligand 2 (CCL2) promoter in TSCC cells. Interestingly, CCL2 overexpression partially reversed the inhibitory effect of SCUBE3 deficiency on TSCC cell viability and migration. Moreover, STAT3 signaling contributed to CCL2-mediated phenotypes in TSCC cells. Implications: Our data revealed a tumor-promoting role for SCUBE3 in TSCC via the CEBPA/CCL2/STAT3 axis, which provided new insight into novel potential therapeutic target for TSCC.
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