AEBP1 is a negative regulator of skeletal muscle cell differentiation in oral squamous cell carcinoma

被引:0
|
作者
Okazaki, Fumika [1 ,2 ]
Yorozu, Akira [1 ,3 ,4 ]
Sekiguchi, Shohei [1 ,2 ]
Niinuma, Takeshi [1 ]
Maruyama, Reo [5 ]
Kitajima, Hiroshi [1 ]
Yamamoto, Eiichiro [1 ]
Ishiguro, Kazuya [1 ]
Toyota, Mutsumi [1 ]
Hatanaka, Yui [2 ]
Nishiyama, Koyo [2 ]
Ogi, Kazuhiro [2 ]
Kai, Masahiro [1 ]
Takano, Kenichi [4 ]
Ichimiya, Shingo [3 ]
Miyazaki, Akihiro [2 ]
Suzuki, Hiromu [1 ]
机构
[1] Sapporo Med Univ, Sch Med, Dept Mol Biol, S1, W17, Chuo Ku, Sapporo 0608556, Japan
[2] Sapporo Med Univ, Sch Med, Dept Oral Surg, Sapporo, Japan
[3] Sapporo Med Univ, Res Inst Immunol, Sch Med, Dept Human Immunol, Sapporo, Japan
[4] Sapporo Med Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Sapporo, Japan
[5] Japanese Fdn Canc Res, Canc Inst, Project Canc Epigen, Tokyo, Japan
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
基金
日本学术振兴会;
关键词
AEBP1; ACLP; OSCC; Myoblast; Muscle cell differentiation; CARBOXYPEPTIDASE-LIKE PROTEIN; ENHANCER-BINDING PROTEIN-1; GROWTH-FACTOR-BETA; LUNG;
D O I
10.1038/s41598-024-79061-3
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The tumor microenvironment plays a pivotal role in cancer development. We recently reported that in oral squamous cell carcinoma (OSCC), adipocyte enhancer-binding protein 1 (AEBP1) is abundantly expressed in cancer-associated fibroblasts (CAFs), leading to CAF activation and inhibition of CD8 + T cell infiltration. In the present study, we investigated whether AEBP1 contributes to the destruction and atrophy of muscle tissues in OSCC. By analyzing human skeletal muscle myoblasts (HSMMs), we found that AEBP1 is downregulated during muscle cell differentiation. Transcriptome analysis revealed that AEBP1 knockdown significantly upregulates myogenesis-related genes in HSMMs, and qRT-PCR and western blot analyses confirmed the induction of muscle-related genes, including MYOG, in HSMMs after AEBP1 knockdown. Conversely, ectopic expression of AEBP1 strongly suppressed myogenesis-related genes in HSMMs. Notably, indirect co-culture of HSMMs with OSCC cells led to AEBP1 upregulation and robust suppression of muscle-related genes in HSMMs. Treatment with TGF-beta 1 also upregulated AEBP1 and suppressed expression of muscle-related genes in HSMMs. Our findings suggest that AEBP1 is a negative regulator of skeletal muscle cell differentiation and that OSCC cells inhibit muscle cell differentiation, at least in part, by inducing AEBP1.
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页数:11
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