Lysophosphatidic acid induces integrin β6 expression in human oral squamous cell carcinomas cells via LPAR1 coupling to Gαi and downstream SMAD3 and ETS-1 activation

被引:14
作者
Xu, Mingyan [1 ,2 ]
Yin, Hao [3 ]
Cai, Yihuang [1 ,2 ]
Huang, Wenxia [1 ,2 ]
Ji, Qing [1 ,2 ]
Liu, Fan [3 ]
Shi, Songlin [3 ]
Deng, Xiaoling [3 ]
机构
[1] Fujian Univ Stomatol Biomat, Engn Res Ctr, Fuzhou, Fujian, Peoples R China
[2] Xiamen Med Coll, Affiliated Stomatol Hosp, Xiamen, Fujian, Peoples R China
[3] Xiamen Univ, Canc Res Ctr, Sch Med, Xiangan South Rd, Xiamen 361102, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Integrin beta-6; Lysophosphatidic acid; Oral cancer; Gene expression regulation; G protein coupled receptor; ALPHA-V-BETA-6; INTEGRIN; MESENCHYMAL TRANSITION; GROWTH-FACTOR; CANCER; RECEPTORS; FAMILY; PROLIFERATION; MIGRATION; OVARIAN;
D O I
10.1016/j.cellsig.2019.04.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Integrin beta 6 (ITGB6), an epithelial-specific integrin, is upregulated in oral squamous cell carcinomas (OSCC) and is associated with progression and metastasis of OSCC. Lysophosphatidic acid (LPA), an important bioactive phospholipid present in saliva, has also been related to OSCC cell migration and invasiveness. LPA exerts its biological effects through signal transduction pathways that ultimately regulate gene expression. However, it is unclear whether LPA signaling is involved in ITGB6 upregulation in OSCC. Therefore, the aim of the current study was to investigate the role of LPA in the regulation of ITGB6 expression in OSCC cells, and to delineate the molecular signaling pathways involved. Using SAS and HSC-3 OSCC cell lines, we found that LPA increases ITGB6 mRNA expression without affecting mRNA stability, suggesting that LPA acts by regulating ITGB6 gene transcription. In addition, we show that LPA stimulation increases phosphorylation and binding of the transcription factors SMAD3 and ETS-1 to the ITGB6 promoter resulting in ITGB6 active transcription. Finally, we demonstrate that LPA-induced ITGB6 expression is mediated via the LPA receptors 1 (LPAR1) coupling to G alpha(i). Our findings provide insights into the molecular mechanism underlying ITGB6 overexpression in OSCC and may have important implications for therapeutic purposes.
引用
收藏
页码:81 / 90
页数:10
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