Metformin disrupts malignant behavior of oral squamous cell carcinoma via a novel signaling involving Late SV40 factor/Aurora-A

被引:16
作者
Chen, Chang-Han [1 ,2 ,3 ,4 ]
Tsai, Hsin-Ting [1 ,5 ,6 ]
Chuang, Hui-Ching [5 ,6 ,8 ]
Shiu, Li-Yen [7 ]
Su, Li-Jen [9 ]
Chiu, Tai-Jan [10 ]
Luo, Sheng-Dean [5 ,6 ]
Fang, Fu-Min [6 ,11 ]
Huang, Chao-Cheng [6 ,12 ]
Chien, Chih-Yen [5 ,6 ]
机构
[1] Kaohsiung Chang Gung Mem Hosp, Inst Translat Res Biomed, Kaohsiung, Taiwan
[2] Natl Chi Nan Univ, Dept Appl Chem, Nantou, Taiwan
[3] Natl Chi Nan Univ, Grad Inst Biomed & Biomed Technol, Nantou, Taiwan
[4] Kaohsiung Med Univ, Ctr Infect Dis & Canc Res, Kaohsiung, Taiwan
[5] Kaohsiung Chang Gung Mem Hosp, Dept Otolaryngol, Kaohsiung, Taiwan
[6] Chang Gung Univ, Coll Med, Kaohsiung, Taiwan
[7] I SHOW Univ, E Da Hosp, Dept Med Res, Kaohsiung, Taiwan
[8] E Da Canc Hosp, Cell Therapy & Res Ctr, Dept Med Res, Kaohsiung, Taiwan
[9] Natl Cent Univ, Grad Inst Syst Biol & Bioinformat, Jhongli, Taiwan
[10] Chang Gung Univ, Coll Med, Dept Hematol Oncol, Kaohsiung, Taiwan
[11] Kaohsiung Chang Gung Mem Hosp, Dept Radiat Oncol, Kaohsiung, Taiwan
[12] Kaohsiung Chang Gung Mem Hosp, Dept Pathol, Kaohsiung, Taiwan
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
ACTIVATED PROTEIN-KINASE; TRANSCRIPTION FACTOR LSF; AURORA-A; IN-VITRO; POOR-PROGNOSIS; TUMOR PROGRESSION; CANCER-CELLS; CYCLE ARREST; HEAD; OVEREXPRESSION;
D O I
10.1038/s41598-017-01353-8
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
Conventional therapeutic processes in patient with OSCC are associated with several unfavorable effects leading to patients with poor survival rate. Metformin has been shown to protect against a variety of specific diseases, including cancer. However, the precise roles and mechanisms underlying the therapeutic effects of metformin on OSCC remain elusive. In the current study, in vitro and xenograft model experiments revealed that metformin inhibited growth and metastasis of oral cancer cells. Importantly, metformin-restrained tumorigenesis of oral cancer was accompanied with strong decrease of both Aurora-A and Late SV40 Factor (LSF) expressions. Furthermore, LSF contributed to Aurora-A-elicited malignancy behaviors of oral cancer via binding to the promoter region of Aurora-A. A significant correlation was observed between LSF and Aurora-A levels in a cohort of specimens of oral cancer. These findings showed that a novel LSF/Aurora-A-signaling inhibition supports the rationale of using metformin as potential OSCC therapeutics.
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页数:15
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