EphA2 promotes the transcription of KLF4 to facilitate stemness in oral squamous cell carcinoma

被引:2
|
作者
Bai, Junqiang [1 ]
Chen, Yang [1 ,2 ]
Sun, Yunqing [1 ]
Wang, Xinmiao [1 ]
Wang, Yifan [1 ]
Guo, Shutian [1 ]
Shang, Zhengjun [1 ,3 ]
Shao, Zhe [1 ,4 ]
机构
[1] Wuhan Univ, Sch & Hosp Stomatolog, Key Lab Oral Biomed Minist Educ,Hubei Key Lab Stom, State Key Lab Oral & Maxillofacial Reconstruct & R, Wuhan, Peoples R China
[2] Wuhan Univ, Sch & Hosp Stomatol, Dept Oral & Maxillofacial Surg, Wuhan, Peoples R China
[3] Wuhan Univ, Sch & Hosp Stomatol, Dept Oral & Maxillofacial Head & Neck Oncol, Wuhan, Peoples R China
[4] Wuhan Univ, Sch & Hosp Stomatol, Day Surg Ctr, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
OSCC; Cancer stem cells; EphA2; KLF4; YAP; CANCER; DISRUPTION;
D O I
10.1007/s00018-024-05325-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ephrin receptor A2 (EphA2), a member of the Ephrin receptor family, is closely related to the progression of oral squamous cell carcinoma (OSCC). Cancer stem cells (CSCs) play essential roles in OSCC development and occurrence. The underlying mechanisms between EphA2 and CSCs, however, are not yet fully understood. Here, we found that EphA2 was overexpressed in OSCC tissues and was associated with poor prognosis. Knockdown of EphA2 dampened the CSC phenotype and the tumour-initiating frequency of OSCC cells. Crucially, the effects of EphA2 on the CSC phenotype relied on KLF4, a key transcription factor for CSCs. Mechanistically, EphA2 activated the ERK signalling pathway, promoting the nuclear translocation of YAP. Subsequently, YAP was bound to TEAD3, leading to the transcription of KLF4. Overall, our findings revealed that EphA2 can enhance the stemness of OSCC cells, and this study identified the EphA2/KLF4 axis as a potential target for treating OSCC.
引用
收藏
页数:16
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