TFIIB-related factor 2 regulates glucose-regulated protein 78 expression in acquired middle ear cholesteatoma

被引:1
|
作者
Sui, RongCui [1 ,2 ]
Liu, ChengCheng [3 ,4 ]
Wang, Na [1 ,2 ]
Fan, XinTai [1 ,2 ]
Han, ShuHui [1 ,2 ]
Zhang, Jie [1 ,2 ]
Hou, LingXiao [1 ,2 ]
Zhang, XianZhao [5 ]
Xu, AnTing [1 ,2 ]
机构
[1] Shandong Univ, Hosp 2, Cheeloo Coll Med, Dept Otolaryngol, 274 Beiyuan Rd, Jinan, Shandong, Peoples R China
[2] Shandong Univ, Hosp 2, Cheeloo Coll Med, Natl Hlth Commiss,Key Lab Otolaryngol, 274 Beiyuan Rd, Jinan, Shandong, Peoples R China
[3] Shandong First Med Univ, Hearing Reconstruct Key Lab Shandong Prov, Cent Lab, Shandong Prov Hosp, 324 Jingwu Weiqi Rd, Jinan, Shandong, Peoples R China
[4] Shandong Univ, Inst Med Sci, Hosp 2, 274 Beiyuan Rd, Jinan, Shandong, Peoples R China
[5] First Peoples Hosp Jining, Dept Otolaryngol, 6 Hlth Rd, Jining, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
BRF2; GRP78; Acquired middle ear cholesteatoma; ENDOPLASMIC-RETICULUM STRESS; ER STRESS; GRP78; CANCER; CELL; PROLIFERATION; PATHOGENESIS; APOPTOSIS; AMPLICON; 8P11-12;
D O I
10.1016/j.bbrc.2020.12.052
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
Acquired middle ear cholesteatoma leads to hearing loss, ear discharge, ear pain, and more serious intracranial complications. However, there is still no effective treatment other than surgery. TFIIB-related factor 2 (BRF2) acted as a redox sensor overexpressing in oxidative stress which linked endoplasmic reticulum (ER) stress, while glucose-regulated protein 78 (GRP78) was a biomarker of ER stress in cancer, atherosclerosis and inflammation. In our study, we investigated the roles of BRF2 and GRP78 in acquired middle ear cholesteatoma. Our results revealed that the expression of BRF2 was significant increased in acquired middle ear cholesteatoma, and which was positively correlated with the expression of GRP78. In addition, BRF2 and GRP78 showed colocalization in epithelium of acquired middle ear cholesteatomas and HaCaT cells. Prolongation of LPS stimulation in HaCaT cells escalated the expression of BRF2 and GRP78. To confirm the role of BRF2 and GRP78, we transfected si-BRF2 into HaCaT cells. All results indicated that BRF2 expression positively regulates the expression of GRP78 and may participate in the pathogenesis of acquire middle ear cholesteatoma. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:95 / 100
页数:6
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