Ubiquitin D Promotes Progression of Oral Squamous Cell Carcinoma via NF-Kappa B Signaling

被引:13
|
作者
Song, An [1 ,2 ,3 ]
Wang, Yi [1 ,2 ,3 ]
Jiang, Feng [1 ,2 ,3 ]
Yan, Enshi [2 ,3 ]
Zhou, Junbo [4 ]
Ye, Jinhai [1 ,2 ,3 ]
Zhang, Hongchuang [5 ]
Ding, Xu [1 ,2 ]
Li, Gang [6 ]
Wu, Yunong [1 ,2 ,3 ]
Zheng, Yang [1 ,2 ,3 ]
Song, Xiaomeng [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Affiliated Stomatol Hosp, Dept Oral & Maxillofacial Surg, Nanjing 210000, Peoples R China
[2] Nanjing Med Univ, Jiangsu Prov Key Lab Oral Dis, Nanjing 210000, Peoples R China
[3] Jiangsu Prov Engn Res Ctr Stomatol Translat Med, Nanjing 210000, Peoples R China
[4] Nanjing Integrated Tradit Chinese & Western Med H, Dept Stomatol, Nanjing 210000, Peoples R China
[5] Xuzhou 1 Peoples Hosp, Dept Stomatol, Xuzhou 221000, Jiangsu, Peoples R China
[6] Xuzhou Med Univ, Affiliated Hosp, Dept Stomatol, Xuzhou 221000, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
epithelial-to-mesenchymal transition; NF-kappa B; oral squamous cell carcinoma; tumorigenesis; ubiquitin D; EPITHELIAL-MESENCHYMAL TRANSITION; PROTEIN FAT10 PROMOTES; INCREASED EXPRESSION; TUMOR-SUPPRESSOR; CANCER;
D O I
10.14348/molcells.2021.2229
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
Ubiquitin D (UBD) is highly upregulated in many cancers, and plays a pivotal role in the pathophysiological processes of cancers. However, its roles and underlying mechanisms in oral squamous cell carcinoma (OSCC) are still unclear. In the present study, we investigated the role of UBD in patients with OSCC. Quantitative real-time polymerase chain reaction and Western blot were used to measure the expression of UBD in OSCC tissues. Immunohistochemistry assay was used to detect the differential expressions of UBD in 244 OSCC patients and 32 cases of normal oral mucosae. In addition, CCK-8, colony formation, wound healing and Transwell assays were performed to evaluate the effect of UBD on the cell proliferation, migration, and invasion in OSCC, Furthermore, a xenograft tumor model was established to verify the role of UBD on tumor formation in vivo. We found that UBD was upregulated in human OSCC tissues and cell lines and was associated with clinical and pathological features of patients. Moreover, the overexpression of UBD promoted the proliferation, migration and invasion of OSCC cells; however, the knockdown of UBD exerted the opposite effects. In this study, our results also suggested that UBD promoted OSCC progression through NF-kappa B signaling. Our findings indicated that UBD played a critical role in OSCC and may serve as a prognostic biomarker and potential therapeutic target for OSCC treatment.
引用
收藏
页码:468 / 480
页数:13
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