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논문 기본 정보

자료유형
학술저널
저자정보
Xiaomeng Song (The Affiliated Stomatological Hospital of Nanjing Medical University) An Song (The Affiliated Stomatological Hospital of Nanjing Medical University) Yi Wang (The Affiliated Stomatological Hospital of Nanjing Medical University) Feng Jiang (Nanjing Medical University) Enshi Yan (Nanjing Medical University) Junbo Zhou (Department of Stomatology Nanjing Integrated Traditional Chinese and Western Medicine Hospital) Jinhai Ye (Nanjing Medical University) Hongchuang Zhang (Department of Stomatology Xuzhou No. 1 Peoples Hospital) Xu Ding (Nanjing Medical University) Gang Li (Affiliated Hospital of Xuzhou Medical University) Yunong Wu (The Affiliated Stomatological Hospital of Nanjing Medical University) Yang Zheng (The Affiliated Stomatological Hospital of Nanjing Medical University)
저널정보
한국분자세포생물학회 Molecules and Cells Molecules and Cells 제44권 제7호
발행연도
2021.1
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468 - 480 (13page)

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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-κB 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.

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