Elevated RUNX1 is a prognostic biomarker for human head and neck squamous cell carcinoma

Author:

Feng Xiaodong1ORCID,Zheng Zhiwei2,Wang Yi1,Song Guanghui1,Wang Lu3,Zhang Zhijun4,Zhao Jinxia1,Wang Qing1,Lun Limin1

Affiliation:

1. Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao 266000, China

2. Department of Oral and Maxillofacial-Head and Neck Oncology, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China

3. Department of Education and Training, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao 266000, China

4. Department of Clinical Laboratory, Taian City Central Hospital, Taian 271000, China

Abstract

Runt-related transcription factors regulate many developmental processes such as proliferation and differentiation. In this study, the function of the runt-related transcription factor 1 (RUNX1) was investigated in head and neck squamous cell carcinoma (HNSCC). Our results show that RUNX1 expression was elevated in HNSCC patients, which was greatly correlated with the N stage, tumor size, and American Joint Committee on Cancer stage. Cox proportional hazard models showed that RUNX1 could be used as a prognostic indicator for the overall survival of HNSCC patients (hazard ratio, 5.572; 95% confidence interval, 1.860–9.963; P <  0.001). Moreover, suppression of RUNX1 inhibited HNSCC cell proliferation, migration, and invasion. Using the HNSCC xenograft nude mouse model, we found that the shRUNX1-transfected tumor (sh-RUNX1) was significantly smaller both in size and weight than the control vector-transfected tumor (sh-Control). In conclusion, our results show that the elevated RUNX1 expression was correlated with tumor growth and metastasis in HNSCC, indicating that RUNX1 could be used as a biomarker for tumor recurrence and prognosis.

Funder

Affiliated Hospital of Qingdao University Outstanding Young Scientists Foundation

China Postdoctoral Science Foundation

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

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