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Article type: Research Article
Authors: Yao, Ronga; 1 | Pu, Juanb; 1 | Fan, Ruihuaa | Zhu, Weiguoc | Ding, Xiaoronga | Shen, Xiaoyingd | Zhang, Tiechenga; *
Affiliations: [a] Departments of Oncology, Huaian First People’s Hospital, Nanjing Medical University, Huaian 223300, Jiangsu, China | [b] Department of Radiation Oncology, Lianshui People’s Hospital, Huaian 223300, Jiangsu, China | [c] Departments of Radiation Oncology, Huaian First People’s Hospital, Nanjing Medical University, Huaian 223300, Jiangsu, China | [d] Shanghai Outdo Biotech Co., Ltd., Shanghai 201399, China
Correspondence: [*] Corresponding auhtor: Tiecheng Zhang, Departments of Oncology, Huaian First People’s Hospital, Nanjing Medical University, Huaian 223300, Jiangsu, China. E-mail: [email protected].
Note: [1] Rong Yao and Juan Pu are co-first authors.
Abstract: Our study mainly investigated ubiquitin-specific protease 4 (USP4) expression in pathogenesis of esophageal cancer. The data showed significantly increased expression of USP4 in cancer tissues compared to that in para-carcinoma tissues (68.38% ± 25.60% vs 13.04% ± 9.95%, P= 0.000) and positive correlation between USP4 and pathology grade (r= 0.249, P= 0.014), although survival analysis revealed that USP4 expression was positively associated with the prognosis (32.4% vs 10.9%, P= 0.043). Grouped analysis revealed that the prognosis of patients with high USP4 expression were significantly better only in the small tumor subgroup (diameter ⩽ 5 cm) (52.6% VS 8.6%, P= 0.001) and the early stage subgroup (stages 1 and 2) (60.0% VS 16.7%, P= 0.006). Moreover, in the subgroup of clinical stages 1 and 2 with tumor diameter ⩽ 5 cm, high USP4 expression prolonged the survival time of esophageal cancer patients more significantly (75.5% VS 5.9%, P= 0.000). Based on these results, we speculated that it was possible to significantly improve the prognosis of patients with low USP4 expression by targeted therapy in early esophageal cancer. Taken together, our study uncovered a previously unknown function of USP4 in esophageal cancer and more investigations would be carried out to further study its regulation gene network and molecular biological mechanism in esophageal cancer.
Keywords: Tissue microarray, immunohistochemistry, USP4, esophageal cancer, prognosis
DOI: 10.3233/CBM-170308
Journal: Cancer Biomarkers, vol. 20, no. 3, pp. 317-323, 2017
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