CDKN3 expression is an independent prognostic factor and associated with advanced tumor stage in nasopharyngeal carcinoma

被引:19
作者
Chang, Shih-Lun [1 ,2 ]
Chen, Tzu-Ju [2 ,3 ]
Lee, Ying-En [4 ,5 ]
Lee, Sung-Wei [6 ]
Lin, Li-Ching [6 ]
He, Hong-Lin [3 ]
机构
[1] Chi Mei Med Ctr, Dept Otolaryngol, Tainan, Taiwan
[2] Chung Hwa Univ Med Technol, Dept Optometry, Tainan, Taiwan
[3] Chi Mei Med Ctr, Dept Pathol, Tainan, Taiwan
[4] Kaohsiung Chang Gung Mem Hosp, Dept Anesthesiol, Kaohsiung, Taiwan
[5] Chang Gung Univ, Coll Med, Kaohsiung, Taiwan
[6] Chi Mei Med Ctr, Dept Radiat Oncol, Tainan, Taiwan
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2018年 / 15卷 / 10期
关键词
CDKN3; nasopharyngeal carcinoma; NPC; cell cycle; transcriptome; KINASE INHIBITOR 3; CELL-PROLIFERATION; PHOSPHATASE; XIAP; SURVIVAL; KAP;
D O I
10.7150/ijms.25065
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Through data mining from the public transcriptome of NPC, cyclin-dependent kinase inhibitor 3 (CDKN3) was identified as a significantly upregulated gene in NPC. CDKN3 functions as a key factor in cell cycle regulation. This study was aimed to investigate the expression of CDKN3 in NPC tissues and its prognostic significance. Methods: Immunohistochemistry was performed for 124 NPC patients to assess the protein expression of CDKN3. The stainings of CDKN3 were scored by using H-score method. The relationships between CDKN3 expression status and clinicopathological parameters, disease-specific survival (DSS), distant metastasis-free survival (DMeFS), and local recurrence-free survival (LRFS) were statistically analyzed. Results: High expression of CDKN3 was significantly associated with higher primary nodal status (P=0.030) and higher TNM stage (P=0.019). In univariate analysis, high expression of CDKN3 predicted worse DSS (P<0.0001), DMeFS (P<0.0001), and LRFS (P<0.0001). In multivariate analysis, CDKN3 overexpression still acted as an independent prognostic factor for worse DSS (P<0.001; hazard ratio [HR]=11.999, 95% CI: 5.378-26.771), DMeFS (P<0.001; HR=15.069, 95% CI: 5.884-38.592), and LRFS (P<0.001; HR=5.000, 95% CI: 2.312-10.815). Conclusion: High expression of CDKN3 was an independent negative prognostic factor for NPC and was associated with advanced disease status. It might serve as potential therapeutic target and aid in risk stratification for patients with NPC.
引用
收藏
页码:992 / 998
页数:7
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