Jumonji domain containing 5 is a potential prognostic indicator in non-small cell lung cancer patients who received platinum-based chemotherapy

被引:4
作者
Xiang, Xueping [1 ]
Ma, Xiaojing [1 ]
Fang, Mao [2 ]
Zhong, Like [3 ]
Liu, Hui [1 ]
Liu, Hong [2 ]
Tong, Yinghui [3 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Dept Pathol, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Normal Univ Jinhua Peoples Hosp Joint Ct, 228 Xinhua St, Jinhua 321000, Zhejiang, Peoples R China
[3] Zhejiang Canc Hosp, Dept Pharm, Hangzhou 310022, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Jumonji domain containing 5 (JMJD5); prognosis; non-small cell lung cancer (NSCLC); platinum-based chemotherapy; survival outcome; H3K36ME2 HISTONE DEMETHYLASE; JMJD5; FUNCTIONS; PROLIFERATION; METASTASIS; STATISTICS; CARCINOMA; PROMOTES; CYCLE; KDM8; P53;
D O I
10.21037/tcr.2019.10.16
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Platinum-based chemotherapy is the cornerstone of non-small cell lung cancer (NSCLC) therapy. However, the molecular mechanisms and predictive markers of platinum chemoresistance have not been fully understood. Our recent study revealed that Jumonji domain containing 5 (JMJD5) expression in cells was elevated under DNA damage by alkylating agent or UV radiation, which suggests a potential role of JMJD5 in DNA damage related chemoresistance. However, the role of JMJD5 in NSCLC chemotherapy has not been reported. In this study, we demonstrated JMJD5 as a potential prognostic indicator in NSCLC patients who received platinum-based chemotherapy. Methods: JMJD5 protein expression level in tumor and adjacent normal tissues were detected by immunohistochemistry. Samples were from primary NSCLC patients who received platinum-based chemotherapy after surgical resection. Survival curves were presented by the Kaplan-Meier method and p value was acquired by log-rank test. Multivariate analysis was tested by Cox proportional-hazards regression method. Results: Elevated JMJD5 expression was found in 27.2% cases of tumor tissues (22/81), and high JMJD5 expression were significantly associated with poor overall survival time (OS) [HR =2.881 (1.774-9.121), P=0.001] and progression-free survival time (PFS) [HR =2.255 (1.417-5.886), P=0.004] in NSCLC patients who received platinum-based chemotherapy. In multivariate analyses, JMJD5 was proved to be an independent prognostic indictor for shorter OS [HR =2.339 (1.158-4.724), P=0.018] and PFS [HR =2.031 (1.095-3.767), P=0.025). Conclusions: High JMJD5 expression indicated a worse prognosis in NSCLC patients who received platinum-based chemotherapy, and JMJD5 may serve as a novel predictive marker in NSCLC chemotherapy.
引用
收藏
页码:2535 / 2542
页数:8
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