Predictive single nucleotide polymorphism markers for acute oral mucositis in patients with nasopharyngeal carcinoma treated with radiotherapy

被引:17
|
作者
Le, Ziyu [1 ,3 ]
Niu, Xiaoshuang [1 ,3 ]
Chen, Ying
Ou, Xiaomin [1 ,3 ]
Zhao, Guoqi [4 ]
Liu, Qi [4 ]
Tu, Wenzhi [4 ]
Hu, Chaosu [1 ,3 ]
Kong, Lin [1 ,3 ]
Liu, Yong [2 ,3 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Dept Radiat Oncol, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Canc Ctr, Canc Res Inst, Shanghai 200032, Peoples R China
[3] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai 200032, Peoples R China
[4] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Dept Radiat Oncol, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金;
关键词
genetic polymorphism; nasopharyngeal carcinoma; radiotherapy; oral mucositis; ZNF24; PROGRESSION-FREE SURVIVAL; NORMAL TISSUE-REACTIONS; DSB REPAIR GENES; NF-KAPPA-B; NECK-CANCER; PHASE-III; CONCURRENT CHEMORADIOTHERAPY; HEPATOCELLULAR-CARCINOMA; CELL-PROLIFERATION; RADIATION-THERAPY;
D O I
10.18632/oncotarget.18450
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this study was to investigate the association between the susceptibility of severe oral mucositis (OM) in Chinese nasopharyngeal carcinoma (NPC) patients treated with radiotherapy and single nucleotide polymorphisms (SNPs) across the whole genome. SNPs were screened in a total of 24 patients with NPC and an additional 6 were subjected to mRNA expression analysis. Patients were subdivided into CTC 0-2 (CTC toxicity grade 0, 1, and 2) and CTC 3+ (CTC toxicity grade 3 and above) groups according to their CTC (common toxicity criteria) scores. The GTEx dataset was used to performed eQTL analyses and in-vitro functional assays were performed for eQTL-associated genes. Our data identified 7 functional SNPs associated with the development of OM. We observed that rs11081899-A, located in the 5'-UTR of the ZNF24 gene, was significantly correlated with a higher risk of severe mucositis (OR = 14.631, 95% CI = 2.61-105.46, p = 1.2 x 10(-4)), and positively associated with ZNF24 mRNA expression (p = 4.1 x 10(-6)) from GTEx dataset. In addition, high ZNF24 mRNA expression was associated with severe OM in patients with NPC (p = 0.02). Further functional assays revealed that ZNF24 knockdown reduced p65 expression and suppressed TNF-alpha-induced NF-kappa B activation and pro-inflammatory cytokines release. These findings suggested that rs11081899-A may be a genetic susceptibility factor for radiation-induced OM in patients with NPC, although its value in clinical application needs to be further verified in a large cohort. Also, we suggested that downregulation of ZNF24 may attenuate the development of mucositis by suppressing NF-kappa B activation.
引用
收藏
页码:63026 / 63037
页数:12
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