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中国人群中基因多态性与喉癌预后的关联

Association of genetic polymorphisms with laryngeal carcinoma prognosis in a Chinese population.

作者信息

Quan Fang, Zhang Feipeng, Bai Yanxia, Zhou Long, Yang Hua, Li Bin, Jin Tianbo, Li Huajing, Shao Yuan

机构信息

Department of Otolaryngology & Head Neck, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, 710061, China.

Sichuan Yanting Middle School, Mianyang, Sichuan, 621600, China.

出版信息

Oncotarget. 2017 Feb 7;8(6):10255-10263. doi: 10.18632/oncotarget.14381.

Abstract

We analyzed the effects of single-nucleotide polymorphisms (SNPs) on laryngeal carcinoma (LC) risk and overall survival (OS) in 170 Chinese male LC patients followed for 10 years. After assessment of clinical characteristics (age, laryngectomy, neck dissection, tumor differentiation, TNM status), the patients were genotyped for 24 SNPs associated with risk in multiple cancers. LC risk was assessed using log-rank test and Cox proportional hazard models. The median OS time was 48 months. By the follow-up deadline, OS was 41.2%. Kaplan-Meier analysis indicated 1-, 3-, and 5-year survival rates to be 84.7%, 57.2%, and 47.1%, respectively. Five LC clinicopathological characteristics, namely total laryngectomy (TL), low differentiation (LD), T3-T4, N1-N2, and clinical stage III-IV were associated with worse OS (HR: 2.35, p < 0.001; HR: 2.39, p = 0.02; HR: 2.17, p < 0.001; HR: 2.39, p < 0.001; and HR: 3.29, p < 0.001, respectively). Univariate cox regression analysis indicated that four SNPs were associated (p < 0.05) with LC OS in the codominant genetic model compared to patients with the homozygous wild-type genotype: rs10088262 G/A (HR = 1.57), rs1665650 A/G (HR = 0.65); rs3802842 C/C (HR = 2.18), and rs59336 T/A and T/T (HR = 0.61 and 2.61, respectively).

摘要

我们分析了单核苷酸多态性(SNP)对170例随访10年的中国男性喉癌(LC)患者的喉癌风险和总生存期(OS)的影响。在评估临床特征(年龄、喉切除术、颈部清扫术、肿瘤分化、TNM分期)后,对患者进行了与多种癌症风险相关的24个SNP的基因分型。使用对数秩检验和Cox比例风险模型评估LC风险。OS的中位时间为48个月。到随访截止时,OS为41.2%。Kaplan-Meier分析表明1年、3年和5年生存率分别为84.7%、57.2%和47.1%。五个LC临床病理特征,即全喉切除术(TL)、低分化(LD)、T3-T4、N1-N2和临床分期III-IV与较差的OS相关(HR:2.35,p<0.001;HR:2.39,p = 0.02;HR:2.17,p<0.001;HR:2.39,p<0.001;以及HR:3.29,p<0.001)。单因素Cox回归分析表明,与纯合野生型基因型患者相比,在共显性遗传模型中,有四个SNP与LC的OS相关(p<0.05):rs10088262 G/A(HR = 1.57)、rs1665650 A/G(HR = 0.65);rs3802842 C/C(HR = 2.18),以及rs59336 T/A和T/T(HR分别为0.61和2.61)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc6d/5354656/d2a5a5e6f13e/oncotarget-08-10255-g001.jpg

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