[1]张 令,王 宁,许 楠,等.核苷酸剪切修复基因mRNA和蛋白对头颈部鳞状细胞癌发生的预测价值研究[J].陕西医学杂志,2023,52(12):1680-1683.[doi:DOI:10.3969/j.issn.1000-7377.2023.12.011]
 ZHANG Ling,WANG Ning,XU Nan,et al.Predictive value of mRNA and protein of NER genes for occurrence of head and neck squamous cell carcinoma[J].,2023,52(12):1680-1683.[doi:DOI:10.3969/j.issn.1000-7377.2023.12.011]
点击复制

核苷酸剪切修复基因mRNA和蛋白对头颈部鳞状细胞癌发生的预测价值研究
分享到:

《陕西医学杂志》[ISSN:1000-7377/CN:61-1281/TN]

卷:
52
期数:
2023年12期
页码:
1680-1683
栏目:
临床研究
出版日期:
2023-12-05

文章信息/Info

Title:
Predictive value of mRNA and protein of NER genes for occurrence of head and neck squamous cell carcinoma
作者:
张 令12王 宁3许 楠4张晓彤1韩 鹏1
(1.西安交通大学第一附属医院耳鼻咽喉头颈外科,陕西 西安 710061; 2.西安交通大学第二附属医院耳鼻咽喉头颈外科,陕西 西安 710004; 3.神木市医院耳鼻喉科,陕西 神木 719300; 4.西安市鄠邑区人民医院耳鼻喉科,陕西 西安 710300)
Author(s):
ZHANG LingWANG NingXU NanZHANG XiaotongHAN Peng
(Department of Otorhinolaryngology Head and Neck Surgery,First Affiliated Hospital of Xi'an Jiaotong University,Xi'an 710061,China)
关键词:
头颈部鳞状细胞癌 核苷酸剪切修复基因 核苷酸剪切修复蛋白 影响因素 预测价值
Keywords:
Head and neck squamous cell carcinoma Nucleotide excision repair genes Nucleotide excision repair protein Influencing factors Predictive value
分类号:
R 739.91
DOI:
DOI:10.3969/j.issn.1000-7377.2023.12.011
文献标志码:
A
摘要:
目的:探讨核苷酸剪切修复(NER)基因mRNA和蛋白对头颈部鳞状细胞癌(HNSCC)发生的预测价值。方法:选取HNSCC患者98例为病例组,选取18岁及以上健康人群95例为对照组。采用荧光定量PCR实验和反相蛋白微阵列(RPPA)实验检测两组外周血淋巴细胞中9个核心NER基因mRNA和蛋白表达水平。采用Logistic回归分析HNSCC发生的影响因素。绘制受试者工作特征(ROC)曲线分析NER基因mRNA和蛋白表达对HNSCC发生的预测价值。结果:与对照组比较,病例组XPA mRNA和蛋白表达降低,XPB mRNA表达降低(均P<0.05)。XPA mRNA≤19.85和XPA蛋白<0.206是HNSCC发生的独立危险因素(均P<0.05)。单独XPA蛋白、XPA mRNA以及两者联合预测HNSCC发生的曲线下面积(AUC)分别为0.637、0.592、0.674,两者联合的AUC大于单项AUC(均P<0.05)。结论:XPA mRNA和蛋白表达水平是HNSCC发生的影响因素,XPA mRNA和蛋白联合预测HNSCC的发生较两者单独预测的价值更高。
Abstract:
Objective:To investigate the predictive value of mRNA and protein of nucleotide excision repair(NER)genes for occurrence of head and neck squamous cell carcinoma(HNSCC).Methods:A total of 98 HNSCC patients were selected as the case group,and 95 healthy people aged 18 years and over were selected as the control group.PCR and RPPA were used to detect the mRNA and protein expression levels of 9 core NER genes in peripheral blood lymphocytes of the two groups.Correlation of NER gene mRNA and protein expression level was analyzed by Spearman method.Logistic regression was used to analyze the influencing factors of HNSCC.ROC curve was drawn to analyze the predictive value of NER gene mRNA and protein expression for HNSCC.Results:Compared with the control group,the mRNA and protein expression of XPA and the mRNA expression of XPB were decreased in the case group(all P<0.05).XPA mRNA≤19.85 and XPA protein <0.206 were independent risk factors for HNSCC(both P<0.05).The AUC of XPA protein,XPA mRNA and their combination for predicting HNSCC were 0.637,0.592 and 0.674,respectively.The AUC of the combination of XPA protein and XPA mRNA was greater than that of each single item(all P<0.05).Conclusion:The expression levels of XPA mRNA and protein are risk factors for the occurrence of HNSCC.The combination of XPA mRNA and protein has a higher predictive value for the occurrence of HNSCC than either one alone.

参考文献/References:

[1] Auperin A.Epidemiology of head and neck cancers:An update[J].Curr Opin Oncol,2020,32(6):178-186.
[2] 郭武辉,袁 倩.早期喉癌患者血清膜联蛋白A2、环氧合酶-2及色素框同源物7检测及意义[J].陕西医学杂志,2021,50(11):1446-1448.
[3] 张 驰,杜锦朵,赵 雷,等.RECK、MMP-14及VEGF在喉癌组织中的表达及临床意义[J].陕西医学杂志,2015,44(3):281-283.
[4] 屈 慧,皇 海,张 蕊.血清细胞角蛋白18、骨桥蛋白水平与原发性喉癌患者临床分期相关性研究[J].陕西医学杂志,2021,50(11):1452-1456.
[5] Zhang X,Yin M,Hu J.Nucleotide excision repair:A versatile and smart toolkit[J].Acta Biochim Biophys Sin(Shanghai),2022,54(4):807-819.
[6] Wu HC,Kehm R,Santella RM,et al.DNA repair phenotype and cancer risk:A systematic review and meta-analysis of 55 case-control studies[J].Sci Rep,2022,12(8):3405.
[7] Chatterjee N,Walker GC.Mechanisms of DNA damage,repair,and mutagenesis[J].Environ Mol Mutagen,2017,58(6):235-263.
[8] Pasqui A,Boddi A,Canpanacci DA,et al.Alteration of the nucleotide excision repair(NER)pathway in soft tissue sarcoma[J].Int J Mol Sci,2022,23(2):85-87.
[9] Spicak G.Nucleotide excision repair in humans[J].DNA Repair(Amst),2015,36(5):13-18.
[10] Apostolou Z,Chatzinikolaou G,Stratigi K,et al.Nucleotide excision repair and transcription-associated genome instability[J].Bioessays,2019,41(4):e1800201.
[11] Sancar A.Mechanisms of DNA repair by photolyase and excision nuclease(Nobel Lecture)[J].Angew Chem Int Ed Engl,2016,55(30):8502-8527.
[12] Merolla F,Mascolo M,Ilardi G,et al.Nucleotide excision repair and head and neck cancers[J].Front Biosci(Landmark Ed),2016,21(3):55-69.
[13] Souza A,Blee AM,Chazin WJ.Mechanism of action of nucleotide excision repair machinery[J].Biochem Soc Trans,2022,50(1):375-386.
[14] Han P,Gao F,Liu H,et al.Reduced mRNA expression of nucleotide excision repair genes in lymphocytes and risk of squamous cell carcinoma of the head and neck[J].Carcinogenesis,2017,38(1):504-510.
[15] Ren P,Niu X,Liu C,et al.Associations between expression levels of nine core nucleotide excision repair genes in lymphocytes and risk of head and neck squamous cell carcinomas in a Chinese population[J].Int J Clin Oncol,2020,25(2):660-669.
[16] Wang LE,Hu Z,Stugis EM,et al.Reduced DNA repair capacity for removing tobacco carcinogen-induced DNA adducts contributes to risk of head and neck cancer but not tumor characteristics[J].Clin Cancer Res,2010,16(5):764-774.
[17] Wei Q,Wang LE,Stugis EM,et al.Expression of nucleotide excision repair proteins in lymphocytes as a marker of susceptibility to squamous cell carcinomas of the head and neck[J].Cancer Epidemiol Biomarkers Prev,2005,14(2):1961-1966.
[18] Wu L,Gao X,Ye D,et al.Association of the XPA A23G polymorphism with the risk of head and neck carcinomas:Evidence from 5491 subjects[J].Mol Clin Oncol,2015,3(5):649-654.
[19] Liu J,Zhang Z,Cao XL,et al.XPA A23G polymorphism and susceptibility to cancer:A meta-analysis[J].Mol Biol Rep,2012,39(1):6791-6799.
[20] Lu B,Li J,Gao Q,et al.Laryngeal cancer risk and common single nucleotide polymorphisms in nucleotide excision repair pathway genes ERCC1,ERCC2,ERCC3,ERCC4,ERCC5 and XPA[J].Gene,2014,542(1):64-68.

相似文献/References:

[1]张 令,敬 怡,刘 琪,等.整合DNA修复能力与核苷酸剪切修复标志物评估头颈鳞癌发病风险的初步研究[J].陕西医学杂志,2023,52(11):1502.[doi:DOI:10.3969/j.issn.1000-7377.2023.11.011]

备注/Memo

备注/Memo:
基金项目:陕西省自然科学基础研究计划面上项目(2023-JC-YB-791); 西安交通大学第一附属医院基金资助项目(2021ZYTS-02)
更新日期/Last Update: 2023-12-05