参考文献/References:
[1]Torre LA,Bray F,Siegel RL,et al.Global cancer statistics,2012[J].CA Cancer J Clin,2015,65(2):87-108. [2]Dong J,Hu Z,Wu C,et al.Association analyses identify multiple new lung cancer susceptibility loci and their interactions with smoking in the Chinese population[J].Nat Genet,2012,44(8):895-899. [3]García Campelo MR,Alonso Curbera G,Aparicio Gallego G,et al.Stem cell and lung cancer development:blaming the Wnt,Hh and Notch signalling pathway[J].Clin Transl Oncol,2011,13(2):77-83. [4]Chen W,Zheng R,Baade PD,et al.Cancer statistics in China,2015[J].CA Cancer J Clin,2016,66(2):115-132. [5]Tonini G,D’Onofrio L,Dell’Aquila E,et al.New molecular insights in tobacco-induced lung cancer[J].Future Oncol,2013(9):649-655. [6]Wallis CJD,Satkunasivam R,Butaney M,et al.Association Between Smoking and Survival Benefit of Immunotherapy in Advanced Malignancies:A Systematic Review and Meta-Analysis[J].Am J Clin Oncol,2019,42(9):1. [7]Vaughan AE,Halbert CL,Wootton SK,et al.Lung cancer in mice induced by the jaagsiekte sheep retrovirus envelope protein is not maintained by rare cancer stem cells,but tumorigenicity does correlate with Wnt pathway activation[J].Mol Cancer Res,2012,10(1):86-95. [8]Schuller HM.Is cancer triggered by altered signalling of nicotinic acetylcholine receptors[J].Nat Rev Cancer,2009,9(3):195-205. [9]Kase S,Sugio K,Yamazaki K,et al.Expression of E-cadherin and beta-catenin in human non-small cell lung cancer and the clinical significance[J].Clin Cancer Res,2000,6(12):4789-4796. [10]Kurppa KJ,Denessiouk K,Johnson MS,et al.Activating ERBB4 mutations in non-small cell lung cancer[J].Oncogene,2016,35(10):1283-1291. [11]Tan X,Chen M.MYLK and MYL9 expression in non-small cell lung cancer identified by bioinformatics analysis of public expression data[J].Tumour Biol,2014,35(12):12189-12200. [12]Peifer M,Fernández-Cuesta L,Sos ML,et al.Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer[J].Nat Genet,2012,44(10):1104-1110. [13]Westhoff B,Colaluca IN,D’Ario G,et al.Alterations of the Notch pathway in lung cancer[J].Proc Natl Acad Sci USA,2009,106(52):22293-22298. [14]Fernandez-Cuesta L,Peifer M,Lu X,et al.Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids[J].Nat Commun,2014(5):3518.
相似文献/References:
[1]魏谭伟.先天性无虹膜症PAX6致病基因分析及其分子诊断研究[J].医学信息,2022,35(10):78.[doi:10.3969/j.issn.1006-1959.2022.10.019]
WEI Tan-wei.A PAX6 Pathogenic Gene Analysis and Molecular Diagnosis of Congenital Aniridia[J].Medical Information,2022,35(01):78.[doi:10.3969/j.issn.1006-1959.2022.10.019]
[2]吴玉斌,李先明.涎腺粘液表皮样癌与腺样囊性癌基因突变及靶向治疗研究[J].医学信息,2022,35(11):64.[doi:10.3969/j.issn.1006-1959.2022.11.018]
WU Yu-bin,LI Xian-ming.Study on Gene Mutation and Targeted Therapy of Mucoepidermoid Carcinoma and Adenoid Cystic Carcinoma of Salivary Gland[J].Medical Information,2022,35(01):64.[doi:10.3969/j.issn.1006-1959.2022.11.018]
[3]袁 康,谭 伟.多层螺旋CT用于小细胞肺癌与肺鳞癌的鉴别诊断价值分析[J].医学信息,2018,31(16):148.[doi:10.3969/j.issn.1006-1959.2018.16.047]
YUAN Kang,TAN Wei.Value of Multi-slice Spiral CT in Differential Diagnosis of Small Cell Lung Cancer and Lung Squamous Cell Carcinoma[J].Medical Information,2018,31(01):148.[doi:10.3969/j.issn.1006-1959.2018.16.047]
[4]符青云,欧阳小明,郅 程,等.结直肠癌组织EGFR、BRAF及NRAS基因突变检测及临床意义分析[J].医学信息,2022,35(13):83.[doi:10.3969/j.issn.1006-1959.2022.13.018]
FU Qing-yun,OUYANG Xiao-ming,ZHI Cheng,et al.Detection and Clinical Significance of EGFR, BRAF and NRAS Gene Mutations in Colorectal Cancer[J].Medical Information,2022,35(01):83.[doi:10.3969/j.issn.1006-1959.2022.13.018]
[5]徐园园,毛荣军,曾 敏,等.软骨母细胞瘤样骨肉瘤穿刺标本免疫组化H3F3B、IMP3、Clusterin联合H3F3B基因突变检测的意义[J].医学信息,2022,35(17):60.[doi:10.3969/j.issn.1006-1959.2022.17.014]
XU Yuan-yuan,MAO Rong-jun,ZENG Min,et al.Significance of Immunohistochemical Detection of H3F3B, IMP3, Clusterin and H3F3B Gene Mutation in Puncture Specimens of Chondroblastoma-like Osteosarcoma[J].Medical Information,2022,35(01):60.[doi:10.3969/j.issn.1006-1959.2022.17.014]
[6]周 莛,朱 岷.儿童肾上腺危象临床特征及基因分析[J].医学信息,2020,33(09):67.[doi:10.3969/j.issn.1006-1959.2020.09.020]
ZHOU Ting,ZHU Min.Clinical Characteristics and Genetic Analysis of Children’s Adrenal Crisis[J].Medical Information,2020,33(01):67.[doi:10.3969/j.issn.1006-1959.2020.09.020]
[7]吴 思,邢巍巍.辽西地区非综合征性耳聋患者及其亲属常见耳聋基因检测结果分析[J].医学信息,2020,33(11):122.[doi:10.3969/j.issn.1006-1959.2020.11.038]
WU Si,XING Wei-wei.Analysis of Common Deafness Gene Detection Results in Non-syndromic Deafness Patients and Their Relatives in Western Liaoning[J].Medical Information,2020,33(01):122.[doi:10.3969/j.issn.1006-1959.2020.11.038]
[8]谌玉佳,杨江涛,庄利明,等.深圳市光明区新生儿耳聋基因筛查结果分析[J].医学信息,2020,33(13):134.[doi:10.3969/j.issn.1006-1959.2020.13.039]
CHEN Yu-jia,YANG Jiang-tao,ZHUANG Li-ming,et al.Analysis of Genetic Screening Results of Newborn Deafness in Guangming District,Shenzhen[J].Medical Information,2020,33(01):134.[doi:10.3969/j.issn.1006-1959.2020.13.039]
[9]何小鹏,高 亭.盐酸安罗替尼一线联合化疗后序贯盐酸安罗替尼治疗广泛期小细胞肺癌的效果[J].医学信息,2022,35(23):76.[doi:10.3969/j.issn.1006-1959.2022.23.012]
HE Xiao-peng,GAO Ting.Effect of Sequential Anlotinib Hydrochloride After First-line Combined Chemotherapy on Extensive Stage Small Cell Lung Cancer[J].Medical Information,2022,35(01):76.[doi:10.3969/j.issn.1006-1959.2022.23.012]
[10]郑 珊,刘雪静,田秀英.MTM1基因突变致新生儿中央核性肌病2例[J].医学信息,2021,34(06):191.[doi:10.3969/j.issn.1006-1959.2021.06.054]