Kersting M, Friedl C, Kraus A, Behn M, Pankow W, Schuermann M
Klinikum der Philipps-Universität, Zentrum für Innere Medizin, Abteilung Hämatologie/Onkologie/Immunologie, Marburg, Germany.
J Clin Oncol. 2000 Sep 15;18(18):3221-9. doi: 10.1200/JCO.2000.18.18.3221.
The aim of this study was to investigate the frequency of three (epi)genetic alterations (p53 and K-ras mutations and p16(INK4a) promoter hypermethylation) in symptomatic chronic smokers compared with patients with lung cancer and to evaluate the use of exfoliative material for such analyses.
Fifty-one patients with histologically confirmed lung cancer and 25 chronic smokers (> 20 pack-years) were investigated for mutations in the K-ras (codon 12) and p53 (codons 248, 249, and 273) genes and for allelic hypermethylation of the p16(INK4a) gene. DNA was isolated from sputum and bilateral bronchial lavage, and brushings were taken at bronchoscopy.
Forty-one genetic lesions were detected within exfoliative material from the group of 51 patients with lung cancer and 10 lesions in the chronic smoker group. K-ras mutations occurred exclusively in the lung cancer group, whereas p53 mutations and p16(INK4a) promoter hypermethylation were also found in chronic smokers. Three of eight chronic smokers who harbored an (epi)genetic alteration were subsequently diagnosed with lung cancer. Analysis of sputum yielded information equivalent to that of samples obtained during bronchoscopy.
p16(INK4a) promoter hypermethylation and p53 mutations can occur in chronic smokers before any clinical evidence of neoplasia and may be indicative of an increased risk of developing lung cancer or of early disease. K-ras mutations occur exclusively in the presence of clinically detectable neoplastic transformation. Molecular analysis of sputum for such markers may provide an effective means of screening chronic smokers to enable earlier detection and therapeutic intervention of lung cancer.
本研究旨在调查有症状的慢性吸烟者与肺癌患者相比,三种(表观)遗传改变(p53和K-ras基因突变以及p16(INK4a)启动子高甲基化)的发生频率,并评估用于此类分析的脱落物质的实用性。
对51例经组织学确诊的肺癌患者和25例慢性吸烟者(吸烟量>20包年)进行K-ras(密码子12)和p53(密码子248、249和273)基因的突变以及p16(INK4a)基因的等位基因高甲基化检测。从痰液和双侧支气管灌洗中分离DNA,并在支气管镜检查时进行刷检。
在51例肺癌患者组的脱落物质中检测到41个遗传损伤,在慢性吸烟者组中检测到10个损伤。K-ras基因突变仅发生在肺癌组,而p53基因突变和p16(INK4a)启动子高甲基化在慢性吸烟者中也有发现。8例有(表观)遗传改变的慢性吸烟者中有3例随后被诊断为肺癌。痰液分析得到的信息与支气管镜检查时获得的样本相当。
在肿瘤形成的任何临床证据出现之前,p16(INK4a)启动子高甲基化和p53基因突变可能发生在慢性吸烟者中,可能表明患肺癌或早期疾病的风险增加。K-ras基因突变仅在临床可检测到的肿瘤转化存在时发生。对痰液进行此类标志物的分子分析可能提供一种有效的手段来筛查慢性吸烟者,以便更早地检测和干预肺癌。