Chatrath P, Scott I S, Morris L S, Davies R J, Rushbrook S M, Bird K, Vowler S L, Grant J W, Saeed I T, Howard D, Laskey R A, Coleman N
MRC Cancer Cell Unit, Hutchison/MRC Research Centre, Hills Road, Cambridge CB2 2XZ, UK.
Br J Cancer. 2003 Sep 15;89(6):1048-54. doi: 10.1038/sj.bjc.6601234.
Histological classification of laryngeal epithelial lesions is highly subjective, and methods of cytological detection are not well developed. Improved determination of aberrant cell cycle entry may allow increased objectivity in histological assessment and enable the development of less invasive diagnostic cytology tests. Sections of normal larynx (n=10), laryngeal dysplasia (n=20) and laryngeal squamous cell carcinoma (SCC) (n=10) were classified according to the Ljubljana classification and stained for markers of cell cycle entry, minichromosome maintenance protein-2 (Mcm-2) and Ki67. Expression patterns were compared using double labelling confocal microscopy. There was a correlation between Mcm-2 and Ki67 labelling indices (rho=0.93; 95% CI [0.84, 0.97]) and both markers showed increased expression from normal epithelium to SCC (Mcm-2, P=0.001; Ki67, P=0.0002). Importantly, there was minimal expression of Mcm-2 or Ki67 in the most superficial layers of normal larynx and abnormal or atypical hyperplasia, in contrast to carcinoma in situ and SCC. Clusters of Mcm-2/5-positive cells were present in cytological preparations from SCC, but not from those showing atypical hyperplasia or inflammation in non-neoplastic tissue. Minichromosome maintenance protein-2 staining may increase the objectivity and reliability of histological grading of laryngeal epithelial lesions. Laryngeal brushings, combined with immuno-enhanced liquid-based cytology, could be useful, as a less invasive approach, to the detection of laryngeal malignant and premalignant lesions.
喉上皮病变的组织学分类主观性很强,而细胞学检测方法尚不完善。改进对异常细胞周期进入的判定可能会提高组织学评估的客观性,并有助于开发侵入性较小的诊断性细胞学检测方法。根据卢布尔雅那分类法对正常喉组织切片(n = 10)、喉发育异常组织切片(n = 20)和喉鳞状细胞癌(SCC)组织切片(n = 10)进行分类,并对细胞周期进入标记物、微小染色体维持蛋白-2(Mcm-2)和Ki67进行染色。使用双标记共聚焦显微镜比较表达模式。Mcm-2和Ki67标记指数之间存在相关性(rho = 0.93;95%可信区间[0.84, 0.97]),并且两种标记物从正常上皮到SCC均显示表达增加(Mcm-2,P = 0.001;Ki67,P = 0.0002)。重要的是,与原位癌和SCC相比,正常喉和异常或非典型增生的最表层中Mcm-2或Ki67的表达极少。SCC的细胞学制剂中存在Mcm-2/5阳性细胞簇,但非肿瘤组织中显示非典型增生或炎症的制剂中不存在。微小染色体维持蛋白-2染色可能会提高喉上皮病变组织学分级的客观性和可靠性。作为一种侵入性较小的方法,喉刷检联合免疫增强液基细胞学检查可能有助于检测喉恶性和癌前病变。