Casartelli G, Bonatti S, De Ferrari M, Scala M, Mereu P, Margarino G, Abbondandolo A
Mutagenesis Laboratory, National Cancer Institute-Genoa, Genoa, Italy.
Anal Quant Cytol Histol. 2000 Dec;22(6):486-92.
To assess the value of micronuclei in the characterization of precancerous lesions of the oral cavity with reference to their likelihood of progressing to malignant lesions.
The frequency of micronuclei was determined in exfoliated cells from normal oral mucosa, a preneoplastic condition (leukoplakia) and precancerous lesions with and without dysplasia, squamous cell carcinomas and sites of previous carcinomas that had been removed.
Average micronucleus frequencies were increased in precancerous lesions as compared to normal mucosa and further increased in carcinomas, suggesting that micronuclei are a biomarker of neoplastic progression in this type of cancer. With all samples, micronucleus frequencies were systematically higher when cells were collected by vigorous than by light scraping, suggesting a decreasing gradient from basal to superficial layers of mucosa. The micronucleus frequency did not vary with the sex or age of patients, while it did vary with the anatomic site of the lesions.
Although the gradual increase in micronucleus counts from normal mucosa to precancerous lesions to carcinomas suggests a link of this biomarker with neoplastic progression, the large overlapping of data prevents its use as a predictor of progression of precancerous lesions to malignancy in individual patients.
参照口腔癌前病变发展为恶性病变的可能性,评估微核在口腔癌前病变特征描述中的价值。
测定正常口腔黏膜、癌前状态(白斑)以及伴有或不伴有发育异常的癌前病变、鳞状细胞癌和已切除的既往癌部位的脱落细胞中的微核频率。
与正常黏膜相比,癌前病变中的平均微核频率增加,而在癌中进一步增加,这表明微核是这类癌症肿瘤进展的生物标志物。在所有样本中,通过用力刮取收集的细胞中的微核频率系统性地高于轻轻刮取的细胞,这表明从黏膜基底层到表层存在递减梯度。微核频率在患者性别或年龄方面无差异,但随病变的解剖部位而变化。
尽管从正常黏膜到癌前病变再到癌,微核计数逐渐增加表明该生物标志物与肿瘤进展有关,但数据的大量重叠使其无法作为个体患者癌前病变进展为恶性肿瘤的预测指标。