Feller L, Lemmer J
Department of Periodontology and Oral Medicine, University of Limpopo, Medunsa Campus, South Africa.
Int J Dent. 2011;2011:321750. doi: 10.1155/2011/321750. Epub 2011 Oct 5.
Potentially malignant oral leukoplakias arise within precancerized epithelial fields consisting of cytogenetically altered keratinocytes at various stages of transformation. The evolution of a clone of keratinocytes culminating in a precancerous phenotype is a function of the number of mutagenic events, rather than the sequential order in which they occur. The altered molecular configurations of the transformed precancerous keratinocytes may confer upon them a growth advantage in relation to the unaltered neighbouring keratinocytes. Replicative clonal expansion of these keratinocytes results in the progressive replacement of the surrounding normal keratinocytes by the fitter clone or clones of altered cells. The precancerized oral epithelial field may have a clinically normal appearance and microscopically may be normal or may show dysplasia. Oral leukoplakias arising within a precancerized epithelial field in which the keratinocytes show DNA aneuploidy or loss of heterozygosity at certain specific chromosomal loci have the potential to progress to carcinoma. The pathogenic mechanisms that drive the carcinomatous transformation of oral leukoplakias, in which cytogenetic alterations in the keratinocytes cannot be detected, are unknown.
潜在恶性口腔白斑出现在癌前上皮区域内,该区域由处于不同转化阶段的细胞遗传学改变的角质形成细胞组成。角质形成细胞克隆的进化最终导致癌前表型,这是诱变事件数量的函数,而不是它们发生的顺序。转化的癌前角质形成细胞改变的分子构型可能使其相对于未改变的相邻角质形成细胞具有生长优势。这些角质形成细胞的复制性克隆扩增导致更适应的一个或多个改变细胞克隆逐渐取代周围的正常角质形成细胞。癌前口腔上皮区域在临床上可能外观正常,显微镜下可能正常或可能显示发育异常。在癌前上皮区域内出现的口腔白斑,其中角质形成细胞在某些特定染色体位点显示DNA非整倍体或杂合性缺失,有可能发展为癌。驱动口腔白斑发生癌变转化的致病机制尚不清楚,在这些白斑中无法检测到角质形成细胞的细胞遗传学改变。