Accurso Brent T, Warner Blake M, Knobloch Thomas J, Weghorst Christopher M, Shumway Brian S, Allen Carl M, Kalmar John R
The Ohio State University College of Dentistry, Columbus, OH 43210, USA.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2011 Sep;112(3):359-66. doi: 10.1016/j.tripleo.2011.03.042. Epub 2011 Jul 20.
OLP is a relatively common immune-mediated mucosal condition with a predilection for middle-aged women. Although classified as a premalignant condition, this classification remains controversial. Using stringent diagnostic criteria, some authors have found that OLP patients are not at increased risk for oral SCC. Credible but limited genetic evidence also indicates that epithelial tissues from OLP patients diagnosed using stringent criteria differs from premalignant or malignant oral lesions but is similar to epithelium from benign oral lesions. To further investigate this genetic line of evidence, biopsy specimens diagnosed as fibroma, OLP, low-grade dysplasia, high-grade dysplasia, and SCC were retrieved from the archives of the Oral Pathology Consultants at the Ohio State University. Using laser capture microdissection, tissue of interest was captured from each case and DNA subsequently extracted. Fluorescently labeled PCR primers were used to amplify DNA at 3 tumor suppressor gene loci (3p14.2, 9p21, and 17p13) and evaluated for LOH or microsatellite instability (MSI). OLP was found to be significantly different from low-grade dysplasia, high-grade dysplasia, and SCC when LOH/MSI was found at more than 1 loci (P = .011, P = .032, P = .003), but not different from benign fibromas (P = .395). In agreement with previous studies, well-documented cases of OLP diagnosed using stringent criteria exhibit a genetic profile more similar to a benign or reactive process than a premalignant/malignant one. These findings do not support the classification of OLP as a premalignant condition.
口腔扁平苔藓是一种相对常见的免疫介导的黏膜疾病,好发于中年女性。尽管它被归类为癌前病变,但这种分类仍存在争议。一些作者使用严格的诊断标准发现,口腔扁平苔藓患者患口腔鳞状细胞癌的风险并未增加。可靠但有限的遗传学证据也表明,使用严格标准诊断的口腔扁平苔藓患者的上皮组织与癌前或恶性口腔病变不同,但与良性口腔病变的上皮相似。为了进一步研究这一遗传学证据线索,从俄亥俄州立大学口腔病理咨询中心的档案中检索了诊断为纤维瘤、口腔扁平苔藓、低度发育异常、高度发育异常和鳞状细胞癌的活检标本。使用激光捕获显微切割技术,从每个病例中捕获感兴趣的组织,随后提取DNA。使用荧光标记的PCR引物在3个肿瘤抑制基因位点(3p14.2、9p21和17p13)扩增DNA,并评估杂合性缺失(LOH)或微卫星不稳定性(MSI)。当在超过1个位点发现LOH/MSI时,发现口腔扁平苔藓与低度发育异常、高度发育异常和鳞状细胞癌有显著差异(P = .011、P = .032、P = .003),但与良性纤维瘤无差异(P = .395)。与先前的研究一致,使用严格标准诊断的记录良好的口腔扁平苔藓病例显示出的基因特征更类似于良性或反应性过程,而不是癌前/恶性过程。这些发现不支持将口腔扁平苔藓归类为癌前病变。