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口腔扁平苔藓的分子分析。一种癌前病变?

Molecular analysis of oral lichen planus. A premalignant lesion?

作者信息

Zhang L, Michelsen C, Cheng X, Zeng T, Priddy R, Rosin M P

机构信息

Faculty of Dentistry, University of British Columbia, Vancouver, Canada.

出版信息

Am J Pathol. 1997 Aug;151(2):323-7.

PMID:9250145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1858013/
Abstract

Oral lichen planus (OLP) is a common mucosal condition that is considered premalignant by some, although others argue that only lichenoid lesions with dysplasia are precancerous. To address the question of whether OLP without dysplasia is premalignant, we used microsatellite analysis to examine 33 cases of OLP for allelic loss at nine loci located on chromosomes 3p, 9p, and 17p. Loss of heterozygosity (LOH) on these three arms occurs frequently in oral tumors, and the presence of these alterations in premalignant lesions suggests that they may play an important role in tumor progression. Results were compared with those observed in oral dysplasias (10 mild, 11 moderate, 16 severe/carcinoma in situ), 22 oral squamous cell carcinomas, and 29 reactive lesions. LOH was present in 6% of OLP, 14% of reactive lesions, 40% of mild dysplasia, 46% of moderate dysplasia, 81% of severe dysplasia/carcinoma in situ, and 91% of squamous cell carcinomas. LOH was detected on only a single arm in OLP and reactive lesions but occurred on more than one chromosome in dysplasia and cancer, and the frequency of this multiple loss correlated significantly with increasing degrees of dysplasia and progression into squamous cell carcinoma (P = 0.0028). Although these findings do not support OLP as a lesion at risk for malignant transformation, such results need to be confirmed by use of other genetic markers as OLP may undergo malignant transformation through genetic pathways different from those of oral dysplasia.

摘要

口腔扁平苔藓(OLP)是一种常见的黏膜疾病,一些人认为它具有恶变倾向,尽管也有人认为只有伴有发育异常的苔藓样病变才具有癌前病变性质。为了探讨无发育异常的OLP是否具有恶变倾向,我们采用微卫星分析方法,检测了33例OLP患者位于3号、9号和17号染色体上9个位点的等位基因缺失情况。这三条染色体臂上的杂合性缺失(LOH)在口腔肿瘤中经常出现,而这些改变在癌前病变中的存在表明它们可能在肿瘤进展中起重要作用。将结果与口腔发育异常(10例轻度、11例中度、16例重度/原位癌)、22例口腔鳞状细胞癌和29例反应性病变的检测结果进行比较。LOH在6%的OLP、14%的反应性病变、40%的轻度发育异常、46%的中度发育异常、81%的重度发育异常/原位癌以及91%的鳞状细胞癌中出现。在OLP和反应性病变中,LOH仅在一条染色体臂上被检测到,但在发育异常和癌症中,LOH发生在多条染色体上,这种多重缺失的频率与发育异常程度的增加以及向鳞状细胞癌的进展显著相关(P = 0.0028)。尽管这些发现不支持OLP是具有恶变风险的病变,但由于OLP可能通过与口腔发育异常不同的遗传途径发生恶变,因此需要使用其他遗传标记来证实这些结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dd0/1858013/93c65e4a3628/amjpathol00020-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dd0/1858013/93c65e4a3628/amjpathol00020-0017-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dd0/1858013/93c65e4a3628/amjpathol00020-0017-a.jpg

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