Regezi Joseph A, Dekker Nusi P, Ramos Daniel M, Li Xiaowu, Macabeo-Ong Maricris, Jordan Richard C K
Division of Oral Medicine, Pathology and Radiology, School of Dentistry, University of California San Francisco, USA.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002 Dec;94(6):724-31. doi: 10.1067/moe.2002.129760.
Oral warts arising in human immunodeficiency virus (HIV) infection occasionally show marked epithelial dysplasia. However, anecdotal evidence suggests that they do not progress to oral squamous cell carcinoma (SCC). Therefore, we evaluated lesions for expression of proteins (tenascin-C, beta6 integrin, and matrix metalloproteinase-1[MMP1]) that have been identified as important in the invasive phase of oral SCC.
Twenty-two oral dysplastic warts from 22 patients and 5 oral SCCs were stained for human papillomavirus (HPV) antigen, proliferation protein Ki-67, tenascin-C, beta6, and MMP1 by immunohistochemical methods. For comparison, 5 nondysplastic warts each from HIV-positive and HIV-negative patients and 5 normal mucosa specimens were included. Sections were semiquantitatively assessed, and results were compared. Because MMP1 was the lowest or least expressed interface protein, MMP1 mRNA was quantitatively assessed from formalin-fixed paraffin-embedded tissue in selected cases with quantitative reverse transcription-polymerase chain reaction.
Twenty of 22 dysplastic warts stained positive for human papillomavirus common antigen, and all warts showed high proliferative fractions similar to SCCs. Tenascin-C and beta6 were variably expressed by the dysplastic warts but were consistently expressed at high levels in the SCCs. MMP1 protein levels were negative or low in 20 of 22 in dysplastic warts, but were elevated in 4 of 5 SCCs. MMP1 mRNA analysis indicated that message was low in 4 dysplastic warts and also suggested that protein translation was incomplete in 3 of the warts.
We conclude that invasion-associated proteins are underexpressed in oral dysplastic warts in HIV-positive men. However, until these patients are followed for extended periods, the risk of development of SCC from oral dysplastic warts remains unknown.
人类免疫缺陷病毒(HIV)感染引起的口腔疣偶尔会表现出明显的上皮发育异常。然而,有轶事证据表明它们不会进展为口腔鳞状细胞癌(SCC)。因此,我们评估了病变中在口腔SCC侵袭阶段被确定为重要的蛋白质(腱生蛋白-C、β6整合素和基质金属蛋白酶-1[MMP1])的表达情况。
采用免疫组织化学方法,对22例患者的22个口腔发育异常疣和5例口腔SCC进行人乳头瘤病毒(HPV)抗原、增殖蛋白Ki-67、腱生蛋白-C、β6和MMP1染色。作为对照,纳入了HIV阳性和HIV阴性患者各5个非发育异常疣以及5个正常黏膜标本。对切片进行半定量评估,并比较结果。由于MMP1是表达最低或最少的界面蛋白,因此在选定病例中,采用定量逆转录-聚合酶链反应从福尔马林固定石蜡包埋组织中对MMP1 mRNA进行定量评估。
22个发育异常疣中有20个HPV共同抗原染色呈阳性,所有疣均显示出与SCC相似的高增殖分数。腱生蛋白-C和β6在发育异常疣中的表达各不相同,但在SCC中始终高表达。22个发育异常疣中有20个MMP1蛋白水平为阴性或低水平,但5例SCC中有4例MMP1蛋白水平升高。MMP1 mRNA分析表明,4个发育异常疣中的mRNA水平较低,并且还提示其中3个疣的蛋白质翻译不完整。
我们得出结论,HIV阳性男性的口腔发育异常疣中与侵袭相关的蛋白表达不足。然而,在对这些患者进行长期随访之前,口腔发育异常疣发展为SCC的风险仍然未知。