Stephen Josena K, Chen Kang Mei, Shah Veena, Schweitzer Vanessa G, Gardner Glendon, Benninger Michael S, Worsham Maria J
Department of Otolaryngology-Head and Neck Surgery and Research Division, Henry Ford Hospital, Detroit, MI 48202.
Int J Head Neck Surg. 2010 May;1(2):69-77. doi: 10.5005/jp-journals-10001-1013.
This study examined the contribution of promoter hypermethylation to the pathogenesis of respiratory papillomatosis (RP), including recurrences (RRP) and progression to squamous cell carcinoma (SSC). MATERIALS AND METHODS: A retrospective cohort of 25 laryngeal papilloma cases included 21 RRP, two of which progressed to SCC. Aberrant methylation status was determined using the multi-gene (22 tumor suppressor genes) methylation-specific multiplex ligation-dependent probe amplification assay and confirmed using methylation specific PCR. RESULTS: Twenty genes had altered DNA methylation in 22 of 25 cases. Aberrant methylation of CDKN2B and TIMP3 was most frequent. Promoter hypermethylation of BRCA2, APC, CDKN2A and CDKN2B was detected in 2 RRP cases with subsequent progression to SCC. Of the 25 cases, 22 were positive for HPV-6, 2 for HPV-11 and 1 for HPV-16 and 33. CONCLUSIONS: Consistent aberrant methylation of multiple tumor suppressor genes contributes to the pathogenesis of laryngeal papillomas. Persistent aberrant DNA methylation events in 2 RRP cases that progressed to cancer indicate an epigenetic monoclonal progression continuum to SCC.
本研究探讨启动子高甲基化在呼吸道乳头状瘤病(RP)发病机制中的作用,包括复发性呼吸道乳头状瘤病(RRP)以及进展为鳞状细胞癌(SSC)的情况。
对25例喉乳头状瘤病例进行回顾性队列研究,其中包括21例RRP,其中2例进展为SCC。使用多基因(22个肿瘤抑制基因)甲基化特异性多重连接依赖探针扩增法确定异常甲基化状态,并通过甲基化特异性PCR进行确认。
25例中的22例有20个基因发生DNA甲基化改变。CDKN2B和TIMP3的异常甲基化最为常见。在2例随后进展为SCC的RRP病例中检测到BRCA2、APC、CDKN2A和CDKN2B的启动子高甲基化。25例中,22例HPV-6阳性,2例HPV-11阳性,1例HPV-16和33阳性。
多个肿瘤抑制基因持续存在的异常甲基化有助于喉乳头状瘤的发病机制。2例进展为癌症的RRP病例中持续存在的异常DNA甲基化事件表明存在向SCC的表观遗传单克隆进展连续体。