Department of Oral and Maxillofacial-Head and Neck Oncology, Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, PR China.
Department of Stomatology, First Affiliated Hospital of Zhejiang University, Hangzhou, PR China.
J Pathol. 2018 Mar;244(3):358-366. doi: 10.1002/path.5017. Epub 2018 Feb 5.
Oral mucosal melanoma (OMM) is a rare and aggressive subtype of melanoma with little known about its pathogenesis or carcinogenesis. We therefore performed whole-exome sequencing (WES) on 19 matched OMM tumor/normal pairs in order to gain insight into potential genetic drivers of tumor formation. For the first time, we describe the comprehensive mutational profile of OMM. Our data suggest that the genetic background of OMM differs from those of other melanoma subtypes. We identified recurrent mutations involving KIT, POLE, PTPRD, PTCHD2, and DMXL2. Notably, copy number analysis revealed recurrently amplified regions of 12q14 (57.9%, containing CDK4) and 5p15 (47.4%, containing TERT). CNV analysis in a separate cohort of 15 samples validated the frequent CNV in CDK4 and TERT. We also observed that the melanocyte development and pigmentation signaling pathway is frequently altered in OMM. Furthermore, our data suggest several altered genes that may be amenable for targeted therapy. We identified one patient with metastatic OMM in our cohort who was identified to harbor a targetable KIT mutation using our WES results. This patient was able to achieve complete remission following implementation of KIT-targeted therapy. These findings provide further insight into the genetic underpinnings of OMM development and suggest that patients with OMM may benefit from WES analysis to identify potential targetable genetic mutations. Copyright © 2017 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
口腔黏膜黑色素瘤(OMM)是一种罕见且侵袭性的黑色素瘤亚型,其发病机制或致癌机制知之甚少。因此,我们对 19 对匹配的 OMM 肿瘤/正常对进行了全外显子组测序(WES),以便深入了解肿瘤形成的潜在遗传驱动因素。我们首次描述了 OMM 的全面突变谱。我们的数据表明,OMM 的遗传背景与其他黑色素瘤亚型不同。我们确定了涉及 KIT、POLE、PTPRD、PTCHD2 和 DMXL2 的复发性突变。值得注意的是,拷贝数分析显示 12q14 (57.9%,包含 CDK4)和 5p15 (47.4%,包含 TERT)的频繁扩增区域。在另一组 15 个样本的 CNV 分析中验证了 CDK4 和 TERT 的频繁 CNV。我们还观察到 OMM 中黑素细胞发育和色素沉着信号通路经常发生改变。此外,我们的数据表明,几个改变的基因可能适合靶向治疗。我们在我们的队列中发现了一名患有转移性 OMM 的患者,该患者的 WES 结果显示存在可靶向的 KIT 突变。该患者在实施 KIT 靶向治疗后实现了完全缓解。这些发现进一步深入了解了 OMM 发展的遗传基础,并表明 OMM 患者可能受益于 WES 分析以确定潜在的可靶向遗传突变。版权所有©2017 英国和爱尔兰病理学会。由 John Wiley & Sons,Ltd 出版。