《口腔颌面外科杂志》

• 基础研究 • 上一篇    下一篇

SOX10作为原发性口腔黏膜恶性黑色素瘤分子诊断指标的初步研究

马旭辉,王丽珍,任国欣,吴云腾,顾挺,郭伟   

  1. 国家口腔疾病临床研究中心,上海市口腔医学重点实验室,上海市口腔医学研究所,上海交通大学医学院附属第九人民医院·口腔医学院 口腔颌面-头颈肿瘤科,上海   200011
  • 出版日期:2019-06-28 发布日期:2019-11-13
  • 通讯作者: 郭 伟,教授. E-mail: guoweicn@sohu.com E-mail:guoweicn@sohu.com
  • 作者简介:马旭辉(1987—),女,甘肃兰州人,住院医师,博士.
  • 基金资助:
    国家重点研发计划项目(2016YFC0905003、2016YFC 0905000;上海交通大学交叉医学(理)基金(ZH2018 QNA09)

A Preliminary Study on SOX10 as A Molecular Diagnostic Marker for Primary Oral Mucosal Melanoma

MA Xu hui, WANG Li zheng, REN Guo xin, WU Yun teng, GU Ting, GUO Wei   

  1. Department of Oromaxillofacial Head and Neck Oncology, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiaotong University School of Medicine; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology; Shanghai Research Institute of Stomatology, Shanghai 200011, China
  • Online:2019-06-28 Published:2019-11-13

摘要: 目的:阐明SOX10在口腔黏膜恶性黑色素瘤的表达特点。方法:通过免疫组织化学染色对89例口腔黏膜恶性黑色素瘤(OMM)及4例口腔黏膜促结缔组织增生型黑色素瘤(ODM) 的石蜡标本中,S-100、HMB-45、Melan-A以及SOX10的表达特点进行分析。结果:在OMM中Melan-A、HMB-45、S-100以及SOX10的表达水平分别为96.6%、93.3%、97.8%及98.8%。在OMM中SOX10的表达水平与S-100、Melan-A无明显统计学差异(P>0.05),但显著高于HMB-45(P<0.05)。在4例ODM中,SOX10与S-100均表达,Melan-A及HMB-45表达均阴性。在OMM及ODM中,SOX10的染色模式均呈强且特异的核染。结论:SOX10可在S-100、Melan-A,HMB-45等常规免疫组化标记物的基础上,作为OMM及ODM病理诊断的有力补充,具有重要的临床应用价值。

关键词:  SOX10;  , 口腔黏膜恶性黑色素瘤;  , 分子诊断;组织病理学;  , 免疫组织化学

Abstract: Objective: To elucidate the expression of SOX10 in primary oral mucosal melanoma (OMM). Methods: The expression of S-100, HMB-45, Melan-A and SOX10 in 89 OMM and 4 ODM(oral mucosal desmoplastic melanoma) in paraffin specimens were analyzed by immunohistochemical staining. Results: In OMM, the expression levels of Melan-A,HMB-45, S-100 and SOX10 were 96.6%, 93.3%, 97.8% and 98.8%, respectively. The expression level of SOX10 in OMM was not significantly different from S-100 and Melan-A (P>0.05), but significantly higher than that of HMB-45 (P<0.05). In 4 ODM cases, SOX10 and S-100 were expressed, while Melan-A and HMB-45 were negative. In OMM and ODM, the staining pattern of SOX10 was strong and specific was present in nuclear. Conclusions: SOX10 could be used as a helpful marker for pathological diagnosis of OMM and ODM on the basis of routine immunohistochemical markers, such as S-100, Melan-A and HMB-45, and is of significant clinical importance.

Key words:  SOX10, primary oral mucosal melanoma (OMM), molecular diagnosis, histopathology, immunohistochemistry

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