国际肿瘤学杂志 ›› 2018, Vol. 45 ›› Issue (1): 59-.doi: 10.3760/cma.j.issn.1673-422X.2018.01.014

• 综述 • 上一篇    下一篇

黑色素瘤的生物标志物

王燕军,康晓静   

  1. 830001 乌鲁木齐,新疆医科大学研究生学院;新疆维吾尔自治区人民医院皮肤性病科
  • 出版日期:2018-01-08 发布日期:2018-02-12
  • 通讯作者: 康晓静 E-mail:drkangxj666@163.com
  • 基金资助:
    新疆维吾尔自治区自然科学基金(2016D01C101)

Biomarkers for malignant melanoma

Wang Yanjun, Kang Xiaojing   

  1. Postgraduate School of Xinjiang Medical University; Department of Dermatology and Venereology, People′s Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830001, China
  • Online:2018-01-08 Published:2018-02-12
  • Contact: Kang Xiaojing E-mail:drkangxj666@163.com
  • Supported by:
    Natural Science Foundation of Xinjiang Uygur Autonomous Region of China (2016D01C101)

摘要: 黑色素瘤是一种侵袭性强的恶性肿瘤,其发病机制尚不清楚,这可能限制了黑色素瘤的研究及其生物标志物和治疗的发展。近年来,随着对黑色素瘤发病机制的深入研究和分子生物学技术的发展,发现一些新型生物标志物在黑色素瘤中发挥着重要作用。遗传和表观遗传因素是黑色素瘤发生和发展的重要原因,其中遗传基因突变是黑色素瘤重要的生物标志物,可为患者提供预后和个体化治疗的重要信息。表观遗传改变可作为诊断黑色素瘤的一种非侵入性手段,也可作为判断预后和预测疾病的新型生物标志物。黑色素瘤生物标志物的发现为疾病早期诊断、个体化治疗和判断预后提供了理论基础。

关键词: 黑色素瘤; 遗传学; 后成说, 遗传; 生物学标记

Abstract: Malignant melanoma is one of the most aggressive cancers. The pathogenesis of melanoma has not been well documented, which may restrict the research and development of biomarkers and therapies. Recently, with the further study of the pathogenesis of melanoma and the development of molecular biology techniques, some new biomarkers have been found to play an important role in melanoma. Several genetic and epigenetic factors have been identified as contributing to the development and progression of melanoma. Considerable efforts have been made to classify melanoma into distinct subtypes based on genetic mutations and gene expression profile offer important information on patients′ prognosis and individual treatment options. Epigenetic alterations can be used as a noninvasive diagnostic tool for melanoma and can be used as a new biomarker for predicting prognosis and predicting disease. And the discovery of biomarkers for melanoma provides a theoretical basis for early diagnosis, individualized treatment and prognosis.

Key words: Melanoma, Genetics, Epigenesis, genetic, Biomarkers