Ko Justin M, Velez Nicole F, Tsao Hensin
Department of Dermatology, Harvard Medical School, Boston, MA, USA.
Semin Cutan Med Surg. 2010 Dec;29(4):210-7. doi: 10.1016/j.sder.2010.10.004.
Melanoma is one of the most aggressive and yet poorly understood of human malignancies. Advances in genomics has allowed a more nuanced understanding of the disease, moving beyond the traditional dysplastic nevus-to-melanoma model and identifying multiple divergent oncogenic pathways leading to melanoma. An understanding of the molecular mechanisms driving melanoma has opened the doors for the development of targeted therapeutic approaches. As we enter the era of personalized medicine, it will be critical for clinicians to both appreciate and be able to determine the molecular profile of their patients' melanoma because this profile will guide risk stratification, genetic counseling, and treatment customization. A review of the divergent pathways of melanoma development is presented here, with a particular emphasis on recently identified mutations, and their implications for patient care.
黑色素瘤是人类最具侵袭性且了解甚少的恶性肿瘤之一。基因组学的进展使人们对该疾病有了更细致入微的认识,超越了传统的发育异常痣到黑色素瘤模型,并确定了导致黑色素瘤的多种不同致癌途径。对驱动黑色素瘤的分子机制的理解为靶向治疗方法的开发打开了大门。随着我们进入个性化医疗时代,临床医生了解并能够确定患者黑色素瘤的分子特征至关重要,因为这一特征将指导风险分层、遗传咨询和治疗定制。本文综述了黑色素瘤发展的不同途径,特别强调了最近发现的突变及其对患者护理的影响。