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A brief history of melanoma: From mummies to mutations

机译:黑色素瘤的简要历史:从木乃伊到突变

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In recent years, melanoma research has undergone a renaissance. What was once viewed, at least in the metastatic setting, as an intractable and untreatable disease is now revealing its molecular weaknesses. 2011 was a landmark year for melanoma therapy, with two new agents, the anti-CTLA4 antibody ipilimumab and the BRAF inhibitor vemurafenib, shown to confer a survival benefit in randomized phase III clinical trials. Overlooked in the recent flurry of interest that has accompanied the development of these drugs, melanoma is in fact an ancient disease that has long frustrated attempts at therapeutic interventions. In this article, we trace the history of melanoma: from the earliest known cases of melanoma in pre-Colombian South America, through the explorations of the Victorian anatomists right up to the molecular biology revolution of the 20th century that allowed for the identification of the key driving events required for melanomagenesis. We further outline how observations about melanoma heterogeneity, first made over 190 years ago, continue to drive our efforts to reduce melanoma to the level of a chronic, manageable disease and ultimately to cure it entirely. Melanoma Res 22:114-122
机译:近年来,黑色素瘤的研究已经复兴。曾经至少在转移性环境中被视为难治且无法治愈的疾病,现在正在揭示其分子弱点。 2011年是黑色素瘤治疗具有里程碑意义的一年,抗CTLA4抗体ipilimumab和BRAF抑制剂vemurafenib两种新药在随机III期临床试验中显示出生存优势。在伴随着这些药物的发展而引起的近期关注中,黑素瘤实际上被忽视了,实际上它是一种古老的疾病,长期以来一直在挫败治疗性干预的尝试。在本文中,我们追溯了黑色素瘤的历史:从南美前哥伦布时期最早的黑色素瘤病例,到维多利亚时代的解剖学家的探索,直到20世纪的分子生物学革命,才得以鉴定出黑色素瘤。黑色素生成所需的关键驾驶事件。我们进一步概述了关于黑素瘤异质性的观察结果(始于190年前)如何继续推动我们努力将黑素瘤减少至慢性,可控制的疾病水平,并最终将其完全治愈。黑色素瘤研究22:114-122

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