A brief history of melanoma: from mummies to mutations

被引:99
作者
Rebecca, Vito W. [1 ,2 ]
Sondak, Vernon K. [2 ,3 ]
Smalley, Keiran S. M. [1 ,2 ,3 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Mol Oncol, Tampa, FL 33612 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Comprehens Melanoma Res Ctr, Tampa, FL 33612 USA
[3] H Lee Moffitt Canc Ctr & Res Inst, Dept Cutaneous Oncol, Tampa, FL 33612 USA
关键词
BRAF; melanoma; oncogenes; surgery; BRAF MUTATIONS; INHIBITOR RESISTANCE; TRANSFORMING GENE; SOMATIC MUTATIONS; UVEAL MELANOMA; MITOTIC RATE; RED HAIR; B-RAF; CANCER; ONCOGENE;
D O I
10.1097/CMR.0b013e328351fa4d
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:114 / 122
页数:9
相关论文
共 98 条
[41]   Coexisting NRAS and BRAF Mutations in Primary Familial Melanomas with Specific CDKN2A Germline Alterations [J].
Jovanovic, Braslav ;
Egyhazi, Suzanne ;
Eskandarpour, Malihe ;
Ghiorzo, Paola ;
Palmer, Jane M. ;
Scarra, Giovanna Bianchi ;
Hayward, Nicholas K. ;
Hansson, Johan .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2010, 130 (02) :618-620
[42]   Hyperactivation of MEK-ERK1/2 signaling and resistance to apoptosis induced by the oncogenic B-RAF inhibitor, PLX4720, in mutant N-RAS melanoma cells [J].
Kaplan, F. M. ;
Shao, Y. ;
Mayberry, M. M. ;
Aplin, A. E. .
ONCOGENE, 2011, 30 (03) :366-371
[43]   Rnd3 Regulation of the Actin Cytoskeleton Promotes Melanoma Migration and Invasive Outgrowth in Three Dimensions [J].
Klein, R. Matthew ;
Aplin, Andrew E. .
CANCER RESEARCH, 2009, 69 (06) :2224-2233
[44]   Meta-analysis of phase II cooperative group trials in metastatic stage IV melanoma to determine progression-free and overall survival benchmarks for future phase II trials [J].
Korn, Edward L. ;
Liu, Ping-Yu ;
Lee, Sandra J. ;
Chapman, Judith-Anne W. ;
Niedzwiecki, Donna ;
Suman, Vera J. ;
Moon, James ;
Sondak, Vernon K. ;
Atkins, Michael B. ;
Eisenhauer, Elizabeth A. ;
Parulekar, Wendy ;
Markovic, Svetomir N. ;
Saxman, Scott ;
Kirkwood, John M. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (04) :527-534
[45]   DYSPLASTIC NEVI AS PRECURSORS TO HEREDITARY MELANOMA [J].
KRAEMER, K .
JOURNAL OF DERMATOLOGIC SURGERY AND ONCOLOGY, 1983, 9 (08) :619-622
[46]  
Laennec R.T.H., 1812, B LECOLE SOCIETIE ME, V1, P24
[47]  
LANCASTER H O, 1956, Med J Aust, V43, P1082
[48]  
LANCASTER H. O., 1957, MED JOUR AUSTRALIA, VI 44, P452
[49]   Polyclonality of BRAF mutations in primary melanoma and the selection of mutant alleles during progression [J].
Lin, J. ;
Goto, Y. ;
Murata, H. ;
Sakaizawa, K. ;
Uchiyama, A. ;
Saida, T. ;
Takata, M. .
BRITISH JOURNAL OF CANCER, 2011, 104 (03) :464-468
[50]   Prognostic and Clinicopathologic Associations of Oncogenic BRAF in Metastatic Melanoma [J].
Long, Georgina V. ;
Menzies, Alexander M. ;
Nagrial, Adnan M. ;
Haydu, Lauren E. ;
Hamilton, Anne L. ;
Mann, Graham J. ;
Hughes, T. Michael ;
Thompson, John F. ;
Scolyer, Richard A. ;
Kefford, Richard F. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (10) :1239-1246