The genetics of malignant melanoma

被引:21
作者
Lomas, Jesus [1 ]
Martin-Duque, Pilar [2 ]
Pons, Mar [1 ]
Quintanilla, Miguel [1 ]
机构
[1] Univ Autonoma Madrid, CSIC, Inst Invest Biomed Alberto Sols, Madrid 28029, Spain
[2] Univ Francisco Vitoria PM D, Fac Ciencias Biosanitaria, Madrid, Spain
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
melanoma; susceptibility genes; activated signaling pathways; mouse models; wide genomic analyses; gene expression profiles; stem cells; review;
D O I
10.2741/3065
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Melanoma probably is the most aggressive cancer in humans and remains one of the leading causes of cancer death in developed countries. This review summarizes the most important alterations in protooncogenes and tumor suppressor genes that contribute to the pathogenesis of malignant melanoma, with a special emphasis on the involved signaling pathways. Our knowledge of the molecular biology of melanoma has been benefited from recent advances on high-throughput technologies analyzing wide genomic and gene expression profiles that have uncovered unknown candidate genes. To test the interactions between distinct pathways and of those with the environment a wealth of genetically modified animal models has been generated over the past years. Other studies have focused on the isolation of melanoma stem cells and on the characterization of signaling pathways that contribute to their survival and maintenance. A consequence of all these studies is the emergence of potential new strategies that could improve the still unadequate arsenal of therapeutic tools to fight against this fatal disease.
引用
收藏
页码:5071 / 5093
页数:23
相关论文
共 202 条
[1]   MALIGNANT-MELANOMA - A UNIFYING CONCEPT [J].
ACKERMAN, AB .
HUMAN PATHOLOGY, 1980, 11 (06) :591-595
[2]   Metastasizing melanoma formation caused by expression of activated N-RasQ61K on an INK4a-deficient background [J].
Ackermann, J ;
Frutschi, M ;
Kaloulis, K ;
McKee, T ;
Trumpp, A ;
Beermann, F .
CANCER RESEARCH, 2005, 65 (10) :4005-4011
[3]   A high-throughput study in melanoma identifies epithelial-mesenchymal transition as a major determinant of metastasis [J].
Alonso, Soledad R. ;
Tracey, Lorraine ;
Ortiz, Pablo ;
Perez-Gomez, Beatriz ;
Palacios, Jose ;
Pollan, Marina ;
Linares, Juan ;
Serrano, Salvio ;
Saez-Castillo, Ana I. ;
Sanchez, Lydia ;
Pajares, Raquel ;
Sanchez-Aguilera, Abel ;
Artiga, Maria J. ;
Piris, Miguel A. ;
Rodriguez-Peralto, Jose L. .
CANCER RESEARCH, 2007, 67 (07) :3450-3460
[4]   Differential expression of N-cadherin distinguishes a subset of metastasizing desmoplastic melanomas [J].
Attis, Maria Gallego ;
Burchette, James L. ;
Selim, M. Angelica ;
Pham, Tram ;
Soler, Alejandro Peratta .
HUMAN PATHOLOGY, 2006, 37 (07) :899-905
[5]   Chromosomal imbalances in primary and metastatic melanomas revealed by comparative genomic hybridization [J].
Balázs, M ;
Adám, Z ;
Treszl, A ;
Bégány, A ;
Hunyadi, J ;
Adány, R .
CYTOMETRY, 2001, 46 (04) :222-232
[6]   CDNA array technology in melanoma: An overview [J].
Baldi, A ;
Santini, D ;
De Luca, A ;
Paggi, MG .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 196 (02) :219-223
[7]   Activation of Notch1 signaling is required for β-catenin-mediated human primary melanoma progression [J].
Balint, K ;
Xiao, M ;
Pinnix, CC ;
Soma, A ;
Veres, I ;
Juhasz, I ;
Brown, EJ ;
Capobianco, AJ ;
Herlyn, M ;
Liu, ZJ .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (11) :3166-3176
[8]   Dual inactivation of RB and p53 pathways in RAS-induced melanomas [J].
Bardeesy, N ;
Bastian, BC ;
Hezel, A ;
Pinkel, D ;
DePinho, RA ;
Chin, L .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (06) :2144-2153
[9]   Animal models of melanoma: Recent advances and future prospects [J].
Bardeesy, N ;
Wong, KK ;
DePinho, RA ;
Chin, L .
ADVANCES IN CANCER RESEARCH, VOL 79, 2000, 79 :123-156
[10]   Molecular cytogenetic analysis of Spitz nevi shows clear differences to melanoma [J].
Bastian, BC ;
Wesselmann, U ;
Pinkel, D ;
LeBoit, PE .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 113 (06) :1065-1069