Sunlight ultraviolet irradiation and BRAF V600 mutagenesis in human melanoma

被引:36
作者
Besaratinia, Ahmad [1 ]
Pfeifer, Gerd P. [1 ]
机构
[1] City Hope Natl Med Ctr, Div Biol, Beckman Res Inst, Duarte, CA 91010 USA
关键词
cancer; DNA damage; etiology; mutation; solar mutagenesis; BRAF;
D O I
10.1002/humu.20802
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The incidence of melanoma, the most lethal form of skin cancer, continues to increase in the Western world. In addition to genetic alterations in high, and low-susceptibility genes identified for melanoma, somatic mutations in BRAF gene occur frequently in human melanoma and are distinctively linked to sun exposure. Of significance is a single hotspot codon, i.e., BRAF V600, wherein up to 92% of all mutations arise. Recent work in our laboratory has demonstrated that solar ultraviolet (UV) irradiation triggers mutagenesis through induction of various DNA lesions, many of which capable of producing similar types of mutations, as those seen in BRAF V600 variants in human melanoma. In this review article, we have discussed application of "DNA damage,targeted mutagenicity" of solar UV-irradiation for determining the mechanistic involvement of sunlight UV in BRAF V600 mutagenesis in human melanoma. We envision that establishing "DNA-damage derived mutagenesis" in this exceptionally unique target gene may resolve the underlying mechanism(s) of melanoma-genesis, thus helping define preventive and therapeutic measures against this malignant disease.
引用
收藏
页码:983 / 991
页数:9
相关论文
共 71 条
[1]  
*AM AC DERM, 2007, MEL FACT SHEET
[2]   Effects of a guanine-derived formamidopyrimidine lesion on DNA replication - Translesion DNA synthesis, nucleotide insertion, and extension kinetics [J].
Asagoshi, K ;
Terato, H ;
Ohyama, Y ;
Ide, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (17) :14589-14597
[3]   GENETIC-EFFECTS OF THYMINE GLYCOL - SITE-SPECIFIC MUTAGENESIS AND MOLECULAR MODELING STUDIES - (IONIZING-RADIATION OXIDATIVE DAMAGE HYDROXYL RADICALS) [J].
BASU, AK ;
LOECHLER, EL ;
LEADON, SA ;
ESSIGMANN, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (20) :7677-7681
[4]   Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample [J].
Begg, CB ;
Orlow, I ;
Hummer, AJ ;
Armstrong, BK ;
Kricker, A ;
Marrett, LD ;
Millikan, RC ;
Gruber, SB ;
Anton-Culver, H ;
Zanetti, R ;
Gallagher, RP ;
Dwyer, T ;
Rebbeck, TR ;
Mitra, N ;
Busam, K .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (20) :1507-1515
[5]   DNA lesions induced by UV A1 and B radiation in human cells:: Comparative analyses in the overall genome and in the p53 tumor suppressor gene [J].
Besaratinia, A ;
Synold, TW ;
Chen, HH ;
Chang, C ;
Xi, BX ;
Riggs, AD ;
Pfeifer, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (29) :10058-10063
[6]   Similar mutagenicity of photoactivated porphyrins and ultraviolet A radiation mouse embryonic fibroblasts: Involvement of oxidative DNA lesions in mutagenesis [J].
Besaratinia, A ;
Bates, SE ;
Synold, TW ;
Pfeifer, GP .
BIOCHEMISTRY, 2004, 43 (49) :15557-15566
[7]   G-to-T transversions and small tandem base deletions are the hallmark of mutations induced by ultraviolet a radiation in mammalian cells [J].
Besaratinia, A ;
Synold, TW ;
Xi, BX ;
Pfeifer, GP .
BIOCHEMISTRY, 2004, 43 (25) :8169-8177
[8]  
BESARATINIA A, FASEBJ IN PRESS
[9]   Riboflavin activated by ultraviolet A1 irradiation induces oxidative DNA damage-mediated mutations inhibited by vitamin C [J].
Besaratinia, Ahmad ;
Kim, Sang-in ;
Bates, Steven E. ;
Pfeifer, Gerd P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (14) :5953-5958
[10]   Investigating human cancer etiology by DNA lesion footprinting and mutagenicity analysis [J].
Besaratinia, Ahmad ;
Pfeifer, Gerd P. .
CARCINOGENESIS, 2006, 27 (08) :1526-1537