Identification by cDNA microarray technology of genes modulated by artificial ultraviolet radiation in normal human melanocytes:: Relation to melanocarcinogenesis

被引:37
作者
Valéry, C [1 ]
Grob, JJ [1 ]
Verrando, P [1 ]
机构
[1] Univ Mediterranee, LIMP, F-13009 Marseille, France
关键词
DNA microarray; melanocyte; melanoma; UV stress;
D O I
10.1046/j.0022-202x.2001.01607.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Target genes of ultraviolet stress response in cutaneous melanocytes, potentially associated with solar-induced melanocarcinogenesis, were characterized by cDNA microarray technology. In cultured normal human melanocytes, 198 genes out of approximate to 9000 arrayed were found modulated greater than or equal to 1.9 times following artificial ultraviolet - mainly ultraviolet-B - irradiation (100 mJ per cm(2)). Among them, 159 corresponded to known sequences, the encoded proteins being mostly involved in DNA or RNA binding/synthesis/ modification, or ribosomal proteins. The others were transcription factors, receptors, tumor suppressors, and (proto)oncogenes. Members of these families have already been linked to melanoma. In addition, some of the modulated genes were borne by chromosomes harboring candidate melanoma loci. Comparisons with genes modified in melanoma samples reported in previous studies with similar microarray platform showed that 59% of the known genes sensitive to ultraviolet were modulated in the same way. Furthermore, 39 expressed sequence tags were modulated, and preliminary experiments showed that two expressed sequence tags displayed differential expressions both in melanoma cell lines and in melanoma tumors. These results provide a basis for further studies on the role of modulated genes in ultraviolet-induced melanoma. Because some of these genes are potential markers of the disease, they might help for developing new molecular-based strategies for risk prediction in patients.
引用
收藏
页码:1471 / 1482
页数:12
相关论文
共 75 条
[1]   ANALYSIS OF THE UV-INDUCED MELANOGENESIS AND GROWTH ARREST OF HUMAN MELANOCYTES [J].
ABDELMALEK, Z ;
SWOPE, V ;
SMALARA, D ;
BABCOCK, G ;
DAWES, S .
PIGMENT CELL RESEARCH, 1994, 7 (05) :326-332
[2]   UVB-specific regulation of gene expression in human melanocytic cells: cell cycle effects and implication in the generation of melanoma [J].
Ablett, E ;
Pedley, J ;
Dannoy, PA ;
Sturm, RA ;
Parsons, PG .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1998, 422 (01) :31-41
[3]   Differential stimulation of ERK and JNK activities by ultraviolet B irradiation and epidermal growth factor in human keratinocytes [J].
Assefa, Z ;
Garmyn, M ;
Bouillon, R ;
Merlevede, W ;
Vandenheede, JR ;
Agostinis, P .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1997, 108 (06) :886-891
[4]  
BALE SJ, 1991, NEW ENGL J MED, V324, P925
[5]   Gene regulation in melanoma progression by the AP-2 transcription factor [J].
Bar-Eli, M .
PIGMENT CELL RESEARCH, 2001, 14 (02) :78-85
[6]  
BARKER D, 1995, CANCER RES, V55, P4041
[7]   Gene expression informatics - it's all in your mine [J].
Bassett, DE ;
Eisen, MB ;
Boguski, MS .
NATURE GENETICS, 1999, 21 (Suppl 1) :51-55
[8]   Detection of differentially regulated genes in keratinocytes by cDNA array hybridization: Hsp27 and other novel players in response to artificial ultraviolet radiation [J].
Becker, B ;
Vogt, T ;
Landthaler, M ;
Stolz, W .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 116 (06) :983-988
[9]  
Benoliel AM, 1997, J CELL SCI, V110, P2089
[10]   Successive alteration and recovery of epidermal differentiation and morphogenesis after specific UVB-damages in skin reconstructed in vitro [J].
Bernerd, F ;
Asselineau, D .
DEVELOPMENTAL BIOLOGY, 1997, 183 (02) :123-138