The interdependence of skin aging, skin cancer, and DNA repair capacity: A novel perspective with therapeutic implications

被引:24
作者
Goukassian, DA [1 ]
Gilchrest, BA [1 ]
机构
[1] Boston Univ, Sch Med, Dept Dermatol, Boston, MA 02118 USA
关键词
D O I
10.1089/rej.2004.7.175
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The human body is constantly exposed to exogenous and endogenous insults that threaten its genomic integrity and that lead to changes at the molecular, biochemical, and cellular levels. As a major interface between the environment and the internal milieu, our skin is especially subject to such events. Common insults include but are not limited to infectious agents, environmental pollutions and toxins, carcinogens, and ultraviolet (UV) irradiation. It is estimated that there are thousands of DNA alterations in each cell daily.(1) Therefore, if not efficiently repaired, our genome would rapidly be destroyed. This review focuses predominantly on UV-induced DNA damage in human skin, protective molecular responses to UV damage, and the consequences of these opposing forces for aging and photocarcinogenesis.
引用
收藏
页码:175 / 185
页数:11
相关论文
共 99 条
  • [1] *AM CANC SOC, 2000, CANC FACTS FIG 2000
  • [2] Berg RJW, 2000, CANCER RES, V60, P2858
  • [3] PLASMID-BASED TRANSGENIC MOUSE MODEL FOR STUDYING IN-VIVO MUTATIONS
    BOERRIGTER, METI
    DOLLE, MET
    MARTUS, HJ
    GOSSEN, JA
    VIJG, J
    [J]. NATURE, 1995, 377 (6550) : 657 - 659
  • [4] Ultraviolet irradiation induces multiple DNA double-strand breaks and apoptosis in normal granulocytes and chronic myeloid leukaemia blasts
    Bogdanov, KV
    Chukhlovin, AB
    Zaritskey, AY
    Frolova, OI
    Afanasiev, BV
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1997, 98 (04) : 869 - 872
  • [5] DNA-DAMAGE, MUTATION AND FINE-STRUCTURE DNA-REPAIR IN AGING
    BOHR, VA
    ANSON, RM
    [J]. MUTATION RESEARCH-DNAGING GENETIC INSTABILITY AND AGING, 1995, 338 (1-6): : 25 - 34
  • [6] THE CELLULAR-RESPONSES TO DNA-DAMAGE
    CARR, AM
    HOEKSTRA, MF
    [J]. TRENDS IN CELL BIOLOGY, 1995, 5 (01) : 32 - 40
  • [7] MUTATION AND EXPRESSION OF THE XPA GENE IN REVERTANTS AND HYBRIDS OF A XERODERMA-PIGMENTOSUM CELL-LINE
    CLEAVER, JE
    MCDOWELL, M
    JONES, C
    WOOD, R
    KARENTZ, D
    [J]. SOMATIC CELL AND MOLECULAR GENETICS, 1994, 20 (04) : 327 - 337
  • [8] Thymidine dinucleotides inhibit contact hypersensitivity and activate the gene for tumor necrosis factor α
    Cruz, PD
    Leverkus, M
    Dougherty, I
    Gleason, MJ
    Eller, M
    Yaar, M
    Gilchrest, BA
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (02) : 253 - 258
  • [9] Inhibition of the elicitation phase of contact hypersensitivity by thymidine dinucleotides is in part mediated by increased expression of interleukin-10 in human keratinocytes
    Curiel-Lewandrowski, C
    Venna, SS
    Eller, MS
    Cruikshank, W
    Dougherty, I
    Cruz, PD
    Gilchrest, BA
    [J]. EXPERIMENTAL DERMATOLOGY, 2003, 12 (02) : 145 - 152
  • [10] Induction of DNA adducts and mutations in spleen, liver and lung of XPA-deficient/lacZ transgenic mice after oral treatment with benzo[a]pyrene:: correlation with tumour development
    de Vries, A
    Dollé, MET
    Broekhof, JLM
    Muller, JJA
    Kroese, ED
    van Kreijl, CF
    Capel, PJA
    Vijg, J
    van Steeg, H
    [J]. CARCINOGENESIS, 1997, 18 (12) : 2327 - 2332