Interaction of CDKN2A and Sun Exposure in the Etiology of Melanoma in the General Population

被引:6
|
作者
Berwick, Marianne [1 ]
Begg, Colin B. [2 ]
Armstrong, Bruce K. [3 ]
Reiner, Anne S. [2 ]
Thomas, Nancy E. [4 ]
Cook, Linda S. [1 ]
Orlow, Irene [2 ]
Kricker, Anne [3 ]
Marrett, Loraine D. [5 ]
Gruber, Stephen B. [6 ]
Anton-Culver, Hoda [7 ]
Millikan, Robert C. [4 ]
Gallagher, Richard P. [8 ]
Dwyer, Terry [9 ]
Rosso, Stefano [10 ]
Kanetsky, Peter A. [11 ]
Lee-Taylor, Julia [12 ]
机构
[1] Univ New Mexico, Dept Internal Med, Ctr Canc, Albuquerque, NM 87131 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[3] Univ Sydney, Queen Elizabeth II Res Inst D02, Sydney, NSW 2006, Australia
[4] Univ N Carolina, Sch Med, Lineberger Canc Res Ctr, Chapel Hill, NC 27599 USA
[5] Canc Care Ontario, Dept Epidemiol, Toronto, ON, Canada
[6] Univ Michigan, Dept Epidemiol, Ann Arbor, MI 48109 USA
[7] Univ Calif Irvine, Dept Epidemiol, Irvine, CA USA
[8] British Columbia Canc Agcy, Dept Epidemiol, Vancouver, BC V5Z 4E6, Canada
[9] Univ Tasmania, Dept Epidemiol, Menzies Ctr, Hobart, Tas, Australia
[10] Ctr Epidemiol & Prevent Oncol Piedmont, Piedmont Canc Registry, Turin, Italy
[11] Univ Penn, Dept Epidemiol, Philadelphia, PA 19104 USA
[12] Natl Ctr Atmospher Res, Div Atmospher Chem, Boulder, CO 80307 USA
关键词
CUTANEOUS MALIGNANT-MELANOMA; RISK-FACTORS; MUTATIONS;
D O I
10.1038/jid.2011.235
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:2500 / 2503
页数:4
相关论文
共 50 条
  • [31] Intronic sequence variants of the CDKN2A gene in melanoma pedigrees
    Harland, M
    Taylor, CF
    Bass, S
    Churchman, M
    Randerson-Moor, JA
    Holland, EA
    Mann, GJ
    Bishop, DT
    Bishop, JAN
    GENES CHROMOSOMES & CANCER, 2005, 43 (02): : 128 - 136
  • [32] CDKN2A mutation analysis in patients with melanoma and breast cancer
    Nagore, E.
    Botella-Estrada, R.
    Garcia-Casado, Z.
    Chirivella, I
    Soriano, V
    Lluch, A.
    Guillen, C.
    ARCHIVES OF DERMATOLOGICAL RESEARCH, 2007, 299 (5-6) : 292 - 292
  • [33] A large intergenic deletion upstream of CDKN2A predisposes melanoma
    Johansson, P. A.
    Nathan, V.
    Howlie, M.
    Symmons, J.
    Hamilton, H.
    Law, M. H.
    Holland, E. A.
    Palmer, J.
    Mann, G. J.
    Hayward, N. K.
    Pritchard, A. L.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1550 - 1551
  • [34] Mutation analysis of the cdkn2a promoter in australian melanoma families
    Pollock P.A.
    Stark M.
    Palmer J.M.
    Walters M.K.
    Martin N.G.
    Green A.C.
    Hayward N.K.
    Nature Genetics, 2001, 27 (Suppl 4) : 80 - 80
  • [35] Genetics of familial melanoma: 20 years after CDKN2A
    Aoude, Lauren G.
    Wadt, Karin A. W.
    Pritchard, Antonia L.
    Hayward, Nicholas K.
    PIGMENT CELL & MELANOMA RESEARCH, 2015, 28 (02) : 148 - 160
  • [36] Mutation analysis of the CDKN2A promoter in Australian melanoma families
    Pollock, PM
    Stark, MS
    Palmer, JM
    Walters, MK
    Aitken, JF
    Martin, NG
    Hayward, NK
    GENES CHROMOSOMES & CANCER, 2001, 32 (01): : 89 - 94
  • [37] Absence of Germline Epimutation of the CDKN2A Gene in Familial Melanoma
    van Doorn, Remco
    Zoutman, Willem H.
    Gruis, Nelleke A.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 (03) : 781 - 784
  • [38] CDKN2A testing and genetic counseling promote reductions in objectively measured sun exposure one year later
    Stump, Tammy K.
    Aspinwall, Lisa G.
    Drummond, Danielle M.
    Taber, Jennifer M.
    Kohlmann, Wendy
    Champine, Marjan
    Cassidy, Pamela B.
    Petrie, Tracy
    Liley, Ben
    Leachman, Sancy A.
    GENETICS IN MEDICINE, 2020, 22 (01) : 26 - 34
  • [39] Analysis of mutations in the p16/CDKN2A gene in sporadic and familial melanoma in the Polish population
    Lamperska, K
    Karczewska, A
    Kwiatkowska, E
    Mackiewicz, A
    ACTA BIOCHIMICA POLONICA, 2002, 49 (02) : 369 - 376
  • [40] Efficacy of novel melanoma treatments in metastatic melanoma patients with germline CDKN2A mutations
    Helgadottir, Hildur
    Ghiorzo, Paola
    van Doorn, Remco
    Puig, Susana
    Levin, Max
    Kefford, Richard
    Queirolo, Paola
    Pastorino, Lorenza
    Lauss, Martin
    Olsson, Hakan
    Hoiom, Veronica
    Jonsson, Goran
    JOURNAL OF TRANSLATIONAL MEDICINE, 2019, 17