Number of Nevi and early-life ambient UV exposure are associated with BRAF-mutant melanoma

被引:150
作者
Thomas, Nancy E.
Edmiston, Sharon N.
Alexander, Audrey
Millikan, Robert C.
Groben, Pamela A.
Hao, Honglin
Tolbert, Dawn
Berwick, Marianne
Busam, Klaus
Begg, Colin B.
Mattingly, Dianne
Ollila, David W.
Tse, Chiu Kit
Hummer, Amanda
Lee-Taylor, Julia
Conway, Kathleen
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Dermatol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Epidemiol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Surg, Chapel Hill, NC 27599 USA
[4] Univ New Mexico, Dept Med, Div Epidemiol, Albuquerque, NM 87131 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Biostat, New York, NY 10021 USA
[7] Natl Ctr Atmospher Res, Div Atmospher Chem, Boulder, CO 80307 USA
关键词
D O I
10.1158/1055-9965.EPI-06-1038
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Malignant melanomas often contain BRAF or NRAS mutations, but the relationship of these mutations to ambient UV exposure in combination with phenotypic characteristics is unknown. In a population-based case series from North Carolina, 214 first primary invasive melanoma patients in the year 2000 were interviewed regarding their risk factors. Ambient solar UV exposures were estimated using residential histories and a satellite-based model. Cases were grouped on the basis of BRAF and NRAS somatic mutations, determined using single-strand conformation polymorphism analysis and radiolabeled DNA sequencing, and the risk profiles of these groups were compared. Mutually exclusive BRAF-mutant and NRAS-mutant cases occurred at frequencies of 43.0% and 13.6% with mean ages at diagnosis of 47.3 and 62.1 years, respectively. Tumors from patients with > 14 back nevi were more likely to harbor either a BRAF mutation [age-adjusted odds ratio (OR), 3.2; 95% confidence interval (95% CI), 1.4-7.0] or an NRAS mutation (age-adjusted OR, 1.7; 95% CI, 0.6-4.8) compared with patients with 0 to 4 back nevi. However, BRAF-mutant and NRAS-mutant tumors were distinctive in that BRAF-mutant tumors were characteristic of patients with high early-life ambient UV exposure (adjusted OR, 2.6; 95% CI, 1.2-5.3). When ambient UV irradiance was analyzed by decadal age, high exposure at ages 0 to 20 years was associated with BRAF-mutant cases, whereas high exposure at ages 50 and 60 years was characteristic of NRAS-mutant cases. Our results suggest that although nevus Propensity is important for the occurrence of both BRAF and NRAS-mutant melanomas, ambient UV irradiance influences risk differently based on the age of exposure. The association of BRAF mutations with early-life UV exposure provides evidence in support of childhood sun protection for melanoma prevention.
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页码:991 / 997
页数:7
相关论文
共 61 条
[1]   Rapid p53 sequence analysis in primary lung cancer using an oligonucleotide probe array [J].
Ahrendt, SA ;
Halachmi, S ;
Chow, JT ;
Wu, L ;
Halachmi, N ;
Yang, SC ;
Wehage, S ;
Jen, J ;
Sidransky, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (13) :7382-7387
[2]  
[Anonymous], 1987, HUMAN EXPOSURE ULTRA
[3]  
[Anonymous], NATO ASI SERIES
[4]   The epidemiology of UV induced skin cancer [J].
Armstrong, BK ;
Kricker, A .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2001, 63 (1-3) :8-18
[5]  
Begg CB, 1997, CANCER EPIDEM BIOMAR, V6, P99
[6]   CALCULATION OF POLYCHOTOMOUS LOGISTIC-REGRESSION PARAMETERS USING INDIVIDUALIZED REGRESSIONS [J].
BEGG, CB ;
GRAY, R .
BIOMETRIKA, 1984, 71 (01) :11-18
[7]  
BEGG CB, 1994, CANCER EPIDEM BIOMAR, V3, P173
[8]   A design for cancer case-control studies using only incident cases: experience with the GEM study of melanoma [J].
Begg, Colin B. ;
Hummer, Amanda J. ;
Mujumdar, Urvi ;
Armstrong, Bruce K. ;
Kricker, Anne ;
Marrett, Loraine D. ;
Millikan, Robert C. ;
Gruber, Stephen B. ;
Culver, Hoda Anton ;
Zanetti, Roberto ;
Gallagher, Richard P. ;
Dwyer, Terrence ;
Rebbeck, Timothy R. ;
Busam, Klaus ;
From, Lynn ;
Berwick, Marianne .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2006, 35 (03) :756-764
[9]   Oncogenic Ras and its role in tumor cell invasion and metastasis [J].
Campbell, PM ;
Der, CJ .
SEMINARS IN CANCER BIOLOGY, 2004, 14 (02) :105-114
[10]  
CLARK WH, 1969, CANCER RES, V29, P705