Congenital melanocytic nevi frequently harbor NRAS mutations but no BRAF mutations

被引:230
作者
Bauer, Juergen
Curtin, John A.
Pinkel, Dan
Bastian, Boris C.
机构
[1] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[4] Univ Tubingen, Dept Dermatol, Tubingen, Germany
关键词
D O I
10.1038/sj.jid.5700490
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Most melanocytic nevi develop on sun-exposed skin during childhood and adolescence and commonly harbor BRAF mutations or, less frequently, NRAS mutations. A small subset of nevi is present at birth, and therefore must develop independently of UV light. To assess whether these nevi have a different mutation spectrum than those that develop on sun-exposed skin, we determined the BRAF and NRAS mutation frequencies in 32 truly congenital nevi. We found no BRAF mutations, but 81% (26/32) harbored mutations in NRAS. Consistently, seven of 10 (70%) proliferating nodules that developed early in life in congenital nevi showed mutations in NRAS. A separate set of nevi that displayed histological features frequently found in nevi present at birth ("congenital pattern nevi") but lacked a definitive history of presence at birth showed an inverse mutation pattern with common BRAF mutations (20/28 or 71%) and less frequent NRAS mutations (7/28 or 25%). Thus, nevi that develop in utero are genetically distinct from those that develop later, and histopathologic criteria alone are unable to reliably distinguish the two groups. The results are consistent with the finding in melanoma that BRAF mutations are uncommon in neoplasms that develop in the absence of sun-exposure.
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页码:179 / 182
页数:4
相关论文
共 23 条
[11]   CONGENITAL NEVOCYTIC NEVI AND MALIGNANT MELANOMAS [J].
KOPF, AW ;
BART, RS ;
HENNESSEY, P .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1979, 1 (02) :123-130
[12]   Determinants of BRAF mutations in primary melanomas [J].
Maldonado, JL ;
Fridlyand, J ;
Patel, H ;
Jain, AN ;
Busam, K ;
Kageshita, T ;
Ono, T ;
Albertson, DG ;
Pinkel, D ;
Bastian, BC .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (24) :1878-1880
[13]   CONGENITAL MELANOCYTIC NEVI OF SMALL AND GARMENT TYPE - CLINICAL, HISTOLOGIC, AND ULTRASTRUCTURAL STUDIES [J].
MARK, GJ ;
MIHM, MC ;
LITEPLO, MG ;
REED, RJ ;
CLARK, WH .
HUMAN PATHOLOGY, 1973, 4 (03) :395-418
[14]  
Papp T, 1999, J MED GENET, V36, P610
[15]   High frequency of BRAF mutations in nevi [J].
Pollock, PM ;
Harper, UL ;
Hansen, KS ;
Yudt, LM ;
Stark, M ;
Robbins, CM ;
Moses, TY ;
Hostetter, G ;
Wagner, U ;
Kakareka, J ;
Salem, G ;
Pohida, T ;
Heenan, P ;
Duray, P ;
Kallioniemi, O ;
Hayward, NK ;
Trent, JM ;
Meltzer, PS .
NATURE GENETICS, 2003, 33 (01) :19-20
[16]  
RHODES AR, 1982, J PEDIATR-US, V100, P219, DOI 10.1016/S0022-3476(82)80638-0
[17]   A HISTOLOGIC COMPARISON OF CONGENITAL AND ACQUIRED NEVOMELANOCYTIC NEVI [J].
RHODES, AR ;
SILVERMAN, RA ;
HARRIST, TJ ;
MELSKI, JW .
ARCHIVES OF DERMATOLOGY, 1985, 121 (10) :1266-1273
[18]   THE MALIGNANT POTENTIAL OF SMALL CONGENITAL NEVOCELLULAR NEVI [J].
RHODES, AR ;
SOBER, AJ ;
DAY, CL ;
MELSKI, JW ;
HARRIST, TJ ;
MIHM, MC ;
FITZPATRICK, TB .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1982, 6 (02) :230-241
[19]   BRAF point mutations in primary melanoma show different prevalences by subtype [J].
Sasaki, Y ;
Niu, CB ;
Makino, R ;
Kudo, C ;
Sun, CL ;
Watanabe, H ;
Matsunaga, J ;
Takahashi, K ;
Tagami, H ;
Aiba, S ;
Horii, A .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 123 (01) :177-183
[20]   Congenital melanocytic nevi: Clinical and histopathologic features, risk of melanoma, and clinical management [J].
Tannous, ZS ;
Mihm, MC ;
Sober, AJ ;
Duncan, LM .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2005, 52 (02) :197-203