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Analysis of V600E BRAF and D816V KIT mutations in systemic mastocytosis
被引:6
|作者:
Hagglund, H.
[1
,2
,3
]
Sander, B.
[2
,4
]
Ahmadi, A.
[4
]
Gulen, T.
[2
,5
,6
]
Nilsson, G.
[2
,6
]
机构:
[1] Karolinska Univ Hosp Huddinge, Dept Hematol, Stockholm, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Mastocytosis Ctr Karolinska, S-17176 Stockholm, Sweden
[3] Uppsala Univ, Univ Uppsala Hosp, Dept Med Sci, Div Hematol, Uppsala, Sweden
[4] Karolinska Univ Hosp Huddinge, Dept Pathol, Stockholm, Sweden
[5] Karolinska Univ Hosp Huddinge, Dept Resp Med & Allergy, Stockholm, Sweden
[6] Karolinska Univ Hosp, Karolinska Inst, Dept Med, Clin Immunol & Allergy Unit, S-17176 Stockholm, Sweden
基金:
瑞典研究理事会;
关键词:
Mastocytosis;
Mast cell;
BRAF;
Mutation;
RENAL-CELL CARCINOMA;
DOSE-RESPONSE METAANALYSIS;
COLORECTAL-CANCER RISK;
DIETARY FIBER;
PROSTATE-CANCER;
PHYSICAL-ACTIVITY;
COHORT;
PATTERNS;
EPIDEMIOLOGY;
DISEASE;
D O I:
10.1007/s12032-014-0123-4
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Most patients with systemic mastocytosis (SM) carry a D816 V KIT mutation causing a ligand-independent activation of the receptor. Down-stream of KIT is several components known to be mutated in different malignancies. RAF is among the most frequently mutated kinases, where BRAF V600E mutation occurs in most hairy cell leukemias (HCL) and half of malignant melanomas. We investigated BRAF mutations in 36 subjects with different forms of SM, but could not detect BRAF mutation in any of the cases, not even in the mast cell lineage of a patient with V600E BRAF-positive HCL. Thus, although BRAF is commonly mutated it appears not to be present in SM.
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页数:13
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