Zhang Ling Yan, Smith Matthew L, Schultheis Beate, Fitzgibbon Jude, Lister T Andrew, Melo Junia V, Cross Nicholas C P, Cavenagh Jamie D
Wessex Regional Genetics Laboratory, Salisbury, UK.
Leuk Res. 2006 Apr;30(4):373-8. doi: 10.1016/j.leukres.2005.08.015. Epub 2005 Sep 22.
KIT mutation has been implicated in sporadic mastocytosis, yet clusters in only a few sites in the molecule. For those malignancies associated with KIT mutation or over-expression, imatinib offers a specific therapeutic option, yet it has no effect on D816V mutation commonly seen in sporadic mastocytosis. The majority of cases of familial mastocytosis seem to lack KIT mutation. We report a kindred with mastocytosis in whom in vitro and in vivo sensitivity to imatinib was demonstrated. Mutation analysis of the KIT coding region in this family identified a novel A>T mutation at nucleotide 1547 [K509I] in exon 9 in both of the affected patients.
KIT突变与散发性肥大细胞增多症有关,但仅聚集在分子的少数位点。对于那些与KIT突变或过表达相关的恶性肿瘤,伊马替尼提供了一种特异性治疗选择,但它对散发性肥大细胞增多症中常见的D816V突变无效。大多数家族性肥大细胞增多症病例似乎缺乏KIT突变。我们报告了一个肥大细胞增多症家族,该家族成员对伊马替尼表现出体内外敏感性。对这个家族中KIT编码区的突变分析在两名受影响患者的第9外显子中鉴定出一个新的核苷酸1547处的A>T突变[K509I]。