Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/87829
Type: Artigo de periódico
Title: Familial Systemic Mastocytosis With Germline Kit K509i Mutation Is Sensitive To Treatment With Imatinib, Dasatinib And Pkc412
Author: de Melo Campos P.
Machado-Neto J.A.
Scopim-Ribeiro R.
Visconte V.
Tabarroki A.
Duarte A.S.S.
Barra F.F.C.
Vassalo J.
Rogers H.J.
Lorand-Metze I.
Tiu R.V.
Costa F.F.
Olalla Saad S.T.
Traina F.
Abstract: Mastocytosis are myeloproliferative neoplasms commonly related to gain-of-function mutations involving the tyrosine kinase domain of KIT. We herein report a case of familial systemic mastocytosis with the rare KIT K509I germ line mutation affecting two family members: mother and daughter. In vitro treatment with imatinib, dasatinib and PKC412 reduced cell viability of primary mast cells harboring KIT K509I mutation. However, imatinib was more effective in inducing apoptosis of neoplastic mast cells. Both patients with familial systemic mastocytosis had remarkable hematological and skin improvement after three months of imatinib treatment, suggesting that it may be an effective front line therapy for patients harboring KIT K509I mutation.
Editor: Elsevier Ltd
Rights: fechado
Identifier DOI: 10.1016/j.leukres.2014.07.010
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-84908024600&partnerID=40&md5=beaf055a96e0773ba38ebbf40f6a8203
Date Issue: 2014
Appears in Collections:Unicamp - Artigos e Outros Documentos

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