Protein kinase C θ (PKCθ) expression and constitutive activation in gastrointestinal stromal tumors (GISTs)

被引:91
作者
Duensing, A
Joseph, NE
Medeiros, F
Smith, F
Hornick, JL
Heinrich, MC
Corless, CL
Demetri, GD
Fletcher, CDM
Fletcher, JA
机构
[1] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Oregon Hlth & Sci Univ, Dept Med, OHSU Canc Inst, Portland, OR USA
[3] Portland VA Med Ctr, Portland, OR USA
[4] Oregon Hlth & Sci Univ, Dept Pathol, Portland, OR USA
[5] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
基金
中国国家自然科学基金;
关键词
D O I
10.1158/0008-5472.CAN-04-0559
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
KIT expression is a key diagnostic feature of gastrointestinal stromal tumors (GISTs), and virtually all of the GISTs express oncogenic forms of the KIT or PDGFRA receptor tyrosine kinase proteins, which serve as therapeutic targets of imatinib mesylate (Gleevec; Novartis, Basel, Switzerland). However, KIT expression can be low in PDGFRA-mutant GISTs, increasing the likelihood of misdiagnosis as other types of sarcoma. We report that the signaling intermediate protein kinase C theta (PKCtheta) is a diagnostic marker in GISTs, including those that lack KIT expression and/or contain PDGFRA mutations. PKCtheta is strongly activated in most GISTs and hence may serve, along with KIT/PDGFRA, as a novel therapeutic target.
引用
收藏
页码:5127 / 5131
页数:5
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