Kinetics of ERK1/2 activation determine sensitivity of acute myeloid leukaemia cells to the induction of apoptosis by the novel small molecule ingenol 3-angelate (PEP005)

被引:15
作者
Hampson, Peter [1 ]
Wang, Keqing [1 ]
Milverton, Lisa [1 ]
Ersvaer, Elisabeth [2 ]
Bruserud, Oystein [2 ]
Lord, Janet M. [1 ]
机构
[1] Univ Birmingham, Sch Med, MRC Ctr Immune Regulat, Sch Immun & Infect, Birmingham B15 2TT, W Midlands, England
[2] Haukeland Hosp, Sect Haematol, Dept Med, N-5021 Bergen, Norway
关键词
Acute myeloid leukaemia; ERK1/2; PKC; Apoptosis; PROTEIN-KINASE-C; EPIDERMAL-GROWTH-FACTOR; EARLY GENE-PRODUCTS; PC12; CELLS; CONSTITUTIVE ACTIVATION; PHEOCHROMOCYTOMA CELLS; SIGNALING PATHWAYS; DEATH; DIFFERENTIATION; TRANSCRIPTION;
D O I
10.1007/s10495-010-0507-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The novel small molecule ingenol 3-angelate (PEP005) has been shown previously to induce apoptosis in leukaemic cell lines and primary AML cells, an effect that requires the expression of protein kinase C-delta (PKC delta). Here we have investigated signalling events downstream of PKC delta that determine sensitivity of AML cells to PEP005. We show that activation of ERK1/2 MAP kinase occurred in both sensitive and resistant cells and that induction of apoptosis required sustained signalling through the ERK1/2 pathway. Inhibition of ERK1/2 signalling using the MEK inhibitor PD98059 inhibited PEP005-induced apoptosis and activation of ERK1/2 was shown to occur downstream of PKC activation. The data show that PEP005-induced apoptosis is both PKC and ERK1/2 dependent and indicate that chronic activation of ERK1/2 in leukaemic cells delivers a pro-apoptotic rather than a proliferative or survival signal.
引用
收藏
页码:946 / 955
页数:10
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