Antiproliferative activity of new 1-aryl-4-amino-1H-pyrazolo[3,4-d]pyrimidine derivatives toward the human epidermoid carcinoma A431 cell line

被引:71
作者
Schenone, S
Bruno, O
Bondavalli, F
Ranise, A
Mosti, L
Menozzi, G
Fossa, P
Donnini, S
Santoro, A
Ziche, M
Manetti, F
Botta, M
机构
[1] Univ Genoa, Dipartimento Sci Farmaceut, I-16132 Genoa, Italy
[2] Univ Siena, Dipartimento Biol Mol, Sez Farmacol, I-53100 Siena, Italy
[3] Univ Siena, Dipartimento Farmaco Chimico Tecnol, I-53100 Siena, Italy
关键词
pyrazolo-pyrimidine; antiproliferative activity; tyrosine kinase; A431; cells;
D O I
10.1016/j.ejmech.2004.07.010
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Synthesis and biological evaluation of a new class of 1-aryl-4-amino-1H-pyrazolo[3,4-d]pyrimidine derivatives are reported. A preliminary cellular assay system using the tumor cell line A431 responding to epidermal growth factor (EGF) for its growth, shows that the new compounds are potent inhibitors of cell growth. The inhibition of tumor cell proliferation is not associated with blockage of EGF receptor (EGFR), but substantially due to the interference with the signalling pathway at the level of Src tyrosine kinase and at the level of the downstream effector signal mitogen activated protein kinases (MAPKs), ERK1-2. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:939 / 946
页数:8
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