Modulation of Cell Differentiation, Proliferation, and Tumor Growth by Dihydrobenzyloxopyrimidine Non-Nucleoside Reverse Transcriptase Inhibitors

被引:15
作者
Sbardella, Gianluca [1 ]
Mai, Antonello [2 ]
Bartoini, Sara [3 ]
Castellano, Sabrina [1 ]
Cirilli, Roberto [3 ]
Rotili, Dante [2 ]
Milite, Ciro [1 ]
Santoriello, Marisabella [1 ]
Orlando, Serena [4 ]
Sciamanna, Ilaria [3 ]
Serafino, Annalucia [5 ]
Lavia, Patrizia [4 ]
Spadafora, Corrado [3 ]
机构
[1] Univ Salerno, Epigenet Med Chem Lab, Dipartimento Sci Farmaceut & Biomed, I-84084 Fisciano, SA, Italy
[2] Univ Roma La Sapienza, Dipartimento Chim & Tecnol Farmaco, Ist Pasteur, Fdn Cenci Bolognetti, I-00185 Rome, Italy
[3] Ist Super Sanita, I-00161 Rome, Italy
[4] Univ Roma La Sapienza, Ist Biol Mol & Patol, CNR, I-00185 Rome, Italy
[5] CNR, Ist Farmacol Traslaz, I-00133 Rome, Italy
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; ANTI-HIV-1; ACTIVITY; IN-VITRO; GENOME EVOLUTION; 3,4-DIHYDRO-2-ALKOXY-6-BENZYL-4-OXOPYRIMIDINES DABOS; PROMOTES DIFFERENTIATION; CARCINOMA-CELLS; BREAST-CANCER; POTENT; RETROTRANSPOSONS;
D O I
10.1021/jm200734j
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of 5-alkyl-2-(alkylthio)-6-(1-(2,6-difluorophenyl)propyl)-3,4-dihydropyrimidin-4(3H)-one derivatives (3a-h) belonging to the F-2-DABOs class of non-nucleoside HIV-1 reverse transcriptase inhibitors (NNRTIs) are endowed with a strong antiproliferative effect and induce cytodifferentiation in A375 melanoma cells. Among tested compounds, the most potent is 3g (SPV122), which also induces apoptosis in a cell-density-dependent manner and antagonizes tumor growth in animal models. All these effects are similar or even more pronounced than those previously reported for other nucleoside or non-nucleoside inhibitors of reverse transcriptase or by functional knockout of the reverse-transcriptase-encoding long interspersed element 1 by RNA interference (RNAi). Taken together with our previously reported results, these data further confirm our idea that cellular alterations induced by NNRTIs are a consequence of the inhibition of the endogenous reverse transcriptase in A375 cells and support the potential of NNRTIs as valuable agents in cancer therapy.
引用
收藏
页码:5927 / 5936
页数:10
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