Accumulation of γ-globin mRNA in human erythroid cells treated with angelicin

被引:86
作者
Lampronti, I
Bianchi, N
Borgatti, M
Fibach, E
Prus, E
Gambari, R
机构
[1] Univ Ferrara, Dept Biochem & Mol Biol, I-44100 Ferrara, Italy
[2] Hadassah Univ Hosp, Dept Hematol, IL-91120 Jerusalem, Israel
[3] Ctr Biotechnol, Lab Dev Pharmacol & Pharmacogenom Therapy Thalass, Ferrara, Italy
关键词
angelicin; erythroid differentiation; gamma-globin; fetal hemoglobin; beta-thalassemia; sickle cell anemia;
D O I
10.1034/j.1600-0609.2003.00113.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the present study was to determine whether angelicin is able to increase the expression of gamma-globin genes in human erythroid cells. Angelicin is structurally related to psoralens, a well-known chemical class of photosensitizers used for their antiproliferative activity in treatment of different skin diseases (i.e., psoriasis and vitiligo). To verify the activity of angelicin, we employed two experimental cell systems, the human leukemic K562 cell line and the two-phase liquid culture of human erythroid progenitors isolated from normal donors. The results of our investigation suggest that angelicin, compared with cytosine arabinoside, mithramycin and cisplatin, is a powerful inducer of erythroid differentiation and gamma-globin mRNA accumulation of human leukemia K562 cells. In addition, when normal human erythroid precursors were cultured in the presence of angelicin, increases of gamma-globin mRNA accumulation and fetal hemoglobin (HbF) production, even higher than those obtained using hydroxyurea, were detected. These results could have practical relevance, as pharmacologically-mediated regulation of the expression of human gamma-globin genes, leading to HbF induction, is considered a potential therapeutic approach in hematological disorders, including beta-thalassemia and sickle cell anemia.
引用
收藏
页码:189 / 195
页数:7
相关论文
共 37 条
[1]  
ALKHATTI A, 1988, BLOOD, V72, P817
[2]   Accumulation of γ-globin mRNA and induction of erythroid differentiation after treatment of human leukaemic K562 cells with tallimustine [J].
Bianchi, N ;
Chiarabelli, C ;
Borgatti, M ;
Mischiati, C ;
Fibach, E ;
Gambari, R .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (04) :951-961
[3]   Induction of erythroid differentiation of human K562 cells by cisplatin analogs [J].
Bianchi, N ;
Ongaro, F ;
Chiarabelli, C ;
Gualandi, L ;
Mischiati, C ;
Bergamini, P ;
Gambari, R .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (01) :31-40
[4]   The DNA-binding drugs mithramycin and chromomycin are powerful inducers of erythroid differentiation of human K562 cells [J].
Bianchi, N ;
Osti, F ;
Rutigliano, C ;
Corradini, FG ;
Borsetti, E ;
Tomassetti, M ;
Mischiati, C ;
Feriotto, G ;
Gambari, R .
BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (02) :258-265
[5]   ANGELICINS, ANGULAR ANALOGS OF PSORALENS - CHEMISTRY, PHOTOCHEMICAL, PHOTOBIOLOGICAL AND PHOTOTHERAPEUTIC PROPERTIES [J].
BORDIN, F ;
DALLACQUA, F ;
GUIOTTO, A .
PHARMACOLOGY & THERAPEUTICS, 1991, 52 (03) :331-363
[6]  
Bordin F, 1998, PHOTOCHEM PHOTOBIOL, V68, P157, DOI 10.1562/0031-8655(1998)068<0157:PPOTT>2.3.CO
[7]  
2
[8]  
CHARACHE S, 1992, BLOOD, V79, P2555
[9]   Synthesis and biological activity of (Hydroxymethyl)- and (diethylaminomethyl)benzopsoralens [J].
Chilin, A ;
Marzano, C ;
Guiotto, A ;
Manzini, P ;
Baccichetti, F ;
Carlassare, F ;
Bordin, F .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (15) :2936-2945
[10]   Antiproliferative activity and phototoxicity of some methyl derivatives of 5-methoxypsoralen and 5-methoxyangelicin [J].
Conconi, MT ;
Montesi, F ;
Parnigotto, PP .
PHARMACOLOGY & TOXICOLOGY, 1998, 82 (04) :193-198