Enhanced p73 expression during differentiation and complex p73 isoforms in myeloid leukemia

被引:47
作者
Tschan, MP
Grob, TJ
Peters, UR
De Laurenzi, V
Huegli, B
Kreuzer, KA
Schmidt, CA
Melino, G
Fey, MF
Tobler, A
Cajot, JF
机构
[1] Univ Bern, Dept Clin Res, Inst Med Oncol, Cent Hematol Lab, CH-3010 Bern, Switzerland
[2] Univ Bern, Inselspital, CH-3010 Bern, Switzerland
[3] Humboldt Univ, Charite Virchow Clin, Dept Hematol Oncol, Berlin, Germany
[4] Univ Roma Tor Vergata, Dept Expt Med, Rome, Italy
关键词
p73; myeloid differentiation; leukemia; AML; CML;
D O I
10.1006/bbrc.2000.3627
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 p53 homologue p73 is expressed in at least six different isoforms (alpha, beta, gamma, delta, epsilon, and zeta), but unlike p53 it has rarely been found mutated in human cancers. However, altered expression of this gene has been reported in cancer cells. In order to understand if p73 is involved in normal and malignant development of myeloid cells, we investigated the expression pattern of the different p73 isoforms in progenitor and mature normal myeloid cells as well as in cells derived from acute and chronic myeloid leukemias. The results show that expression of p73 is markedly enhanced during differentiation of myeloid leukemic cells and that leukemic blasts from patients show an increased expression of the shorter p73 isoforms (gamma, delta, epsilon, zeta). In particular the epsilon isoform is only expressed in leukemic cells and completely absent in mature myeloid cells. Altogether our data suggest that p73 is involved in myeloid differentiation and its altered expression is involved in leukemic degeneration. (C) 2000 Academic Press.
引用
收藏
页码:62 / 65
页数:4
相关论文
共 20 条
[1]  
Agami R, 1999, NATURE, V399, P809
[2]   Induction of neuronal differentiation by p73 in a neuroblastoma cell line [J].
De Laurenzi, V ;
Raschellá, G ;
Barcaroli, D ;
Annicchiarico-Petruzzelli, M ;
Ranalli, M ;
Catani, MV ;
Tanno, B ;
Costanzo, A ;
Levrero, M ;
Melino, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (20) :15226-15231
[3]   Additional complexity in p73:: induction by mitogens in lymphoid cells and identification of two new splicing variants ε and ζ [J].
De Laurenzi, V ;
Catani, MV ;
Terrinoni, A ;
Corazzari, M ;
Melino, G ;
Costanzo, A ;
Levrero, M ;
Knight, RA .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (05) :389-390
[4]   Two new p73 splice variants, γ and δ, with different transcriptional activity [J].
De Laurenzi, V ;
Costanzo, A ;
Barcaroli, D ;
Terrinoni, A ;
Falco, M ;
Annicchiarico-Petruzzeli, M ;
Levrero, M ;
Melino, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (09) :1763-1768
[5]  
Gong JG, 1999, NATURE, V399, P806
[6]   p53 family genes: structural comparison, expression and mutation [J].
Ikawa, S ;
Nakagawara, A ;
Ikawa, Y .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (12) :1154-1161
[7]   The p53 gene family [J].
Kaelin, WG .
ONCOGENE, 1999, 18 (53) :7701-7705
[8]   Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers [J].
Kaghad, M ;
Bonnet, H ;
Yang, A ;
Creancier, L ;
Biscan, JC ;
Valent, A ;
Minty, A ;
Chalon, P ;
Lelias, JM ;
Dumont, X ;
Ferrara, P ;
McKeon, F ;
Caput, D .
CELL, 1997, 90 (04) :809-819
[9]   Regulation and activation of p53 and its family members [J].
Lohrum, MAE ;
Vousden, KH .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (12) :1162-1168
[10]  
Peters UR, 1999, CANCER RES, V59, P4233