Expression and regulation of C/EBPα in normal myelopoiesis and in malignant transformation

被引:133
作者
Avellino, Roberto [1 ]
Delwel, Ruud [1 ]
机构
[1] Erasmus MC, Dept Hematol, Doctor Molewaterplein 50,3015, Rotterdam, Netherlands
关键词
ACUTE MYELOID-LEUKEMIA; BINDING-PROTEIN-ALPHA; BIALLELIC CEBPA MUTATIONS; C-JUN EXPRESSION; GENE-EXPRESSION; STEM-CELLS; GRANULOCYTIC DIFFERENTIATION; TRANSCRIPTIONAL CONTROL; CHROMATIN ARCHITECTURE; UNIPARENTAL DISOMY;
D O I
10.1182/blood-2016-09-687822
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
One of the most studied transcription factors in hematopoiesis is the leucine zipper CCAAT-enhancer binding proteina (C/EBP alpha), which is mainly involved in cell fate decisions for myeloid differentiation. Its involvement in acute myeloid leukemia (AML) is diverse, with patients frequently exhibiting mutations, deregulation of gene expression, or alterations in the function of C/EBP alpha. In this review, we emphasize the importance of C/EBP alpha for neutrophil maturation, its role in myeloid priming of hematopoietic stem and progenitor cells, and its indispensable requirement for AML development. We discuss that mutations in the open reading frame of CEBPA lead to an altered C/EBP alpha function, affecting the expression of downstream genes and consequently deregulating myelopoiesis. The emerging transcriptional mechanisms of CEBPA are discussed based on recent studies. Novel insights on howthese mechanisms may be deregulated by oncoproteins or mutations/variants in CEBPA enhancers are suggested in principal to reveal novel mechanisms of how CEBPA is deregulated at the transcriptional level.
引用
收藏
页码:2083 / 2091
页数:9
相关论文
共 117 条
[81]
THE 2 C/EBP ISOFORMS, IL-6DBP/NF-IL6 AND C/EBP-DELTA/NF-IL6-BETA, ARE INDUCED BY IL-6 TO PROMOTE ACUTE PHASE GENE-TRANSCRIPTION VIA DIFFERENT MECHANISMS [J].
RAMJI, DP ;
VITELLI, A ;
TRONCHE, F ;
CORTESE, R ;
CILIBERTO, G .
NUCLEIC ACIDS RESEARCH, 1993, 21 (02) :289-294
[82]
Elevated c-Jun expression in acute myeloid leukemias inhibits C/EBPα DNA binding via leucine zipper domain interaction [J].
Rangatia, J ;
Vangala, RK ;
Singh, SM ;
Zada, AAP ;
Elsässer, A ;
Kohlmann, A ;
Haferlach, T ;
Tenen, DG ;
Hiddemann, W ;
Behre, G .
ONCOGENE, 2003, 22 (30) :4760-4764
[83]
Downregulation of c-Jun expression by transcription factor C/EBPα is critical for granulocytic lineage commitment [J].
Rangatia, J ;
Vangala, RK ;
Treiber, N ;
Zhang, P ;
Radomska, H ;
Tenen, DG ;
Hiddemann, W ;
Behre, G .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (24) :8681-8694
[84]
Molecular mechanisms underlying deregulation of C/EBPα in acute myeloid leukemia [J].
Reckzeh, Kristian ;
Cammenga, Jorg .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2010, 91 (04) :557-568
[85]
Sarojam Santhi, 2015, Asian Pac J Cancer Prev, V16, P3785
[86]
Reintroduction of C/EBPα in leukemic CD34+ stem/progenitor cells impairs self-renewal and partially restores myelopoiesis [J].
Schepers, Hein ;
Wierenga, Albertus T. J. ;
van Gosliga, Djoke ;
Eggen, Bart J. L. ;
Vellenga, Edo ;
Schuringa, Jan Jacob .
BLOOD, 2007, 110 (04) :1317-1325
[87]
Uniparental disomy may be associated with microsatellite instability in acute myeloid leukemia (AML) with a normal karyotype [J].
Serrano, Elena ;
Carnicer, Maria J. ;
Orantes, Vanesa ;
Estivill, Camino ;
Lasa, Adriana ;
Brunet, Salut ;
Aventin, Anna M. ;
Sierra, Jorge ;
Nomdedeu, Josep F. .
LEUKEMIA & LYMPHOMA, 2008, 49 (06) :1178-1183
[88]
Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2 [J].
Snaddon, J ;
Smith, ML ;
Neat, M ;
Cambal-Parrales, M ;
Dixon-McIver, A ;
Arch, R ;
Amess, JA ;
Rohatiner, AZ ;
Lister, TA ;
Fitzgibbon, J .
GENES CHROMOSOMES & CANCER, 2003, 37 (01) :72-78
[89]
Lack of C/EBPα gene expression results in increased DNA synthesis and an increased frequency of immortalization of freshly isolated rat hepatocytes [J].
Soriano, HE ;
Kang, DC ;
Finegold, MJ ;
Hicks, MJ ;
Wang, ND ;
Harrison, W ;
Darlington, GJ .
HEPATOLOGY, 1998, 27 (02) :392-401
[90]
Mice lacking CCAAT/enhancer-binding protein-α show hyperproliferation of alveolar type II cells and increased surfactant protein mRNAs [J].
Sugahara, K ;
Iyama, KI ;
Kimura, T ;
Sano, K ;
Darlington, GJ ;
Akiba, T ;
Takiguchi, M .
CELL AND TISSUE RESEARCH, 2001, 306 (01) :57-63