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PMID: 14592978 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

C/EBPbeta: a major PML-RARA-responsive gene in retinoic acid-induced differentiation of APL cells.

The EMBO journal ·Vol. 22 ·No. 21 ·2003-11-03 ·页码 5806-16

Duprez E, Wagner K, Koch H, Tenen DG

Abstract

In acute promyelocytic leukemia (APL), the translocation t(15;17) induces a block at the promyelocytic stage of differentiation in an all-trans-retinoic acid (ATRA)-responsive manner. Here we report that upon treatment with ATRA, t(15;17) cells (NB4) reveal a very rapid increase in protein level and binding activity of C/EBPbeta, a C/EBP family member, which was not observed in an ATRA-resistant NB4 cell line. We further provide evidence that ATRA mediates a direct increase of C/EBPbeta, only in PML-RARA (promyelocytic leukemia-retinoic acid receptor alpha)-expressing cells. In addition, transactivation experiments indicate that the PML-RARA fusion protein, but not PML-RARA mutants defective in transactivation, strongly transactivates the C/EBPbeta promoter. These results suggest that PML-RARA mediates ATRA-induced C/EBPbeta expression. Finally, we demonstrate the importance of C/EBPbeta in granulocytic differentiation. We show that not only does C/EBPbeta induce granulocytic differentiation of non-APL myeloid cell lines independent of addition of ATRA or other cytokines, but also that C/EBPbeta induction is required during ATRA-induced differentiation of APL cells. Taken together, C/EBPbeta is an ATRA-dependent PML-RARA target gene involved in ATRA-induced differentiation of APL cells.

MeSH 主题词
Base Sequence CCAAT-Enhancer-Binding Protein-beta/genetics Cell Differentiation/drug effects Gene Expression Regulation, Neoplastic/drug effects Hematopoiesis Humans K562 Cells Leukemia, Promyelocytic, Acute/genetics,metabolism,pathology Mutation Neoplasm Proteins/genetics,metabolism Oncogene Proteins, Fusion/genetics,metabolism RNA, Messenger/genetics,metabolism RNA, Neoplasm/genetics,metabolism Tretinoin/pharmacology Tumor Cells, Cultured U937 Cells
化学物质
CCAAT-Enhancer-Binding Protein-beta Neoplasm Proteins Oncogene Proteins, Fusion RNA, Messenger RNA, Neoplasm promyelocytic leukemia-retinoic acid receptor alpha fusion oncoprotein Tretinoin
作者与单位
共 4 位作者,点击展开单位 / ORCID
Duprez Estelle
Harvard Institutes of Medicine, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA. [email protected]
Wagner Katharina
Koch Heike
Tenen Daniel G
Article Info
Journal
The EMBO journal
Abbr.
EMBO J
ISSN
0261-4189
Corresponding email
Published
2003-11-03
页码
5806-16
Language
English
Country/Region
England
NLM ID
8208664
基金资助
NCI NIH HHS · P01 CA066996 · United States
NHLBI NIH HHS · R01 HL056745 · United States
NCI NIH HHS · CA66996 · United States
NHLBI NIH HHS · HL56745 · United States
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