Preview |
PDF (Original Article)
- Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
693kB |
Item Type: | Editorial |
---|---|
Title: | CEBPA mutations in AML: site matters |
Creators Name: | Bullinger, L. |
Abstract: | In this issue of Blood, based on a retrospective analysis of 4708 acute myeloid leukemia (AML) cases, Taube et al evaluate the impact of CCAAT/enhancer binding protein a (CEBPA) mutations and show that it is especially in-frame mutations affecting the basic leucine zipper region (bZIP) of CEPBA that confer a favorable outcome, irrespective of their occurrence as biallelic (CEBPAbi) or single mutation (CEBPAsm). Compared with transactivation domain (TAD) mutations, this study strongly supports a previously undefined role of CEBPA bZIP mutations, which is reflected in a distinct disease biology including younger age, higher white blood cell counts, the presence of GATA2 mutations, and high complete remission rates and long median event-free and overall survival. |
Keywords: | Acute Myeloid Leukemia, CCAAT-Enhancer-Binding Proteins, Mutation |
Source: | Blood |
ISSN: | 0006-4971 |
Publisher: | American Society of Hematology |
Volume: | 139 |
Number: | 1 |
Page Range: | 6-7 |
Date: | 6 January 2022 |
Additional Information: | Copyright © 2022 by The American Society of Hematology |
Official Publication: | https://doi.org/10.1182/blood.2021013557 |
PubMed: | View item in PubMed |
Repository Staff Only: item control page