4.3 Article

Deregulated expression of Kruppel-like factors in acute myeloid leukemia

期刊

LEUKEMIA RESEARCH
卷 35, 期 7, 页码 909-913

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.leukres.2011.03.010

关键词

Kruppel-like factors; KLF2; KLF3; KLF5; KLF6; Acute myeloid leukemia (AML); Acute promyelocytic leukemia; All-trans retinoic acid (ATRA); Neutrophil

资金

  1. Swiss National Science Foundation [3100-067213]
  2. Marlies-Schwegler Foundation
  3. Ursula-Hecht-Foundation for Leukemia Research
  4. Bernese Foundation of Cancer Research
  5. Werner and Hedy Berger-Janser Foundation of Cancer Research
  6. Bern University Research Foundation
  7. Swiss Federation Against Cancer/Oncosuisse [OCS-01823-02-2006]

向作者/读者索取更多资源

The known participation of Kruppel-like transcription factors (KLF) in cellular differentiation prompted us to investigate their expression in acute myeloid leukemia (AML) blast cells that are typically blocked in their differentiation. We determined the expression patterns of KLFs with a putative role in myeloid differentiation in a large cohort of primary AML patient samples, CD34(+) progenitor cells and granulocytes from healthy donors. We found that KLF2, KLF3, KLF5 and KLF6 are significantly lower expressed in AML blast and CD34(+) progenitor cells as compared to normal granulocytes. Moreover, we found markedly increased KLF levels in acute promyelocytic leukemia patients who received oral ATRA. Accordingly, we observed a strong induction of KLF5/6 upon ATRA-treatment in NB4 and HT93 APL but not in ATRA-resistant NB4-R cells. Lastly, knocking down KLF5 or KLF6 in NB4 cells significantly attenuated neutrophil differentiation. In conclusion, we found a significant repression of KLF transcription factors in primary AML samples as compared to mature neutrophils and further show that KLF5 and KLF6 are functionally involved in neutrophil differentiation of APL cells. (C) 2011 Elsevier Ltd. All rights reserved.

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