Clonal selection in xenografted TAM recapitulates the evolutionary process of myeloid leukemia in Down syndrome

Author:

Saida Satoshi1,Watanabe Ken-ichiro1,Sato-Otsubo Aiko2,Terui Kiminori3,Yoshida Kenichi2,Okuno Yusuke2,Toki Tsutomu3,Wang RuNan3,Shiraishi Yuichi4,Miyano Satoru4,Kato Itaru1,Morishima Tatsuya1,Fujino Hisanori1,Umeda Katsutsugu1,Hiramatsu Hidefumi1,Adachi Souichi5,Ito Etsuro3,Ogawa Seishi2,Ito Mamoru6,Nakahata Tatsutoshi7,Heike Toshio1

Affiliation:

1. Department of Pediatrics, Graduate School of Medicine, Kyoto University, Kyoto, Japan;

2. Cancer Genomics Project, Graduate School of Medicine, University of Tokyo, Tokyo, Japan;

3. Department of Pediatrics, Graduate School of Medicine, Hirosaki University, Hirosaki, Japan;

4. Laboratory of DNA Information Analysis, Human Genome Center, Institute of Medical Science, University of Tokyo, Tokyo, Japan;

5. Department of Human Health Sciences, Graduate School of Medicine, Kyoto University, Kyoto, Japan;

6. Laboratory Animal Research Department, Central Institute for Experimental Animals, Kawasaki, Japan; and

7. Department of Clinical Application, Center for iPS Cell Research and Application, Kyoto University, Kyoto, Japan

Abstract

Key Points Genetically heterogeneous subclones with varying leukemia-initiating potential exist in neonatal transient abnormal myelopoiesis. This novel xenograft model of transient abnormal myelopoiesis may provide unique insight into the evolutionary process of leukemia.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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