TY - JOUR
T1 - Distinct leukemogenic mechanism of acute promyelocytic leukemia based on genomic structure of PML::RAR?
AU - Minami, Mariko
AU - Sakoda, Teppei
AU - Kawano, Gentaro
AU - Kochi, Yu
AU - Sasaki, Kensuke
AU - Sugio, Takeshi
AU - Jinnouchi, Fumiaki
AU - Miyawaki, Kohta
AU - Kunisaki, Yuya
AU - Kato, Koji
AU - Miyamoto, Toshihiro
AU - Akashi, Koichi
AU - Kikushige, Yoshikane
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2025.
PY - 2025/4
Y1 - 2025/4
N2 - Leukemic stem cells (LSCs) of acute myeloid leukemia (AML) can be enriched in the CD34+CD38- fraction and reconstitute human AML in vivo. However, in acute promyelocytic leukemia (APL), which constitutes 10% of all AML cases and is driven by promyelocytic leukemia-retinoic acid receptor alpha (PML::RARα) fusion genes, the presence of LSCs has long been unidentified because of the difficulty in efficient reconstitution of human APL in vivo. Herein, we show that LSCs of the short-type isoform APL, a subtype of APL defined by different breakpoints of the PML gene, concentrate in the CD34+CD38− fraction and express T cell immunoglobulin mucin-3 (TIM-3). Short-type APL cells exhibited distinct gene expression signatures, including LSC-related genes, compared to the other types of APL. Moreover, CD34+CD38−TIM-3+ short-type APL cells efficiently reconstituted human APL in xenograft models with high penetration, whereas CD34− differentiated APL cells did not. Furthermore, CD34+CD38−TIM-3+ short-type APL cells reconstituted leukemia cells after serial transplantation. Thus, short-type APL was hierarchically organized by self-renewing APL-LSCs. The identification of LSCs in a subset of APL and establishment of an efficient patient-derived xenograft model may contribute to further understanding the APL leukemogenesis and devise individual treatments for the eradication of APL LSCs.
AB - Leukemic stem cells (LSCs) of acute myeloid leukemia (AML) can be enriched in the CD34+CD38- fraction and reconstitute human AML in vivo. However, in acute promyelocytic leukemia (APL), which constitutes 10% of all AML cases and is driven by promyelocytic leukemia-retinoic acid receptor alpha (PML::RARα) fusion genes, the presence of LSCs has long been unidentified because of the difficulty in efficient reconstitution of human APL in vivo. Herein, we show that LSCs of the short-type isoform APL, a subtype of APL defined by different breakpoints of the PML gene, concentrate in the CD34+CD38− fraction and express T cell immunoglobulin mucin-3 (TIM-3). Short-type APL cells exhibited distinct gene expression signatures, including LSC-related genes, compared to the other types of APL. Moreover, CD34+CD38−TIM-3+ short-type APL cells efficiently reconstituted human APL in xenograft models with high penetration, whereas CD34− differentiated APL cells did not. Furthermore, CD34+CD38−TIM-3+ short-type APL cells reconstituted leukemia cells after serial transplantation. Thus, short-type APL was hierarchically organized by self-renewing APL-LSCs. The identification of LSCs in a subset of APL and establishment of an efficient patient-derived xenograft model may contribute to further understanding the APL leukemogenesis and devise individual treatments for the eradication of APL LSCs.
UR - https://www.scopus.com/pages/publications/85218257991
UR - https://www.scopus.com/pages/publications/85218257991#tab=citedBy
U2 - 10.1038/s41375-025-02530-9
DO - 10.1038/s41375-025-02530-9
M3 - Article
C2 - 39979604
AN - SCOPUS:85218257991
SN - 0887-6924
VL - 39
SP - 844
EP - 853
JO - Leukemia
JF - Leukemia
IS - 4
M1 - 371
ER -