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Discovery of survival factor for primitive chronic myeloid leukemia cells using induced pluripotent stem cells.


ABSTRACT: A definitive cure for chronic myeloid leukemia (CML) requires identifying novel therapeutic targets to eradicate leukemia stem cells (LSCs). However, the rarity of LSCs within the primitive hematopoietic cell compartment remains a major limiting factor for their study in humans. Here we show that primitive hematopoietic cells with typical LSC features, including adhesion defect, increased long-term survival and proliferation, and innate resistance to tyrosine kinase inhibitor (TKI) imatinib, can be generated de novo from reprogrammed primary CML cells. Using CML iPSC-derived primitive leukemia cells, we discovered olfactomedin 4 (OLFM4) as a novel factor that contributes to survival and growth of somatic lin(-)CD34(+) cells from bone marrow of patients with CML in chronic phase, but not primitive hematopoietic cells from normal bone marrow. Overall, this study shows the feasibility and advantages of using reprogramming technology to develop strategies for targeting primitive leukemia cells.

SUBMITTER: Suknuntha K 

PROVIDER: S-EPMC5003778 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature

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Discovery of survival factor for primitive chronic myeloid leukemia cells using induced pluripotent stem cells.

Suknuntha Kran K   Ishii Yuki Y   Tao Lihong L   Hu Kejin K   McIntosh Brian E BE   Yang David D   Swanson Scott S   Stewart Ron R   Wang Jean Y J JYJ   Thomson James J   Slukvin Igor I  

Stem cell research 20151031 3


A definitive cure for chronic myeloid leukemia (CML) requires identifying novel therapeutic targets to eradicate leukemia stem cells (LSCs). However, the rarity of LSCs within the primitive hematopoietic cell compartment remains a major limiting factor for their study in humans. Here we show that primitive hematopoietic cells with typical LSC features, including adhesion defect, increased long-term survival and proliferation, and innate resistance to tyrosine kinase inhibitor (TKI) imatinib, can  ...[more]

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