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One more stem cell niche: how the sensitivity of chronic myeloid leukemia cells to imatinib mesylate is modulated within a "hypoxic" environment

Authors Rovida E, Marzi I, Cipolleschi MG, Sbarba P

Received 21 October 2013

Accepted for publication 10 December 2013

Published 21 January 2014 Volume 2014:2 Pages 1—10

DOI https://doi.org/10.2147/HP.S51812

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 5


Elisabetta Rovida, Ilaria Marzi, Maria Grazia Cipolleschi, Persio Dello Sbarba

Dipartimento di Scienze Biomediche Sperimentali e Cliniche, Università degli Studi di Firenze, Florence, Italy; Istituto Toscano Tumori, Florence, Italy

Abstract: This is a review (by no means comprehensive) of how the stem cell niche evolved from an abstract concept to a complex system, implemented with a number of experimental data at the cellular and molecular levels, including metabolic cues, on which we focused in particular. The concept was introduced in 1978 to model bone marrow sites suited to host hematopoietic stem cells (HSCs) and favor their self-renewal, while restraining clonal expansion and commitment to differentiation. Studies of the effects of low oxygen tension on HSC maintenance in vitro led us to hypothesize niches were located within bone marrow areas where oxygen tension is lower than elsewhere. We named these areas hypoxic stem cell niches, although a low oxygen tension is to be considered physiological for the environment where HSCs are maintained. HSCs were later shown to have the option of cycling in low oxygen, which steers this cycling to the maintenance of stem cell potential. Cell subsets capable of withstanding incubation in very low oxygen were also detected within leukemia cell populations, including chronic myeloid leukemia (CML). The oncogenetic Bcr/Abl protein is completely suppressed in these subsets, whereas Bcr/Abl messenger ribonucleic acid is not, indicating that CML cells resistant to low oxygen are independent of Bcr/Abl for persistence in culture but remain genetically leukemic. Accordingly, leukemia stem cells of CML selected in low oxygen are refractory to the Bcr/Abl inhibitor imatinib mesylate. Bcr/Abl protein suppression turned out to be actually determined when glucose shortage complicated the effects of low oxygen, indicating that ischemia-like conditions are the driving force of leukemia stem cell refractoriness to imatinib mesylate. These studies pointed to “ischemic” stem cell niches as a novel scenario for the maintenance of minimal residual disease of CML. A possible functional relationship of the “ischemic” with the “hypoxic” stem cell niche is discussed.

Keywords: hypoxia, ischemia, chronic myeloid leukemia, stem cell niche, leukemia stem cell, drug resistance

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