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Cited by 188

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Targeting leukemic stem cells by breaking their dormancy

Open access
Essers, Marieke Alida Gertruda, Trumpp, Andreas·2010·Molecular Oncology

Abstract

Transient or long‐term quiescence, the latter referred to as dormancy are fundamental features of at least some adult stem cells. The status of dormancy is likely a critical mechanism for the observed resistance of normal HSCs and leukemic stem cells (LSCs) to anti‐proliferative chemotherapy. Recent studies have revealed cytokines such as Interferon‐alpha (IFNα) and G‐CSF as well as arsenic trioxide (As2O3) to be efficient agents for promoting cycling of dormant HSCs and LSCs. Most interestingly, such cell cycle activated stem cells become exquisitely sensitive to killing by different chemotherapeutic agents, suggesting that dormant LSCs in patients may be targeted by a sequential two‐step protocol involving an initial activation by IFNα, G‐CSF or As2O3, followed by targeted chemotherapy.

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Crossref · 10.1016/j.molonc.2010.06.001

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Metadata

Authors
Essers, M. A. G., & Trumpp, A.
Venue
Molecular Oncology
Publisher
Wiley
Published
2010-06-09
Volume
4
Issue
5
Pages
443-450
ISSN
  • 1574-7891 (ISSN-L)
  • 1878-0261
OpenAlex
W1964505039
Cited by
188
References
5
FWCI
9.16
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Targeting leukemic stem cells by breaking their dormancy. https://app.cochat.ai/papers/10.1016/j.molonc.2010.06.001
The paper
Essers, M. A. G., & Trumpp, A. (2010). Targeting leukemic stem cells by breaking their dormancy. Molecular Oncology. https://doi.org/10.1016/j.molonc.2010.06.001

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.