- Title
- Small molecule inhibition of Dynamin-dependent endocytosis targets multiple niche signals and impairs leukemia stem cells
- Creator
- Tremblay, Cedric S.; Chiu, Sung Kai; Saw, Jesslyn; McCalmont, Hannah; Litalien, Veronique; Boyle, Jacqueline; Sonderegger, Stefan E.; Chau, Ngoc; Evans, Kathryn; Cerruti, Loretta; Salmon, Jessica M.; McCluskey, Adam; Lock, Richard B.; Robinson, Phillip J.; Jane, Stephen M.; Curtis, David J.
- Relation
- Nature Communications Vol. 11, Issue 1, no. 6211
- Publisher Link
- http://dx.doi.org/10.1038/s41467-020-20091-6
- Publisher
- Nature Publishing Group
- Resource Type
- journal article
- Date
- 2020
- Description
- Intensive chemotherapy for acute leukemia can usually induce complete remission, but fails in many patients to eradicate the leukemia stem cells responsible for relapse. There is accumulating evidence that these relapse-inducing cells are maintained and protected by signals provided by the microenvironment. Thus, inhibition of niche signals is a proposed strategy to target leukemia stem cells but this requires knowledge of the critical signals and may be subject to compensatory mechanisms. Signals from the niche require receptor-mediated endocytosis, a generic process dependent on the Dynamin family of large GTPases. Here, we show that Dynole 34-2, a potent inhibitor of Dynamin GTPase activity, can block transduction of key signalling pathways and overcome chemoresistance of leukemia stem cells. Our results provide a significant conceptual advance in therapeutic strategies for acute leukemia that may be applicable to other malignancies in which signals from the niche are involved in disease progression and chemoresistance.
- Subject
- Dynamin-dependent endocytosis; chemotherapy; acute leukemia; Dynole 34-2; Dynamin GTPase; stem cells; SDG 3; Sustainable Development Goals
- Identifier
- http://hdl.handle.net/1959.13/1438389
- Identifier
- uon:40592
- Identifier
- ISSN:2041-1723
- Language
- eng
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