[PDF][PDF] Estrogen signaling selectively induces apoptosis of hematopoietic progenitors and myeloid neoplasms without harming steady-state hematopoiesis

A Sánchez-Aguilera, L Arranz, D Martín-Pérez… - Cell stem cell, 2014 - cell.com
A Sánchez-Aguilera, L Arranz, D Martín-Pérez, A García-García, V Stavropoulou
Cell stem cell, 2014cell.com
Estrogens are potent regulators of mature hematopoietic cells; however, their effects on
primitive and malignant hematopoietic cells remain unclear. Using genetic and
pharmacological approaches, we observed differential expression and function of estrogen
receptors (ERs) in hematopoietic stem cell (HSC) and progenitor subsets. ERα activation
with the selective ER modulator (SERM) tamoxifen induced apoptosis in short-term HSCs
and multipotent progenitors. In contrast, tamoxifen induced proliferation of quiescent long …
Summary
Estrogens are potent regulators of mature hematopoietic cells; however, their effects on primitive and malignant hematopoietic cells remain unclear. Using genetic and pharmacological approaches, we observed differential expression and function of estrogen receptors (ERs) in hematopoietic stem cell (HSC) and progenitor subsets. ERα activation with the selective ER modulator (SERM) tamoxifen induced apoptosis in short-term HSCs and multipotent progenitors. In contrast, tamoxifen induced proliferation of quiescent long-term HSCs, altered the expression of self-renewal genes, and compromised hematopoietic reconstitution after myelotoxic stress, which was reversible. In mice, tamoxifen treatment blocked development of JAK2V617F-induced myeloproliferative neoplasm in vivo, induced apoptosis of human JAK2V617F+ HSPCs in a xenograft model, and sensitized MLL-AF9+ leukemias to chemotherapy. Apoptosis was selectively observed in mutant cells, and tamoxifen treatment only had a minor impact on steady-state hematopoiesis in disease-free animals. Together, these results uncover specific regulation of hematopoietic progenitors by estrogens and potential antileukemic properties of SERMs.
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