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Identifying Bone Marrow Microenvironmental Populations in Myelodysplastic Syndrome and Acute Myeloid Leukemia
Published on: November 10, 2023
Primary myelofibrosis and the "bad seeds in bad soil" concept
Marie-Caroline Le Bousse-Kerdilès1
1The French INSERM and the European EUMNET networks on Myelofibrosis, The French Intergroup of Myeloproliferative disorders (FIM), INSERM U972, Paris XI University, Laboratory of Hematology, Paul Brousse Hospital, 14, av. Paul-Vaillant Couturier ; 948007, Villejuif Cedex, France.
Abstract:
Primary Myelofibrosis (PMF) is a chronic myeloproliferative neoplasm characterized by a clonal myeloproliferation and a myelofibrosis. The concomitant presence of neoangiogenesis and osteosclerosis suggests a deregulation of medullar stem cell niches in which hematopoietic stem cells are engaged in a constant crosstalk with their stromal environment. Despite the recently discovered mutations including the JAK2(Val617F) mutation, the primitive molecular event responsible for the clonal hematopoietic proliferation is still unknown. We propose that the "specificity" of the pathological process that caracterizes PMF results from alterations in the cross talk between hematopoietic and stromal cells. These alterations contribute in creating a abnormal microenvironment that participates in the maintenance of the neoplasic clone leading to a misbalance disfavouring normal hematopoiesis; in return or simultaneously, stromal cells constituting the niches are modulated by hematopoietic cells resulting in stroma dysfunctions. Therefore, PMF is a remarkable "model" in which deregulation of the stem cell niche is of utmost importance for the disease development. A better understanding of the crosstalk between stem cells and their niches should imply new therapeutic strategies targeting not only intrinsic defects in stem cells but also regulatory niche-derived signals and, consequently, hematopoietic cell proliferation.
Insights
Primary Myelofibrosis involves abnormal stem cell niche interactions, leading to neoplastic clone maintenance. Understanding this crosstalk is key for new therapies targeting stem cells and their microenvironment.
Area of Science:
- Hematology
- Oncology
- Stem Cell Biology
Background:
- Primary Myelofibrosis (PMF) is a chronic myeloproliferative neoplasm with myelofibrosis.
- Associated features include neoangiogenesis and osteosclerosis, suggesting stem cell niche deregulation.
- The initial molecular driver of clonal hematopoietic proliferation in PMF remains unidentified.
Purpose of the Study:
- To investigate the role of hematopoietic and stromal cell crosstalk in PMF pathogenesis.
- To explore how altered microenvironments contribute to neoplastic clone maintenance and hematopoiesis imbalance.
- To establish PMF as a model for understanding stem cell niche deregulation.
Main Methods:
- Analysis of the crosstalk between hematopoietic stem cells and their stromal environment in PMF.
- Investigating the molecular mechanisms underlying stem cell niche dysfunctions.
- Evaluating the impact of altered niche signaling on hematopoietic cell proliferation.
Main Results:
- Alterations in hematopoietic-stromal cell crosstalk are proposed as specific to PMF.
- These alterations create an abnormal microenvironment supporting the neoplastic clone.
- This leads to a hematopoiesis imbalance and stromal cell dysfunction.
Conclusions:
- Stem cell niche deregulation is crucial for PMF development.
- Understanding stem cell-niche interactions offers new therapeutic targets.
- Therapies could target intrinsic stem cell defects and niche-derived signals.
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