Unmasking the dynamic influence of the hematopoietic niche as an oncogenic path to myeloid neoplasms evolution

ERC (European Research Council)HORIZON-ERCID: 101117339
EC Contribution
€19,114
Consortium Size
1 orgs
Start Year
2024
Summary

Although oncogenic driver mutations are found in healthy tissues sometimes at a prenatal stage, they do not often result in overt cancer. This genotype – phenotype discrepancy warrens the search for extrinsic mechanisms of cancer development and maintenance, such as aging or exposition to specific environments. Using myeloid neoplasms as a cancer model, I aim here at dissecting the hematopoietic-niche partnership at the “pre-leukemic”, “leukemic” and “post-leukemic” stage to identify innovative therapeutic strategies to prevent acute myeloid leukemia (AML) development, maintenance and recurrence. To enable experimental modelling of the bone marrow niche at different disease stages, I collected longitudinal paired stromal and hematopoietic primary patient samples, and generated physiologically-relevant in vitro and in vivo humanized models. In this proposal, I will first apply large-scale pooled genetic screening approaches to gain insights into the role of the hematopoietic-niche cellular communication processes in leukemic transformation of “pre-leukemic” clonal myeloid conditions. In the second part of the proposal, I will combine cutting-edge spatial single-cell RNA sequencing technologies with functional genetic screening to dissect the “leukemic-niche” crosstalk and ultimately fuel the development of concomitant “seeds” and “soil” therapeutic strategies. Finally, I will design a functional single-cell screening approach allowing modulation of the “post-leukemic” niche, to open the road for novel maintenance treatment strategies re-establishing healthy hematopoietic stem cells fitness advantage to prevent relapse.Overall, the proposed research project provides a framework for defining and understanding the dynamic influence of the hematopoietic niche as an oncogenic path to myeloid neoplasms evolution, and represents a key step towards therapeutic niche reprogramming from a “malignant” to a “healthy” state, to improve cancer patients’ prognosis.

Consortium (1)

Project Results (1)

Source: CORDIS, the EU research results database.

Publications (1)
Nature Communications
Nature Communications· 2025DOI
Nabih Maslah; Nina Kaci; Blandine Roux; Gabriela Alexe; Raphael Marie; Hélène Pasquer; Emmanuelle Verger; Rafael Daltro De Oliveira; Cécile Culeux; Bochra Mlayah; Nicolas Gauthier; Fanny Gonzales; Lin-Pierre Zhao; Saravanan Ganesan; Panhong Gou; Frank Ling; Juliette Soret-Dulphy; Nathalie Parquet; William Vainchenker; Emmanuel Raffoux; Rose Ann Padua; Stéphane Giraudier; Caroline Marty; Isabelle Plo; Camille Lobry; Kimberly Stegmaier; Alexandre Puissant; Jean-Jacques Kiladjian; Bruno Cassinat; Lina Benajiba