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IMMUNOLOGY2026™ Conference Recordings For Attendee ...
Mammary tumour hijacking of myelopoiesis
Mammary tumour hijacking of myelopoiesis
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Video Summary
Hannah described work showing that mammary tumors systemically reprogram the bone marrow, starting at the level of long-term hematopoietic stem cells. In both metastatic breast cancer patients and a mouse mammary tumor model (KEP), tumors caused increased circulating neutrophils with enhanced nitric oxide and ROS production, making them more suppressive of T cell proliferation and more supportive of metastasis. Single-cell and bulk RNA-seq revealed that tumor-bearing mice had more myeloid progenitors and fewer lymphoid/erythroid progenitors, with stem cells pushed toward accelerated neutrophil differentiation. IL-1β emerged as a key driver: HSPCs express IL-1R1, respond directly to IL-1β, and anti-IL-1β treatment normalized transcriptional and chromatin changes, reduced suppressive neutrophil function, and lowered lung and lymph node metastasis. The team is now testing combination therapy with checkpoint blockade in established metastatic disease.
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Date
April 19, 2026 8:00 AM - 9:30 AM
Room
153C
Session
Remember Me! - Exploration of the full spectrum of immune memory, Sponsored by the Canadian Society of Immunology (CSI)
Speaker
Hannah Garner
Track
Lymphocyte Differentiation and Peripheral Maintenance (LYM)
Year
2026
Keywords
April 19, 2026 8:00 AM - 9:30 AM
153C
Remember Me! - Exploration of the full spectrum of immune memory, Sponsored by the Canadian Society of Immunology (CSI)
Hannah Garner
Lymphocyte Differentiation and Peripheral Maintenance (LYM)
2026
mammary tumors
bone marrow reprogramming
IL-1β
neutrophils
metastasis
hematopoietic stem cells
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