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ESH CLL 2022 | The role of macrophage signals and CXCR4 in the growth of CLL cells

In this video, Dimitar Efremov, MD, PhD, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy, gives an overview on the role of signals from macrophages and the chemokine receptor CXCR4 in promoting the growth of chronic lymphocytic leukemia (CLL) cells. Using in-vivo models and CRISPR-Cas9 genome editing, Dr Efremov explains how the disruption of selective pathways in the microenvironment can influence the growth of CLL cells and provide potential therapeutic targets for the future treatment of CLL. This interview took place during the 2nd ESH Translational Research Conference on Chronic Lymphocytic Leukemia (ESH CLL), 2022.

Transcript (edited for clarity)

I will be presenting an overview on the role of signals from macrophages and from the chemokine receptor CXCR4, in promoting the growth and survival of chronic lymphocytic leukemia cells. And I will also describe some recent studies from a laboratory in which we investigated the importance of these signals in in-vivo models of chronic lymphocytic leukemia and Richter’s syndrome that were recently developed...

I will be presenting an overview on the role of signals from macrophages and from the chemokine receptor CXCR4, in promoting the growth and survival of chronic lymphocytic leukemia cells. And I will also describe some recent studies from a laboratory in which we investigated the importance of these signals in in-vivo models of chronic lymphocytic leukemia and Richter’s syndrome that were recently developed. And these models allow us to selectively inactivate various intercellular pathways that transmit signals from the micro-environment. This is done using a technique called CRISPR-Cas9 genome editing, and then investigate how destruction of these pathways will affect the growth of the leukemic cells in vivo. And the main message of my presentation is that both signals from macrophages and from the CXCR4 receptor, provide a growth advantage to the leukemic cells, and as such could represent potential therapeutic targets in chronic lymphocytic leukemia and Richter’s syndrome.

 

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