Targeting the TLR pathway with BTK inhibitors in WM

Steven Treon
Professor Steven Treon outlines the impact of the MYD88L265P mutation on the toll-like receptor (TLR) signalling pathway and explains how Bruton's tyrosine kinase (BTK) inhibitors can be used to target the pathway.

Professor Steven Treon outlines the impact of the MYD88L+r^! mutation on the toll-like receptor (TLR) signalling pathway. Prof Treon describes the downstream consequences of the MYD88)G-{Q mutation including that it leads to NFĸB signalling which has implications for growth and survival of malignant B-cells. He also explains pHCK promotes pro-survival signalling in MYD88-mutated B-cells. He explains how Bruton’s tyrosine kinase (BTK) inhibitors can be used to target the pathway in B-cell lymphomas like Waldenström’s macroglobulinemia (WM).

4eM*LC1

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