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Metabolic regulation of chemoresistance and immuno-surveillance in AML by SHP-1

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The chemoresistant and immunoevasive characteristics of leukaemia stem cells (LSCs) impede the treatment efficacy for acute myeloid leukaemia (AML). We find that inhibiting the tyrosine phosphatase SHP-1 effectively alters the metabolic state of LSCs, making them more susceptible to chemotherapy and immune surveillance in AML.

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Fig. 1: SHP-1 inhibition enhances the efficacy of chemotherapy and immune surveillance in AML.

References

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This is a summary of: Xu, X. et al. SHP-1 inhibition targets leukaemia stem cells to restore immunosurveillance and enhance chemosensitivity by metabolic reprogramming. Nat. Cell Biol. https://doi.org/10.1038/s41556-024-01349-3 (2024).

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Metabolic regulation of chemoresistance and immuno-surveillance in AML by SHP-1. Nat Cell Biol 26, 329–330 (2024). https://doi.org/10.1038/s41556-024-01350-w

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