Title : The Lyn-SIRT1 signaling pathway is involved in imatinib resistance in chronic myeloid leukaemia.

Pub. Date : 2020

PMID : 32655803






4 Functional Relationships(s)
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1 In vivo experiments showed that imatinib and/or SIRT1 inhibition both prolonged the survival of the CML mouse model and that the effects of imatinib were enhanced in combination with SIRT1 inhibition. Imatinib Mesylate sirtuin 1 Mus musculus
2 CONCLUSION: We proposed a novel molecular mechanism of imatinib resistance in CML in which the high expression of Lyn in imatinib-resistant cells inhibited Ac-Foxo1 and p53 expression through the BCR-ABL/SIRT1/Foxo1 signaling pathway, thus reducing apoptosis and mediating imatinib resistance. Imatinib Mesylate sirtuin 1 Mus musculus
3 CONCLUSION: We proposed a novel molecular mechanism of imatinib resistance in CML in which the high expression of Lyn in imatinib-resistant cells inhibited Ac-Foxo1 and p53 expression through the BCR-ABL/SIRT1/Foxo1 signaling pathway, thus reducing apoptosis and mediating imatinib resistance. Imatinib Mesylate sirtuin 1 Mus musculus
4 CONCLUSION: We proposed a novel molecular mechanism of imatinib resistance in CML in which the high expression of Lyn in imatinib-resistant cells inhibited Ac-Foxo1 and p53 expression through the BCR-ABL/SIRT1/Foxo1 signaling pathway, thus reducing apoptosis and mediating imatinib resistance. Imatinib Mesylate sirtuin 1 Mus musculus