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Hugues, P.

Publications and source records attributed to Hugues, P..

2 recordsLinked to original sources

miR-495-3p Sensitizes BCR::ABL1 Expressing Leukemic cells to Tyrosine Kinase Inhibitors by Targeting Multidrug Resistance 1 Gene including in T315I Mutated cells

Chronic myeloid leukemia (CML) is a clonal hematopoietic malignancy driven by the BCR::ABL1 fusion oncoprotein. The development of tyrosine kinase inhibitors (TKIs) has deeply increased long-term survival of CML patients. Nonetheless, one patient out of four will switch TKI off owing either to drug intolerance or resistance partly due to amplification or mutations of BCR::ABL1 oncogene and alteration of ATP-binding cassette (ABC) transporters. Increasing evidence suggests an involvement of the microRNA miR-495-3p in cancer-associated chemo-resistance through multidrug resistance 1 (MDR1) gene which encodes an ATP-dependent efflux pump. Our study aimed at investigating the potential role of miR-495-3p in CML TKI chemo-sensitivity and determining the underlying molecular circuitry involved. We first observed that miR-495-3p expression was lower in BCR::ABL1 expressing cellular models in vitro. Notably, loss-of-function experiments showed increased proliferation associated with a decreased number of non-dividing cells (G0/G1) and resistance to Imatinib. Conversely, our data showed that miR-495-3p overexpression hindered leukemic cell growth and TKI resistance even in Imatinib-resistant T315I-mutant cells as well as drug efflux activity through MDR1 regulation. To further investigate the role of miR-495-3p in CML patients, we found that predicted miR-495-3p targets were upregulated in patients in blast crisis involved in protein phosphorylation and associated with the worst prognosis. Taken together, our results demonstrate that down-regulation of miR-495-3p expression is important in the malignant phenotype of CML and TKI resistance mechanisms, which could be a useful biomarker and a potential therapeutic target to eradicate CML. MeSH termsO_LIATP Binding Cassette Transporter, Subfamily B C_LIO_LIATP Binding Cassette Transporter, Subfamily B, Member 1 / drug effects C_LIO_LIATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism* C_LIO_LIBlast Crisis / pathology C_LIO_LICell Line, Tumor C_LIO_LICell Proliferation / drug effects* C_LIO_LICell Survival / drug effects C_LIO_LIDrug Resistance C_LIO_LIGenes, MDR C_LIO_LIImatinib Mesylate C_LIO_LILeukemia, Myelogenous, Chronic, BCR-ABL Positive C_LIO_LIMicroRNAs / genetics C_LIO_LIMicroRNAs / physiology* C_LI HIGHLIGHTSO_LImiR-495-3p inhibits leukemic cell growth and is downregulated in BCR::ABL1 expressing cell lines C_LIO_LImiR-495-3p modulates response to TKI treatment including in UT7 cells expressing T315I C_LIO_LIOverexpression of miR-495-3p leads to a decrease of MDR1 and drug efflux activity C_LIO_LIBioinformatics analyses reveal that MiR-495-3p target genes are upregulated in blast crisis C_LI

cancer biology↗

Evidence of massive leukemic progenitor expansion in blood during molecular recurrence after TKI discontinuation in chronic myeloid leukemia (CML)

Chronic myeloid leukemia (CML) represents one of the major success stories of targeted therapies of the 21st century with the use of tyrosine kinase inhibitors (TKIs). Following discontinuation of TKIs in deep molecular remission context, at least half of the patients experience molecular relapse. Cellular events occurring during this phase are not yet established. In this work, we show a massive amplification of clonogenic progenitors or CFCs (colony-forming cells) in the peripheral blood of patients in molecular recurrence after a TKI discontinuation. We demonstrate, by qRT-PCR analysis on individual and pooled CFCs, that leukemic clonogenic progenitor expansion in the peripheral blood represents the first cellular event before any evidence of cytological change. These findings also suggest that the amplification of the leukemic clone during the first stages of CML takes place not only in the bone marrow but also in the peripheral blood.

cancer biology↗