SwePub
Sök i LIBRIS databas

  Utökad sökning

WFRF:(Nagy Noemi)
 

Sökning: WFRF:(Nagy Noemi) > (2020-2022) > Combination of tyro...

Combination of tyrosine kinase inhibitors and the MCL1 inhibitor S63845 exerts synergistic antitumorigenic effects on CML cells

Malyukova, Alena (författare)
Karolinska Inst, Sweden,Department of Medicine Solna, Karolinska Institute, Stockholm, Sweden
Ujvari, Dorina (författare)
Karolinska Institutet,Department of Women’s and Children’s Health, Karolinska Institute, Stockholm, Sweden
Yektaei-Karin, Elham (författare)
Karolinska Inst, Sweden,Department of Medicine Solna, Karolinska Institute, Stockholm, Sweden
visa fler...
Zovko, Ana (författare)
Karolinska Inst, Sweden,Department of Medicine Solna, Karolinska Institute, Stockholm, Sweden
Madapura, Harsha S. (författare)
Karolinska Inst, Sweden,Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden
Keszei, Marton (författare)
Karolinska Institutet,Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden
Nagy, Noemi (författare)
Karolinska Institutet,Department of Cell and Molecular Biology, Karolinska Institute, Stockholm, Sweden
Lotfi, Kourosh, 1966- (författare)
Linköpings universitet,Medicinska fakulteten,Avdelningen för klinisk kemi och farmakologi,Region Östergötland, Hematologiska kliniken US,Department of Hematology, Linköping University Hospital, Linköping, Sweden; Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden
Björn, Niclas (författare)
Linköpings universitet,Avdelningen för klinisk kemi och farmakologi,Medicinska fakulteten,Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden
Wallvik, Jonas (författare)
Umeå universitet,Avdelningen för medicin
Tamai, Minori (författare)
Univ Yamanashi, Japan,Department of Pediatrics, School of Medicine, University of Yamanashi, Chuo, Japan
Nguyen, Thao T. T. (författare)
Univ Yamanashi, Japan,Department of Pediatrics, School of Medicine, University of Yamanashi, Chuo, Japan
Akahane, Koshi (författare)
Univ Yamanashi, Japan,Department of Pediatrics, School of Medicine, University of Yamanashi, Chuo, Japan
Inukai, Takeshi (författare)
Univ Yamanashi, Japan,Department of Pediatrics, School of Medicine, University of Yamanashi, Chuo, Japan
Stenke, Leif (författare)
Karolinska Institutet,Department of Medicine Solna, Karolinska Institute, Stockholm, Sweden; Division of Hematology, Karolinska University Hospital Solna, Stockholm, Sweden
Salamon, Daniel (författare)
Karolinska Institutet,Department of Women’s and Children’s Health, Karolinska Institute, Stockholm, Sweden
visa färre...
 (creator_code:org_t)
2021-09-25
2021
Engelska.
Ingår i: Cell Death and Disease. - : Springer Nature. - 2041-4889 .- 2041-4889. ; 12:10
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Tyrosine kinase inhibitor (TKI) treatment has dramatically improved the survival of chronic myeloid leukemia (CML) patients, but measurable residual disease typically persists. To more effectively eradicate leukemia cells, simultaneous targeting of BCR-ABL1 and additional CML-related survival proteins has been proposed. Notably, several highly specific myeloid cell leukemia 1 (MCL1) inhibitors have recently entered clinical trials for various hematologic malignancies, although not for CML, reflecting the insensitivity of CML cell lines to single MCL1 inhibition. Here, we show that combining TKI (imatinib, nilotinib, dasatinib, or asciminib) treatment with the small-molecule MCL1 inhibitor S63845 exerted strong synergistic antiviability and proapoptotic effects on CML lines and CD34+ stem/progenitor cells isolated from untreated CML patients in chronic phase. Using wild-type BCR-ABL1-harboring CML lines and their T315I-mutated sublines (generated by CRISPR/Cas9-mediated homologous recombination), we prove that the synergistic proapoptotic effect of the drug combination depended on TKI-mediated BCR-ABL1 inhibition, but not on TKI-related off-target mechanisms. Moreover, we demonstrate that colony formation of CML but not normal hematopoietic stem/progenitor cells became markedly reduced upon combination treatment compared to imatinib monotherapy. Our results suggest that dual targeting of MCL1 and BCR-ABL1 activity may efficiently eradicate residual CML cells without affecting normal hematopoietic stem/progenitors.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy