4.7 Article

Palbociclib promotes the antitumor activity of Venetoclax plus Azacitidine against acute myeloid leukemia

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 153, 期 -, 页码 -

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.113527

关键词

AML; CDK6; Palbociclib; Venetoclax; Azacitidine; BCL-2; MCL-1; BCL-X

资金

  1. National Natural Science Foundation of China [81600107, 82100230]
  2. Anhui Provincial Natural Science Foundation [1708085MH180]
  3. Fundamental Research Funds for the Central Universities [WK9110000168]
  4. Research Fund for the Key Laboratory of Anhui Province [KLICD-2022-Z2]

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The study found that the combination of the CDK6 inhibitor Palbociclib with Venetoclax/Azacitidine can improve treatment efficacy in AML patients; experimental results show that Palbociclib can increase the apoptosis rate of AML cells and make the cells more sensitive to Venetoclax/Azacitidine treatment.
Around 70 % of patients diagnosed with acute myeloid leukemia (AML) survive less than 5 years due to drug resistance and disease relapse. Consequently, improved clinical treatments are urgently needed. Some but not all AML patients benefit from the combination of the BCL-2 inhibitor Venetoclax with the hypomethylation agent Azacitidine. Here we investigated the utility of employing the cyclin dependent kinase (CDK6) inhibitor Palbociclib to improve the efficacy of Venetoclax/Azacitidine combination therapy. Our analysis of publicly available RNA sequencing datasets showed CDK6 was highly expressed in the major acute forms of leukemia including AML. Consistently, using qPCR and flow cytometry we found that CDK6 was overexpressed in bone marrow mononuclear cells from AML patients compared to healthy controls. Subsequent in vitro testing of Palbociclib, Venetoclax and Azacitidine, alone and in combination against CDK6-overexpressing AML cells lines THP-1 and KG-1 and primary AML cells showed that the Palbociclib/Venetoclax/Azacitidine combination improved treatment efficacy compared to Venetoclax/Azacitidine treatment alone. Additional investigations in a subcutaneous KG-1 mouse model showed similarly the three-drug combination produced the most significant reductions in tumor load together with the least amount of spleen infiltration. We established Palbociclib functioned in combination with Venetoclax/Azacitidine by increasing the rates of apoptosis in AML cells. Further investigations revealed that Palbociclib does not affect BCL-2 activity but downregulated the anti-apoptotic proteins MCL-1 and BCL-X-L, making AML cells more sensitive to Venetoclax/Azacitidine treatment. Our results propose that the Palbociclib/Venetoclax/Azacitidine regimen warrants further preclinical research for clinical application in AML patients.

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