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. 2024 Jan 16;51(1):108.
doi: 10.1007/s11033-023-09135-4.

"Combination treatments of imatinib with astaxanthin and crocin efficiently ameliorate antioxidant status, inflammation and cell death progression in imatinib-resistant chronic myeloid leukemia cells"

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"Combination treatments of imatinib with astaxanthin and crocin efficiently ameliorate antioxidant status, inflammation and cell death progression in imatinib-resistant chronic myeloid leukemia cells"

Amin Golestani et al. Mol Biol Rep. .

Abstract

Background: Imatinib resistance remains a major obstacle in the treatment of chronic myelogenous leukemia (CML). Crocin (CRC) and astaxanthin (ATX) are phytochemicals with anti-cancer properties.

Aims: This study aimed to explore the effects of combination treatment of Imatinib with CRC and ATX on Imatinib-resistant K562 (IR-K562) cells.

Methods and results: After the establishment of IR-K562 cells, growth inhibitory activity was determined by the MTT assay. To test the regeneration potential, a colony formation assay was performed. Cell cycle analyses were examined by flow cytometry. Cell injury was evaluated by lactate dehydrogenase (LDH) leakage. Real-time PCR was applied to assess the expression of IL6, TNF-α, STAT3, BAD, CASP3, TP53, and Bcl-2 genes. Caspase-3 activity was determined by a colorimetric assay. Antioxidant activity was measured using a diphenylpicrylhydrazyl (DPPH) assay. After 48 h of treatment, ATX (IC50 = 30µM) and CRC (IC50 = 190µM) significantly inhibited cell proliferation and colony formation ability, induced G1 cell cycle arrest and cell injury, upregulated the expression of apoptosis-associated genes, and downregulated the expression of anti-apoptotic and inflammatory genes. The combination of IM with ATX and/or CRC synergistically reduced cell viability (combination index [CI] < 1).

Conclusion: Our data suggest that IM shows better therapeutic efficacy at lower doses when combined with ATX and/or CRC.

Keywords: Astaxanthin; Chronic myeloid leukemia; Crocin; Drug resistance; Imatinib; K562 cells.

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References

    1. Soverini S, De Benedittis C, Mancini M, Martinelli G (2016) Best practices in chronic Myeloid Leukemia monitoring and management. Oncologist 21:626–633 - DOI - PubMed - PMC
    1. Cai H, Li L, Jiang J, Zhao C, Yang C (2019) Costunolide enhances sensitivity of K562/ADR chronic Myeloid Leukemia cells to doxorubicin through PI3K/Akt pathway. Phytother Res 33:1683–1688. https://doi.org/10.1002/ptr.6355 - DOI - PubMed
    1. Zhao M, Yang C, Chai S, Yuan Y, Zhang J, Cao P, Wang Y, Xiao X, Wu K, Yan H, Liu J, Sun S (2021) Curcumol and FTY720 synergistically induce apoptosis and differentiation in chronic myelomonocytic Leukemia via multiple signaling pathways. Phytother Res 35:2157–2170. https://doi.org/10.1002/ptr.6968 - DOI - PubMed
    1. Kang Y, Hodges A, Ong E, Roberts W, Piermarocchi C, Paternostro G (2014) Identification of drug combinations containing imatinib for treatment of BCR-ABL + leukemias. PLoS ONE 9:e102221 - DOI - PubMed - PMC
    1. Jabbour EJ, Hughes TP, Cortés JE, Kantarjian HM, Hochhaus A (2014) Potential mechanisms of Disease progression and management of advanced-phase chronic Myeloid Leukemia. Leuk Lymphoma 55:1451–1462 - DOI - PubMed

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