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Background: Methylprednisolone (MP) is a pharmaceutical agent employed in the management of Leukemia, which is a systemic malignancy that arises from abnormalities in the hematological system. Numerous investigations in the field of cancer research have directed their attention towards propolis, a natural substance with significant potential as a treatment-supportive agent. Its utilization aims to mitigate the potential adverse effects associated with chemotherapy medications. The objective of this study was to examine the impact of olive oil-based propolis (OEP) and caffeic acid phenethyl ester (CAPE) on the treatment of acute myeloid leukemia, as well as to determine if they exhibit a synergistic effect when combined with the therapeutic support product methylprednisolone.
Methods And Results: The proliferation of HL-60 cells was quantified using the WST-8 kit. The PI Staining technique was employed to do cell cycle analysis of DNA in cells subjected to OEP, CAPE, and MP, with subsequent measurement by flow cytometry. The apoptotic status of cells was determined by analyzing them using flow cytometry after staining with the Annexin V-APC kit. The quantification of apoptotic gene expression levels was conducted in HL-60 cells. In HL-60 cells, the IC dosages of CAPE and MP were determined to be 1 × 10 M and 5 × 10 M, respectively. The HL-60 cells were subjected to apoptosis and halted in the G/G and G/M phases of the cell cycle after being treated with MP, CAPE, and OEP.
Conclusions: Propolis and its constituents have the potential to serve as effective adjunctive therapies in chemotherapy.
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http://dx.doi.org/10.1007/s11033-024-09493-7 | DOI Listing |
J Ayurveda Integr Med
September 2025
Kode Lab, Tumor Immunology & Immunotherapy (TII) Group; Advanced Centre for Treatment, Research & Education in Cancer (ACTREC), Tata Memorial Centre, Kharghar, Navi Mumbai, 410210, India; Anti-Cancer Drug Screening Facility (ACDSF), Advanced Centre for Treatment, Research and Education in Cancer (AC
Background: S. guineense DC. var.
View Article and Find Full Text PDFBiochem Biophys Rep
September 2025
Departamento de Inmunología, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Apdo. Postal 70228, Ciudad Universitaria, Ciudad de México, 04510, Mexico.
The promyelocytic HL-60 cell line can be differentiated toward neutrophil-like cells and has been historically used as a surrogate to study human neutrophil biology . Multiple differentiation protocols have been reported to generate neutrophil-like HL-60 cells, with limited consideration of how methodological variations might influence cell identity and functions. Here, we conducted a systematic search of the PubMed database, to investigate the current heterogeneity in published protocols used to differentiate HL-60 towards neutrophil-like cells.
View Article and Find Full Text PDFHematology
December 2025
Department of Hematology, The First Affiliated Hospital of Guangxi Medical University, Nanning, People's Republic of China.
Objectives: Lactylation- and liquid-liquid phase separation-related differentially expressed genes (LLRDEGs) have been implicated in cancer. However, their role in acute myeloid leukemia (AML) remains largely unexplored.
Methods: LLRDEGs associated with AML prognosis were identified using Cox regression and LASSO analyzes.
J Vis Exp
August 2025
Department of Biological Chemistry, Showa Medical University Graduate School of Pharmacy.
Neutrophil extracellular traps (NETs) have emerged as causative factors in various non-infectious diseases and have been implicated in cardiovascular disorders such as atherosclerosis and thrombosis. NET formation is observed in the vascular wall, and there is compelling evidence that plasma markers of NET formation increase with disease severity. Neutrophil-derived NET components, including myeloperoxidases and proteases, affect plasma lipoproteins and vascular homeostasis.
View Article and Find Full Text PDFCancer Genomics Proteomics
August 2025
Department of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan, R.O.C.;
Background/aim: Cytarabine is the main chemotherapy agent used to treat acute myeloid leukemia (AML), but drug resistance remains a major challenge. Imbalances in cytokine secretion are known to play a role in the survival and proliferation of AML blast cells. While numerous studies have investigated cytokine secretion in AML, the precise role of cytokines in the pathogenesis of AML remains unclear.
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