Vitamin D3, arsenic trioxide, or combination therapy for acute promyelocytic leukemia
Arsenic trioxide (ATO) has been a highly promising chemotherapeutic drug for treating APL patients in the last decades. Owing to its complications, researchers are enthusiastic about applying compounds with fewer side effects, especially in a combined modality. Therefore, due to the anti-cancer prop...
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Published in | Gene reports Vol. 27; p. 101576 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Inc
01.06.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Arsenic trioxide (ATO) has been a highly promising chemotherapeutic drug for treating APL patients in the last decades. Owing to its complications, researchers are enthusiastic about applying compounds with fewer side effects, especially in a combined modality. Therefore, due to the anti-cancer properties of VitD3, our investigation was aimed to highlight the Vit-D3/ATO combination effects on the NB4 leukemic cells.
The APL cell line (NB4) was cultured with various VitD3, ATO, and Vit-D3/ATO concentrations. Afterward, the cell viability was evaluated via MTT and trypan blue assays. In addition, the apoptosis and Gene expression were assessed using Flow cytometry and qRT-PCR, respectively.
Our findings revealed that Vit-D3 applied apoptotic and growth inhibitory effects in a dose and time-dependent manner. Moreover, Vit-D3/ATO combination augmented the effects of ATO on regulated cell death via a remarkable elevation in the BAX/BCL-2 ratio in comparison with single treatments.
Given the synergistic effects of the Vit-D3/ATO combination, our study suggests a promising therapeutic strategy for APL treatment.
•Vit-D3 and ATO Combination synergistically inhibit the NB4 cells' viability.•Vit-D3 and ATO Combination synergistically decreases NB4 cells' metabolic activity.•Vit-D3 and ATO Combination synergistically increase the apoptosis in NB4 cells.•Vit-D3 and ATO Combination synergistically increased the BAX/BCL-2 genes expression. |
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ISSN: | 2452-0144 2452-0144 |
DOI: | 10.1016/j.genrep.2022.101576 |