Maali Amirhosein, Ferdosi-Shahandashti Elaheh, Sadeghi Farzin, Aali Ehsan
Infectious Diseases and Tropical Medicine Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Int J Hematol Oncol Stem Cell Res. 2020 Oct 1;14(4):257-264. doi: 10.18502/ijhoscr.v14i4.4482.
Adult T-cell leukemia/lymphoma (ATLL) is a poor prognostic Hematopoietic malignancy with various therapeutic challenges, which had been classified as non-Hodgkin lymphoma. The Drug switching, as a novel, innovative and promising approach, is an opportunity to overcoming on therapeutic challenges of hard-treating disease, . ATLL. Our aim is evaluating the antiproliferative and apoptotic effect of Mebendazole (MBZ) on ATLL cancer cells in conditions. We used Jurkat cell-line as ATLL cancer cells. After treatment of MBZ in different concentrations on jurkat cells, the cell viabilities were determined by MTT assay. After IC value determination, the 24-, 48- and 72-h treatments had been performed in IC concentration and control to evaluating the quantitative apoptosis rate by Annexin/PI Flowcytometry and qualitative apoptosis by DAPI Nuclear staining. Also, Glucose spectrophotometry were performed to evaluate the reduced amount of glucose uptake through MBZ treatment. MBZ inhibits proliferation of jurkat cells and IC value had been estimated 10 μM (). According to the flowcytometric results, increasing in drug concentration is associated with decrease cell viability and the percentage of full-apoptosis. However, it inversely correlates with percentage of early-apoptosis rate. Also, the microscopic captures of DAPI Nuclear staining confirms the flowcytometry results in qualitative manner. In addition, it was found that inhibition of glucose uptake was inversely correlated with increased MBZ concentration (). MBZ potentially inhibits the proliferation of ATLL cancer cells in condition. MBZ inhibits the growth of Jurkat cells by inducing apoptosis. Also, we suggest that indirectly inhibition of Glucose transporting occurs by MBZ, which could induce apoptosis in cancer cells.
成人T细胞白血病/淋巴瘤(ATLL)是一种预后较差的造血系统恶性肿瘤,面临各种治疗挑战,曾被归类为非霍奇金淋巴瘤。药物转换作为一种新颖、创新且有前景的方法,是克服ATLL等难治性疾病治疗挑战的一个契机。我们的目的是评估甲苯咪唑(MBZ)在体外条件下对ATLL癌细胞的抗增殖和凋亡作用。我们使用Jurkat细胞系作为ATLL癌细胞。用不同浓度的MBZ处理Jurkat细胞后,通过MTT法测定细胞活力。在确定IC值后,在IC浓度和对照条件下进行24小时、48小时和72小时的处理,以通过Annexin/PI流式细胞术评估定量凋亡率,并通过DAPI核染色评估定性凋亡。此外,进行葡萄糖分光光度法以评估通过MBZ处理后葡萄糖摄取量的减少。MBZ抑制Jurkat细胞的增殖,估计IC值为10μM()。根据流式细胞术结果,药物浓度的增加与细胞活力降低和完全凋亡百分比降低相关。然而,它与早期凋亡率百分比呈负相关。此外,DAPI核染色的显微镜图像以定性方式证实了流式细胞术结果。此外,发现葡萄糖摄取的抑制与MBZ浓度增加呈负相关()。MBZ在体外条件下可能抑制ATLL癌细胞的增殖。MBZ通过诱导凋亡抑制Jurkat细胞的生长。此外,我们认为MBZ间接抑制葡萄糖转运,这可能诱导癌细胞凋亡。