Dehdashti Maryam, Abbasy Zahra, Zaferani Arani Hamid, Adin Atashi Hesam, Salimi-Tabatabaee Seyed Alireza, Ghasemi Afsaneh, Fereidouni Zhila, Zare Marzouni Hadi, Zakeri Habib, Mirmalek Seyed Abbas
Young Researchers and Elite Club, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Faculty of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Galen Med J. 2023 Jun 21;12:e3050. doi: 10.31661/gmj.v12i.3050. eCollection 2023.
Breast cancer (BC) is the major cause of cancer-related death in women. Some studies have indicated the cytotoxic effects of vanadyl oxide sulfate (VOSO4). This study aimed to evaluate the anti-cancer effect of VOSO4 in the treatment of MCF-7 cell lines.
The MCF-7 cell line was treated with different concentrations of VOSO4 for 24 and 48 hours. Cell death was measured using the MTT assay. The cell apoptosis rate was measured using Annexin V/Propidium Iodide assay through flow cytometry. Also, the expression levels of p53, P21, Caspase8, superoxide dismutase type 1 (SOD1), Sod2, and Bcl2 mRNAs were assessed, and Western blotting was performed for Sod1 protein.
The results showed that the half-maximal inhibitory concentration (IC50) for VOSO4 was 25 and 20 μg/ml for 24 and 48 hours, respectively. Indeed, VOSO4 has dose-dependent cytotoxic effects on the MCF-7. Also, after exposure to VOSO4 for 24 hours, cell apoptosis reached 52% compared with untreated cells. Moreover, after 24 hours of exposure to VOSO4 with IC50 concentration, the expression of p53, P21, Caspase8, Sod1, and Sod2 mRNAs increased (P0.05), and the expression of Bcl2 mRNA was decreased (P0.05). Also, the Western blotting revealed Sod1 protein level markedly increased following exposure to VOSO4 (P0.05).
Our results demonstrated that VOSO4 has an apoptotic and cytotoxic effect on BC cells. Therefore, it could be considered a complementary agent for the medical treatment of patients with BC.
乳腺癌(BC)是女性癌症相关死亡的主要原因。一些研究表明硫酸氧钒(VOSO4)具有细胞毒性作用。本研究旨在评估VOSO4对MCF-7细胞系的抗癌作用。
用不同浓度的VOSO4处理MCF-7细胞系24小时和48小时。使用MTT法检测细胞死亡情况。通过流式细胞术使用膜联蛋白V/碘化丙啶法检测细胞凋亡率。此外,评估p53、P21、Caspase8、超氧化物歧化酶1(SOD1)、Sod2和Bcl2 mRNA的表达水平,并对Sod1蛋白进行蛋白质印迹分析。
结果显示,VOSO4在24小时和48小时时的半数最大抑制浓度(IC50)分别为25μg/ml和20μg/ml。事实上,VOSO4对MCF-7具有剂量依赖性细胞毒性作用。此外,在暴露于VOSO4 24小时后,与未处理的细胞相比,细胞凋亡率达到52%。而且,在暴露于IC50浓度的VOSO4 24小时后,p53、P21、Caspase8、Sod1和Sod2 mRNA的表达增加(P<0.05),而Bcl2 mRNA的表达降低(P<0.05)。蛋白质印迹分析还显示,暴露于VOSO4后Sod1蛋白水平显著增加(P<0.05)。
我们的结果表明,VOSO4对BC细胞具有凋亡和细胞毒性作用。因此,它可被视为乳腺癌患者医学治疗的一种辅助药物。