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Cytotoxic and Apoptotic Effects of Vanadyl Sulfate on MCF-7 Breast Cancer Cell Line
被引:0
|作者:
Dehdashti, Maryam
[1
]
Abbasy, Zahra
[2
]
Arani, Hamid Zaferani
[3
]
Atashi, Hesam Adin
[1
]
Salimi-Tabatabaee, Seyed Alireza
[4
]
Ghasemi, Afsaneh
[5
]
Fereidouni, Zhila
[6
]
Marzouni, Hadi Zare
[7
]
Zakeri, Habib
[8
]
Mirmalek, Seyed Abbas
[9
,10
]
机构:
[1] Islamic Azad Univ, Young Researchers & Elite Club, Tehran Med Sci, Tehran, Iran
[2] Kashan Univ Med Sci, Fac Med, Kashan, Iran
[3] Univ Tehran Med Sci, Shariati Hosp, Dept Surg, Tehran, Iran
[4] Kashan Univ Med Sci, Dept Surg, Kashan, Iran
[5] Fasa Univ Med Sci, Sch Hlth, Dept Publ Hlth, Fasa, Iran
[6] Fasa Univ Med Sci, Sch Nursing, Dept Nursing, Fasa, Iran
[7] Birjand Univ Med Sci, Qaen Sch Nursing & Midwifery, Birjand, Iran
[8] Shiraz Univ Med Sci, Res Ctr Neuromodulat & Pain, NAB Pain Clin, Shiraz, Iran
[9] Islamic Azad Univ, Dept Surg, Tehran Med Sci, Tehran, Iran
[10] Islamic Azad Univ, Fac Med, Dept Surg, Tehran Med Sci, Tehran, Iran
来源:
GALEN MEDICAL JOURNAL
|
2023年
/
12卷
关键词:
Vanadyl Sulfate;
Breast Cancer;
Anti-cancer;
MCF-7;
Apoptosis;
Anti-oxidative;
MEDIATED APOPTOSIS;
MORPHOLOGY;
PENTOXIDE;
GROWTH;
DAMAGE;
VOSO4;
D O I:
10.31661/gmj.v12i0.3050
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Background: 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. Materials and Methods: 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 apop-tosis 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. Results: The results showed that the half-maximal inhibitory concentration (IC50) for VOSO4 was 25 and 20 mu g/ml for 24 and 48 hours, respectively. Indeed, VOSO4 has dose-dependent cyto-toxic 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 (P<0.05), and the expression of Bcl2 mRNA was decreased (P<0.05). Also, the Western blotting revealed Sod1 protein level markedly increased following exposure to VOSO4 (P<0.05). Conclusion: Our results demonstrated that VOSO4 has an apoptotic and cytotoxic effect on BC cells. There-fore, it could be considered a complementary agent for the medical treatment of patients with BC.
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