Protective Role of Royal Jelly on the Growth of the MCF-10A Cell LineTreated with Cisplatin

被引:0
作者
Abedikanzagh, Fatemeh [1 ]
Fard, Zahra Tahmasebi [2 ]
Hasanzad, Mandana [1 ]
机构
[1] Islamic Azad Univ, Dept Med Genom Res Ctr, Tehran Med Sci, Tehran, Iran
[2] Islamic Azad Univ, Dept Biol, Roudehen Branch, Roudehen, Iran
关键词
Cisplatin; Royal Jelly; MCF-10A Cell Line; MTT Assay; BREAST-CANCER;
D O I
10.5812/ijcm-160408
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Royal jelly (RJ) possesses numerous beneficial properties. When used in conjunction with pharmacological agents, it may enhance the inhibition of tumor growth and help manage the side effects induced by drugs. Objectives: The present study aimed to examine the simultaneous effects of RJ and cisplatin on the growth rate of normal breast cells. Methods: The MCF-10A cell line (CRL-10317) was obtained from the Avicenna Research Institute cell bank in Iran. Following cell culture (at 37 degrees C in an incubator with 5% Co-2), the cells were treated with serial concentrations of cisplatin and RJ, ranging from 0 to 5 - 10 - 20 - 30 - 40 - 50 - 75 - 100 - 250 mu g/mL and 500 mu g/mL, respectively, for durations of 24, 48, and 72 hours. Cell viability was assessed using the MTT assay, with one-way ANOVA and post-hoc tests (LSD and Tukey) for statistical analysis. The study protocol was approved by the Ethics Committee of Islamic Azad University, Tehran Medical Branch (IR.IAU.PS.REC.1401.138). Results: Cisplatin alone reduced MCF-10A cell growth across all time points (P < 0.0001). Royal jelly at concentrations above 40 mu g/mL increased cell growth after 48 hours (P = 0.00217) and 72 hours (P < 0.0001). Combined treatment initially decreased growth (P < 0.0001), but higher concentrations stabilized cell viability after 72 hours, suggesting a protective effect. Conclusions: Royal jelly demonstrates a protective role against cisplatin-induced toxicity in normal breast cells, potentially preserving healthy tissue during chemotherapy. These findings, while promising for adjunctive therapies, require further validation in diverse cell lines and clinical settings to confirm generalizability.
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