Cytotoxic Effects of the Ethanol Bane Skin Extract in Human Prostate Cancer Pc3 Cells.

Iranian journal of cancer prevention Pub Date : 2016-02-23 eCollection Date: 2016-04-01 DOI:10.17795/ijcp-4755
Maryam Amiri, Faranak Kazerouni, Saeed Namaki, Hassan Darbandi Tamijani, Hooman Rahimipour, Nasrin Boroumand, Siyamak Barghi, Nazanin Ebrahimi, Seyed Mohammad Gheibi Hayat
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引用次数: 6

Abstract

Background: It is extensively supposed that vegetarian diet could affect cancer progress and increase the influence of formal chemotherapy.

Objectives: The present study was designed to determine the effect of the ethanol Bane skin extract against chemo resistant prostate cancer PC3 cells.

Materials and methods: PC3 and L929 cells were cultivated and then incubated in the ethanol Bane skin extract with various concentrations of 0.78, 1.5, 3.13, 6.25, 12.5 mg/mL in 3 times 24, 48, 72 hours. Cytotoxic effect of the ethanol Bane skin extract on PC3 and L929 cells was examined by MTT assay after 24, 48, and 72 hours. Morphology of PC3 cells was evaluated by Gimsa staining.

Results: The ethanol Bane skin extract inhibited proliferation and caused cell death with IC50 values of 2.8 mg/mL on PC3 cells and the IC50 was 6.1 mg/mL on l929 cells. Morphological changes and apoptotic bodies were observed in PC3 cells faced with the ethanol Bane skin extract by staining with Gimsa.

Conclusions: The ethanol Bane skin extract could repress the growth of PC3 cell line. This inhibitory effect of the Bane extract depended on the dose and the time on PC3. The result of this study shows that the ethanol Bane skin extract includes photochemical and inhibitory function against proliferation and inducer of apoptosis in human prostate cancer PC3 cells and also has less cytotoxic effect on l929 than PC3 cells. The ethanol Bane skin extract might be a good candidate for the new herbal anticancer drug.

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Abstract Image

乙醇毒药皮肤提取物对人前列腺癌Pc3细胞的细胞毒性作用。
背景:人们普遍认为素食可以影响癌症的进展,并增加正规化疗的影响。目的:本研究旨在确定乙醇贝恩皮肤提取物对化疗耐药前列腺癌PC3细胞的作用。材料与方法:培养PC3和L929细胞,分别用浓度为0.78、1.5、3.13、6.25、12.5 mg/mL的乙醇提取物孵育24、48、72小时。24、48、72 h后,采用MTT法检测乙醇提取物对PC3、L929细胞的细胞毒作用。采用Gimsa染色法观察PC3细胞形态。结果:乙醇麻皮提取物对PC3细胞的IC50值为2.8 mg/mL,对2929细胞的IC50值为6.1 mg/mL,可抑制细胞增殖并导致细胞死亡。用Gimsa染色法观察到乙醇提取物对PC3细胞的形态学改变和凋亡小体的影响。结论:乙醇麻皮提取物可抑制PC3细胞株的生长。该提取物对PC3的抑制作用与剂量和时间有关。本研究结果表明,乙醇麻皮提取物对人前列腺癌PC3细胞具有光化学、抑制增殖和诱导凋亡的作用,对29细胞的细胞毒作用小于PC3细胞。乙醇提取物可能是一种新的草药抗癌药物的候选物。
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