Karimi Dermani Fatemeh, Saidijam Massoud, Najafi Rezvan, Moradkhani Shirin, Mohammadzaheri Zahra, Beiranvand Negar, Mohammadi Samane, Shabab Noushin, Kalvandi Ramazan, Zeraati Fatemeh
Research Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Medicinal Plants and Natural Products Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Avicenna J Phytomed. 2021 May-Jun;11(3):258-268.
Chemoprevention of cancer by application of natural phytochemical compounds has been used to prevent, delay or suppress cancer progression. a traditional Iranian medicinal herb, has biological properties including anticancer, anti-aging, immuno-stimulatory and antioxidant effects. In this study, anti-proliferative effects of hydroalcoholic extract of on prostate (PC3) and breast (MCF7) cancer cell lines were investigated.
In the current study, we investigated treatment of PC3 cells with different concentrations of (0, 100, 200, 300, 400, and 500 µg/ml) for 24 and 48 hr; also, MCF7 cells were treated with various concentrations (0-600 µg/ml) of for 48 and 72 hr and cell viability was assessed by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. mRNA expression of BCL2 Associated X (), B-cell lymphoma 2 (), Cysteine-aspartic proteases () and Phosphatase and tensin homolog () were analyzed by quantitative real-time PCR. Annexin V/PI staining and lactate dehydrogenase (LDH) cytotoxicity assay were used to detect apoptosis.
decreased PC3 and MCF7 cells viability in a dose- and time-dependent manner (p<0.01 to p<0.001). The gene expression of ratio, and increased in -treated cells compared to the control group. induced apoptosis (p<0.001) and LDH activity (p<0.01 to p<0.001).
Our findings suggest that extract is able to inhibit proliferation and induce apoptosis in PC3 and MCF7 cell lines. Therefore, extract exerts antitumor activity against cancer cells.
应用天然植物化学化合物进行癌症化学预防已被用于预防、延缓或抑制癌症进展。一种传统的伊朗药草,具有包括抗癌、抗衰老、免疫刺激和抗氧化作用在内的生物学特性。在本研究中,研究了该植物水醇提取物对前列腺(PC3)和乳腺(MCF7)癌细胞系的抗增殖作用。
在本研究中,我们用不同浓度(0、100、200、300、400和500μg/ml)的该植物处理PC3细胞24小时和48小时;此外,用不同浓度(0 - 600μg/ml)的该植物处理MCF7细胞48小时和72小时,并通过3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐(MTT)法评估细胞活力。通过定量实时PCR分析BCL2相关X蛋白(BAX)、B细胞淋巴瘤2(BCL2)、半胱天冬酶(CASPASE)和磷酸酶及张力蛋白同源物(PTEN)的mRNA表达。采用膜联蛋白V/碘化丙啶(Annexin V/PI)染色和乳酸脱氢酶(LDH)细胞毒性试验检测细胞凋亡。
该植物以剂量和时间依赖性方式降低PC3和MCF7细胞活力(p<0.01至p<0.001)。与对照组相比,该植物处理的细胞中BAX/BCL2比值、CASPASE和PTEN的基因表达增加。该植物诱导细胞凋亡(p<0.001)和LDH活性(p<0.01至p<0.001)。
我们的研究结果表明,该植物提取物能够抑制PC3和MCF7细胞系的增殖并诱导细胞凋亡。因此,该植物提取物对癌细胞具有抗肿瘤活性。