Asoudeh-Fard Abbas, Salehi Mitra, Ilghari Dariush, Parsaei Asghar, Heydarian Peyman, Piri Hossein
INSERM U1148, Laboratory for Vascular Translation Science (LVTS), Cardiovascular Bioengineering, University Sorbonne Paris North, Paris, France.
Research Center for Pharmaceutical Nanotechnology, Tabriz University of Medical Sciences, Tabriz, Iran.
Iran J Basic Med Sci. 2024;27(4):447-452. doi: 10.22038/IJBMS.2023.72825.15846.
It is worthwhile to note that, some probiotics such as and isolated from dairy products have significant therapeutic effects against cancer cells. Here, we evaluated anti-proliferation and the apoptotic effects of isolated Ab.RS22 from traditional dairy products on the HeLa cervical cancer cells
The viability of treated HeLa cells with supernatant of in 0.5, 0.75, 1, 1.5, and 2 ng/ml concentrations, and IC values were detected by tetrazolium bromide. The Ab.RS22-induced cell death by flow cytometry was confirmed through evaluation of the expression of , , , and genes by quantitative reverse transcription-polymerase chain reactions (qRT-PCR).
Most cytotoxicity effects of on HeLa cells were detected in 2 ng/ml at 24 hr (<0.01); also, the IC value was measured as 1.5 ng/ml. The findings of the flow cytometry assay showed that Ab.RS22 in 1.5 ng/ml concentration at 24 hr increased the percentage of both apoptosis and necrosis cells. Lactobacillus-induced cell death was verified through results of Real-time PCR; where expression of , , and genes was increased (<0.01), and also expression of gene (anti-apoptotic) was decreased (<0.05).
Our findings showed that Ab.RS22 could dose-dependently inhibit the proliferation of the HeLa cells. Its apoptotic effect was confirmed via modulating / gene expression and activation of the caspase-3 mediated apoptosis pathway. Therefore, Ab.RS22 can be considered a valuable anticancer candidate against cervical cancer progression in subsequent studies.
值得注意的是,一些从乳制品中分离出的益生菌,如[具体名称1]和[具体名称2],对癌细胞具有显著的治疗作用。在此,我们评估了从传统乳制品中分离出的Ab.RS22对人乳头瘤病毒18型(HPV-18)阳性的人宫颈癌HeLa细胞的抗增殖和凋亡作用。
用浓度为0.5、0.75、1、1.5和2 ng/ml的Ab.RS22上清液处理HeLa细胞,通过溴化四氮唑检测其活力,并测定半数抑制浓度(IC)值。通过定量逆转录聚合酶链反应(qRT-PCR)评估细胞凋亡相关基因(Bax、Bcl-2、Caspase-3和Caspase-9)的表达,以流式细胞术确认Ab.RS22诱导的细胞死亡。
在24小时时,2 ng/ml的Ab.RS22对HeLa细胞的细胞毒性作用最为显著(P<0.01);IC值为1.5 ng/ml。流式细胞术检测结果显示,24小时时,1.5 ng/ml浓度的Ab.RS22增加了凋亡细胞和坏死细胞的百分比。实时荧光定量PCR结果证实了嗜酸乳杆菌诱导的细胞死亡;其中,Bax、Caspase-3和Caspase-9基因的表达增加(P<0.01),而抗凋亡基因Bcl-2的表达降低(P<0.05)。
我们的研究结果表明,Ab.RS22可剂量依赖性地抑制HeLa细胞的增殖。通过调节Bax/Bcl-2基因表达和激活Caspase-3介导的凋亡途径,证实了其凋亡作用。因此,在后续研究中,Ab.RS22可被视为一种对抗宫颈癌进展的有价值的抗癌候选物。