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首页> 外文期刊>International Journal of Preventive Medicine >Imminent Angiotensin-converting Enzyme Inhibitor from Microbial Source for Cancer Therapy
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Imminent Angiotensin-converting Enzyme Inhibitor from Microbial Source for Cancer Therapy

机译:来自微生物来源的即将到来的血管紧张素转换酶抑制剂用于癌症治疗

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Background: Drugs targeting Angiotensin I-converting enzyme (ACE) have been used broadly in cancer chemotherapy. The recent past coupled with our results demonstrates the effective use of ACE inhibitors (ACEi) as anticancer agents, and they are potentially relevant in deriving new inhibitors. Methods: Bacterial strains were isolated from cow milk collected in Coimbatore, Tamil Nadu, India and plated on nutrient agar medium. The identity of the strain was ascertained by 16s rRNA gene sequencing method and was submitted to the NCBI GenBank nucleotide database. Various substrates were screened for ACEi production by the fermentation with the isolated strain. ACEi was purified by sequential steps of ethanol precipitation, ion exchange column chromatography and gel filtration column chromatography. The apparent molecular mass was determined by SDS-PAGE. The anticancer property was analyzed by studying the cytotoxicity effects of ACEi using Breast cancer MCF-7 cell lines Results: The isolate coded as BUCTL09 was selected and identified as Micrococcus luteus. Among the seven substrates, only beef extract fermented broth showed an inhibition of 79% and was reported as the best substrate. The peptide was purified and molecular mass was determined. The IC50 value of peptide was found to be 59.5 μg/ml. The purified peptide has demonstrated to induce apoptosis of cancer cell. Conclusions: The results of this study revealed that Peptide has been determined as an active compound that inhibited the activity of ACE. These properties indicate the possibilities of the use of purified protein as a potent anticancer agent.
机译:背景:靶向血管紧张素I转换酶(ACE)的药物已广泛用于癌症化疗。最近的研究结果与我们的研究结果一起证明了ACE抑制剂(ACEi)作为抗癌药的有效使用,它们在开发新抑制剂方面可能具有重要意义。方法:从印度泰米尔纳德邦哥印拜陀收集的牛奶中分离出细菌菌株,并将其铺在营养琼脂培养基上。通过16s rRNA基因测序方法确定菌株的身份,并将其提交至NCBI GenBank核苷酸数据库。通过用分离的菌株发酵来筛选各种底物的ACEi产生。通过乙醇沉淀,离子交换柱色谱和凝胶过滤柱色谱的连续步骤纯化ACEi。通过SDS-PAGE确定表观分子量。通过使用乳腺癌MCF-7细胞系研究ACEi的细胞毒性作用来分析其抗癌性。结果:选择编码为BUCTL09的分离株,并将其鉴定为黄斑微球菌。在这七种底物中,只有牛肉提取物发酵液显示出79%的抑制作用,据报道是最好的底物。纯化肽并测定分子量。发现肽的IC50值为59.5μg/ ml。纯化的肽已证明可诱导癌细胞凋亡。结论:这项研究的结果表明,肽已被确定为抑制ACE活性的活性化合物。这些性质表明使用纯化的蛋白质作为有效的抗癌剂的可能性。

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