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联合使用[具体方法1]、[具体方法2]和[具体方法3]分析评估来自蓝藻菌MGL001的一种生物活性化合物的抗癌潜力。

The Combined Use of , and Analyses to Assess Anti-cancerous Potential of a Bioactive Compound from Cyanobacterium sp. MGL001.

作者信息

Verma Ekta, Maurya Shashank K, Mishra Rajnikant, Mishra Arun K

机构信息

Laboratory of Microbial Genetics, Department of Botany, Banaras Hindu University, Varanasi, India.

Biochemistry and Molecular Biology Laboratory, Department of Zoology, Banaras Hindu University, Varanasi, India.

出版信息

Front Pharmacol. 2017 Nov 27;8:873. doi: 10.3389/fphar.2017.00873. eCollection 2017.

Abstract

Escalating incidences of cancer, especially in developed and developing countries, demand evaluation of potential unexplored natural drug resources. Here, anticancer potential of 9-Ethyliminomethyl-12-(morpholin-4-ylmethoxy)-5,8,13,16-tetraaza -hexacene-2,3-dicarboxylic acid (EMTAHDCA) isolated from fresh water cyanobacterium sp. MGL001 was screened through , and studies. For analysis, EMTAHDCA was selected as ligand and 11 cancer related proteins (Protein Data Bank ID: 1BIX, 1NOW, 1TE6, 2RCW, 2UVL, 2VCJ, 3CRY, 3HQU, 3NMQ, 5P21, and 4B7P) which are common targets of various anticancer drugs were selected as receptors. The results obtained from analysis showed that EMTAHDCA has strong binding affinity for all the 11 target protein receptors. The ability of EMTAHDCA to bind active sites of cancer protein targets indicated that it is functionally similar to commercially available anticancer drugs. For assessing cellular metabolic activities, studies were performed by using calorimetric assay . 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide (MTT). Results showed that EMTAHDCA induced significant cytotoxic response against Dalton's lymphoma ascites (DLA) cells in a dose and time dependent manner with an inhibitory concentration (IC) value of 372.4 ng/mL after 24 h of incubation. However, in case of normal bone marrow cells, the EMTAHDCA did not induce cytotoxicity as the IC value was not obtained even with higher dose of 1,000 ng/mL EMTAHDCA. Further, studies revealed that the median life span/survival days of tumor bearing mice treated with EMTAHDCA increased significantly with a fold change of ~1.9 and 1.81 corresponding to doses of 5 and 10 mg/kg body weight (B.W.) of EMTAHDCA respectively, as compared to the DL group. Our results suggest that 5 mg/kg B.W. is effective since the dose of 10 mg/kg B.W. did not show any significant difference as compared to 5 mg/kg B.W. Taken together, our findings based on , and analyses suggest that EMTAHDCA has potential anticancer effects, and thus, can be considered for cancer treatment.

摘要

癌症发病率不断上升,尤其是在发达国家和发展中国家,这就需要对潜在的未开发天然药物资源进行评估。在此,对从淡水蓝藻MGL001中分离出的9-乙基亚氨基甲基-12-(吗啉-4-基甲氧基)-5,8,13,16-四氮杂并六苯-2,3-二羧酸(EMTAHDCA)的抗癌潜力进行了[此处原文缺失具体实验方法,无法准确翻译]和[此处原文缺失具体实验方法,无法准确翻译]研究。为了进行[此处原文缺失具体实验方法,无法准确翻译]分析,选择EMTAHDCA作为配体,并选择11种与癌症相关的蛋白质(蛋白质数据库ID:1BIX、1NOW、1TE6、2RCW、2UVL、2VCJ、3CRY、3HQU、3NMQ、5P21和4B7P)作为受体,这些蛋白质是各种抗癌药物的常见靶点。[此处原文缺失具体实验方法,无法准确翻译]分析得到的结果表明,EMTAHDCA对所有11种靶蛋白受体都具有很强的结合亲和力。EMTAHDCA与癌症蛋白靶点活性位点结合的能力表明,它在功能上与市售抗癌药物相似。为了评估细胞代谢活性,使用比色法[此处原文缺失具体实验方法,无法准确翻译]进行了[此处原文缺失具体实验方法,无法准确翻译]研究。采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)。结果表明,EMTAHDCA对道尔顿淋巴瘤腹水(DLA)细胞具有显著的细胞毒性反应,呈剂量和时间依赖性,孵育24小时后抑制浓度(IC)值为372.4 ng/mL。然而,对于正常骨髓细胞,EMTAHDCA未诱导细胞毒性,因为即使使用高达1000 ng/mL的更高剂量EMTAHDCA也未获得IC值。此外,[此处原文缺失具体实验方法,无法准确翻译]研究表明,与DL组相比,用EMTAHDCA治疗的荷瘤小鼠的中位寿命/存活天数显著增加分别对应于EMTAHDCA 5和10 mg/kg体重(B.W.)剂量的倍数变化约为1.9和1.81。我们的结果表明,5 mg/kg B.W.是有效的,因为与5 mg/kg B.W.相比,10 mg/kg B.W.的剂量没有显示出任何显著差异。综上所述,我们基于[此处原文缺失具体实验方法,无法准确翻译]、[此处原文缺失具体实验方法,无法准确翻译]和[此处原文缺失具体实验方法,无法准确翻译]分析的结果表明,EMTAHDCA具有潜在的抗癌作用,因此可考虑用于癌症治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7569/5711831/635aa3c3b046/fphar-08-00873-g0001.jpg

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