膀胱癌植物适应基因细胞毒性药物组合物开发的计算机模拟可能性

IF 0.6 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
N. S. Ionov, M. A. Baryshnikova, E. V. Bocharov, P. V. Pogodin, A. A. Lagunin, D. A. Filimonov, R. V. Karpova, V. S. Kosorukov, I. S. Stilidi, V. B. Matveev, O. A. Bocharova, V. V. Poroikov
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引用次数: 2

摘要

利用PASS计算机程序对几种药用植物次生代谢产物的生物活性谱进行预测,并对预测结果进行体外验证,确定了药物组合物植物适应基因(phytotoladaptogene, PLA)开发的优先方向。聚乳酸是一种结构多样的小有机化合物复合物,包括植物适应基因的生物活性物质(人参皂苷,红景天等),根据先前开发的药物组合物编译。研究了药物组合物的两种变体-主要(22个化合物)和次要(13个化合物)。在主要版本PLA的1945个药理作用和机制中,有1400个活性概率超过非活性概率。预测活性范围广主要是由于化合物之间的结构相似性较低。一项计算机预测表明,少量和大量聚乳酸组合物具有抗膀胱癌、胃癌、结肠癌、卵巢癌和宫颈癌的可能性。研究发现,三种机制的活性预测概率值最高:凋亡激动剂、Caspase 3刺激剂和转录因子NF κ B抑制剂。根据PharmaExpert项目,它们与膀胱癌的抗肿瘤作用有关。在体外对人膀胱癌细胞株RT-112进行了实验验证。作为MTT测试的结果,PLA主要变型的细胞毒性被发现比次要变型高。体外实验采用膜联蛋白V和碘化丙啶双染色和检测细胞活性caspase 3两种方法,也证实了膀胱癌细胞凋亡的机制。所得数据与预测结果一致,表明了聚乳酸的主要成分优势。植物适应基因可成为开发具有抗肿瘤活性的膀胱癌药物的基础。通过PASS预测其他癌症的抗肿瘤活性可能是进一步研究的主题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possibilities of in Silico Estimations for the Development of the Pharmaceutical Composition Phytoladaptogene Cytotoxic for Bladder Cancer Cells

The priority direction of the pharmaceutical composition Phytoladaptogene (PLA) development based on the prediction of biological activity spectra for several secondary metabolites of medicinal plants using the PASS computer program and validation in vitro of the prediction result was determined. PLA is a complex of structurally diverse small organic compounds including biologically active substances of phytoadaptogenes (ginsenosides from Panax ginseng, rhodionin from Rhodiola rosea and others) compiled considering previously developed pharmaceutical compositions. Two variants of the pharmaceutical composition were studied—major (22 compounds) and minor (13 compounds) ones. The probability of activity exceeds the probability of inactivity for 1400 out of 1945 pharmacological effects and mechanisms predicted by PASS for the major version of PLA. The wide range of predicted activities is mainly due to the compounds' low structural similarity to each other. An in silico prediction indicates the possibilities of antitumor properties against bladder, stomach, colon, ovarian and cervical cancers both for minor and major PLA compositions. It was found that the highest probability values of activity are predicted for three mechanisms: Apoptosis agonist, Caspase 3 stimulant, and Transcription factor NF kappa B inhibitor. According to the PharmaExpert program, they are associated with the antitumor effect against bladder cancer. Experimental validation was performed in vitro on the human bladder cancer cell line RT-112. As a result of the MTT test the cytotoxicity of the PLA major variant was found to be higher than that of the minor one. In the in vitro experiments using two methods—double staining with annexin V and propidium iodide as well as detection of active caspase 3 in cells—the death of bladder cancer cells by the apoptosis mechanism was also confirmed. The data obtained correspond to the results of the prediction and indicate the major PLA composition advantages. Phytoladaptogene can become the basis for the development of a drug with antitumor activity against bladder cancer. Antitumor activity predicted by PASS for other cancers may be the subject of further studies.

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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
31
期刊介绍: Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry   covers all major aspects of biomedical chemistry and related areas, including proteomics and molecular biology of (patho)physiological processes, biochemistry, neurochemistry, immunochemistry and clinical chemistry, bioinformatics, gene therapy, drug design and delivery, biochemical pharmacology, introduction and advertisement of new (biochemical) methods into experimental and clinical medicine. The journal also publishes review articles. All issues of the journal usually contain solicited reviews.
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