微藻衍生生物活性化合物作为B-Raf v600e驱动的黑色素瘤新抑制剂的计算模拟

Q2 Pharmacology, Toxicology and Pharmaceutics
F. Prasetiya, Wanda Destiarani, Irene Retno Cahya Prihastaningtyas, Mochamad Untung Kurnia Agung, Muhammad Yusuf
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引用次数: 0

摘要

黑色素瘤是最具侵袭性的癌症之一,在过去的50年里发病率急剧上升。由于低反应率和10年生存率,晚期黑色素瘤的治疗仍然是一个挑战。因此,需要努力研发药物来对抗这种癌症。迄今为止,大数据和3D技术的发展使研究人员更容易了解在黑色素瘤癌症中作为受体发挥重要作用的蛋白质或酶的结构,并将其用作诊断和治疗的特定靶点,例如B-Raf V600E。本研究考察了微藻中活性化合物开发黑色素瘤抗癌药物的潜力。该数据库是利用1970 - 2020年MarinLit和相关出版物的数据挖掘构建的。利用分子对接、虚拟筛选和分子动力学模拟等计算机方法寻找最有潜力的候选分子。共有25个化合物通过了虚拟筛选阶段。与天然配体和商业药物相比,结合自由能排名前三的化合物是胆甾醇-5,7-二烯-3 - β -醇、24-氧胆固醇醋酸酯、胆甾醇,以及另外两种化合物藻蓝蛋白和藻蓝胆素,这两种化合物也被选中,因为它们在世界上最常见的培养微藻节肢螺旋藻中大量生产。此外,还进行了ADME分析和毒性试验。分子动力学模拟表明,藻蓝蛋白的自由结合能在−65 ~−80 kcal/mol之间,是黑色素瘤抗癌药物的最佳候选物质。均方根偏差、均方根波动和距离参数数据也支持这一结果。这项研究可能会加速黑色素瘤癌症治疗化合物的分子研究,从而使其能够继续开发有益于人类健康的药物产品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Computational simulations of microalgae-derived bioactive compounds as a novel inhibitor against B-Raf V600E-driven melanoma
Melanoma is one of the most aggressive types of cancer, which has shown a tremendous surge in the last 50 years. Therapy for advanced-type melanoma is still a challenge because of the low response rate and 10-year survival. Therefore, drug discovery efforts need to be made to fight this cancer. To date, the development of big data and 3D has made it easier for researchers to understand the structure of proteins or enzymes that play an important role as receptors in melanoma cancer to be used as specific targets for diagnosis and therapy, for instance, the B-Raf V600E. This study examined the potential of active compounds from microalgae for developing melanoma anticancer drugs. The database was constructed using data mining from MarinLit and the related publications from 1970 to 2020. In silico methods such as molecular docking, virtual screening, and molecular dynamic simulations were used to find the most potential candidates. A total of 25 compounds passed the virtual screening stage. The top three compounds based on the binding free energy compared to a natural ligand and commercial drug are cholesta-5,7-dien-3beta-ol, 24-oxocholesterol acetate, lathosterol, and two additional compounds, phycocyanin and phycocyanobilin, were also selected due to their massive production from the most commonly cultured microalgae worldwide, Arthrospira sp. (previously known as Spirulina sp.). Furthermore, ADME analysis and toxicity tests were also carried out. Molecular dynamics simulation showed that phycocyanin was the best potential candidate for melanoma anticancer drugs, with free binding energies ranging from −65 to −80 kcal/mol. This result was also supported by root mean square deviation, root mean square fluctuation, and distance parameter data. This study may accelerate molecular research in producing therapeutic compounds for melanoma cancer, thus allowing it to continue developing pharmaceutical products that benefit human health.
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来源期刊
journal of applied pharmaceutical science
journal of applied pharmaceutical science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
2.20
自引率
0.00%
发文量
224
期刊介绍: Journal of Applied Pharmaceutical Science (JAPS) is a monthly, international, open access, journal dedicated to various disciplines of pharmaceutical and allied sciences. JAPS publishes manuscripts (Original research and review articles Mini-reviews, Short communication) on original work, either experimental or theoretical in the following areas; Pharmaceutics & Biopharmaceutics Novel & Targeted Drug Delivery Nanotechnology & Nanomedicine Pharmaceutical Chemistry Pharmacognosy & Ethnobotany Phytochemistry Pharmacology & Toxicology Pharmaceutical Biotechnology & Microbiology Pharmacy practice & Hospital Pharmacy Pharmacogenomics Pharmacovigilance Natural Product Research Drug Regulatory Affairs Case Study & Full clinical trials Biomaterials & Bioactive polymers Analytical Chemistry Physical Pharmacy.
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