Future medicine

  • 文章类型: Systematic Review
    背景:癌症是导致死亡的主要原因,癌细胞由于长期暴露于补充化疗治疗而产生耐药性的易感性被称为多药耐药癌细胞(MDRC),这是恶性肿瘤治疗的一个重要障碍。由于补充药物失去了效力,近年来,开发潜在的替代和新颖的治疗方法已被提升为重中之重。在这种情况下,来自植物和动物来源的生物活性蛋白凝集素显示出具有巨大治疗潜力的抗癌药物的宝贵来源。
    目的:本手稿的主要目的是启发基于证据的(从1986年到2022年)使用凝集素替代治疗方法的可能分子机制,而不是用于癌症治疗的补充药物。
    方法:已适当遵循PRISMA规则,并系统地综合了定性和定量数据。文章是基于临床和临床前报告发表的凝集素,研究了深入的细胞机制,逆转药物综合肿瘤学,作为纳米携带的靶向递送。1986年至2022年对文章进行了系统筛选,并根据电子数据库搜索进行了筛选,Medline(PubMed),谷歌学者,WebofScience,百科全书,Scopus,和ClinicalTrials.gov数据库。
    结果:搜索发现了来自38个不同国家的4,212种出版物,其中170篇参考文章被用于我们的分析,在16种联合疗法及其作用方式中,包括剂量和作用机制的27项临床试验研究。纳入了属于28个不同家庭的30种凝集素的报告。根据一些临床和临床前报告,对凝集素的逆转机制和针对MDRC的替代疗法进行了严格的筛选,凝集素可以抑制过表达的基因,如P-53,EGFR,还有P-GP,MRP,和ABC转运蛋白与药物的细胞内运输有关。因为,药物外排机制导致MDRC,在这种现象中,凝集素在逆转外排机制中起关键作用。很少有临床前报道提到,凝集素与补充药物结合显示出协同作用,并且作为纳米药物载体有助于递送到靶向部位。
    结论:我们已经讨论了使用凝集素的替代疗法,并深入了解了对抗MDRC癌症的逆转耐药机制,增强功效,减少毒性和不良事件,并确保有针对性的交付,并对其在癌症诊断和预后方面的应用进行了讨论。然而,在药物开发和临床试验中需要进一步的研究,这可能有助于阐述MDRC癌症的逆转机制和开启新的治疗模式.
    BACKGROUND: Cancer is characterized as the leading cause of death, and the susceptibility of cancer cells to develop resistance due to long-term exposure to complementary chemotherapeutic treatment is referred to as multidrug resistance cancer cells (MDRC), which is a significant obstacle in the treatment of malignancies. Since complementary medicine lost its effectiveness, the development of potential alternative and novel therapeutic approaches has been elevated to a top priority in recent years. In this context, a bioactive protein lectin from plant and animal sources exhibits an invaluable source of anticancer agents with vast therapeutic potential.
    OBJECTIVE: This manuscript\'s primary purpose is to enlighten the evidence-based (from 1986 to 2022) possible molecular mechanism of alternative treatment approaches using lectins over the complementary medicines used for cancer treatment.
    METHODS: The PRISMA rules have been followed properly and qualitative and quantitative data are synthesized systematically. Articles were identified based on Clinical and preclinical reports published on lectin that investigated the in-depth cellular mechanisms, of reverse drug integrative oncology, as a nano-carried targeted delivery. Articles were systematically screened from 1986 to 2022 and selected based on electronic database searches, Medline (PubMed), Google Scholar, Web of Science, Encyclopaedias, Scopus, and ClinicalTrials.gov database.
    RESULTS: The search turned up 4,212 publications from 38 different nations, of which 170 reference articles were used in our analysis, in 16 combination therapy and their mode of action, and 27 clinical trial studies including dosage and mechanism of action were included. Reports from the 30 lectins belonging to 28 different families have been included. The reversal mechanism of lectin and alternative therapy against MDRC is critically screened and according to a few clinical and preclinical reports, lectin can suppress the overexpressing genes like P-53, EGFR, and P-gp, MRP, and ABC transporter proteins associated with intracellular transportation of drugs. Since, the drug efflux mechanism leads to MDRC, in this phenomenon, lectin plays a key role in reversing the efflux mechanism. Few preclinical reports have mentioned that lectin shows synergism in combination with complementary medicine and as a nano drug carrier helps to deliver to the targeted site.
    CONCLUSIONS: We have discussed the alternative therapy using lectin and an in-depth insight into the reversal drug resistance mechanisms to combat MDRC cancer, enhance the efficacy, reduce toxicity and adverse events, and ensure targeted delivery, and their application in the field of cancer diagnosis and prognosis has been discussed. However, further investigation is necessary in drug development and clinical trials which could be helpful to elaborate the reversal mechanism and unlock newer treatment modalities in MDRC cancer.
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  • 文章类型: Journal Article
    背景:抗生素抗性细菌构成全球健康威胁。传统抗生素会失去效力,近年来,开发新型有效的抗菌药物已成为当务之急。在这个领域,植物代表了具有巨大治疗潜力的抗菌化合物的宝贵来源。
    目的:回顾植物抗菌药物的全部可能范围(植物化合物,提取物和精油)从2016年到2021年发现,以及它们降低细菌耐药性的潜力。他们对抗细菌的活动,特别强调多重耐药细菌,行动机制,与传统抗生素的可能组合,讨论了在当前医学中的作用和未来的前景。
    方法:对植物源化合物的抗菌活性及其对细菌作用机理的研究进行了鉴定和总结,包括2016年1月至2021年1月的捐款。使用PubMed搜索引擎以及相关关键字和运算符从Medline数据库中提取文章。
    结果:搜索产生了来自149个国家的11,689篇文章,其中101篇文章被纳入这篇综述。包括来自20个家庭的41种植物化学物质的报告。还包括来自17个科的39种植物的植物提取物和精油的报告。多酚和萜烯是研究的最活跃的植物化学物质,单独或作为植物提取物或精油的一部分。质膜破坏是最常见的抗菌作用机制。酚羟基的数量和位置,双键,在类黄酮的情况下,离域电子和与糖的共轭似乎对抗菌能力至关重要。植物化学物质与β-内酰胺抗生素的组合是研究最多的,外排泵的抑制是最常见的协同机制。
    结论:近年来,萜烯,黄酮,黄酮醇和一些生物碱和苯丙素,分离或作为提取物的一部分,已经显示出有希望的抗菌活性,被膜破坏它们最常见的机制。然而,需要通过新的组学技术和网络药理学来提高它们作为适当抗微生物药物的利用率,以找到其中最有效的组合或与抗生素的组合。
    BACKGROUND: Antibiotic-resistant bacteria pose a global health threat. Traditional antibiotics can lose their effectiveness, and the development of novel effective antimicrobials has become a priority in recent years. In this area, plants represent an invaluable source of antimicrobial compounds with vast therapeutic potential.
    OBJECTIVE: To review the full possible spectrum of plant antimicrobial agents (plant compounds, extracts and essential oils) discovered from 2016 to 2021 and their potential to decrease bacterial resistance. Their activities against bacteria, with special emphasis on multidrug resistant bacteria, mechanisms of action, possible combinations with traditional antibiotics, roles in current medicine and future perspectives are discussed.
    METHODS: Studies focusing on the antimicrobial activity of compounds of plant origin and their mechanism of action against bacteria were identified and summarized, including contributions from January 2016 until January 2021. Articles were extracted from the Medline database using PubMed search engine with relevant keywords and operators.
    RESULTS: The search yielded 11,689 articles from 149 countries, of which 101 articles were included in this review. Reports from 41 phytochemicals belonging to 20 families were included. Reports from plant extracts and essential oils from 39 plant species belonging to 17 families were also included. Polyphenols and terpenes were the most active phytochemicals studied, either alone or as a part of plant extracts or essential oils. Plasma membrane disruption was the most common mechanism of antimicrobial action. Number and position of phenolic hydroxyl groups, double bonds, delocalized electrons and conjugation with sugars in the case of flavonoids seemed to be crucial for antimicrobial capacity. Combinations of phytochemicals with beta-lactam antibiotics were the most studied, and the inhibition of efflux pumps was the most common synergistic mechanism.
    CONCLUSIONS: In recent years, terpenes, flavones, flavonols and some alkaloids and phenylpropanoids, either isolated or as a part of extracts, have shown promising antimicrobial activity, being membrane disruption their most common mechanism. However, their utilization as appropriate antimicrobials need to be boosted by means of new omics technologies and network pharmacology to find the most effective combinations among them or in combination with antibiotics.
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  • 文章类型: Journal Article
    印度尼西亚的心态一直专注于使用天然药物,食物,和治愈的做法被国家的文化广泛认可。传统医学中使用的传统药物和草药通常会导致发现针对某些疾病的药物。这篇综述的目的是研究关于Sembung植物重要性的循证数据,Blumeabalsamifera,作为一种潜在的传统医学。分布,民族药理学,次生代谢产物,和对几种疾病的生物活性是本综述的重点。使用术语“B.”搜索与Sembung工厂相关的信息和研究。balsamifera,\"\"植物化学物质,“和”药理活性“关于研究之门,谷歌学者,科学直接,PubMed,和2020年之前基于科学信息的数据库。一些民族医学文章推荐B.balsamifera治疗鼻窦炎,绞痛,咳嗽,肾结石,流感,或者作为利尿剂.这些知识已经在东南亚的几个国家得到了应用。B.balsamifera已被报道含有几种植物化学物质挥发性(萜类,脂肪酸,酚类物质,酒精,醛类,醚,酮,吡啶,呋喃,和烷烃)和非挥发性(类黄酮,黄烷酮,和查尔酮)。B.balsamifera的提取物和植物化学物质含有几种生物能力,如抗氧化剂,抗菌,抗真菌药,抗炎,降血脂,抗不孕,肝保护活性,抗糖尿病药,胃保护,抗肿瘤,抗癌,和针对冠状病毒病-19感染的免疫调节剂。这篇综述为balsamifica作为营养食品或未来药物制剂的潜在应用提供了必要的数据。
    Indonesia\'s mindset has been focusing on the use of natural medicines, food, and healing practices widely recognized by the nation\'s culture. Traditional medicines and herbs used in traditional medicine can often lead to the discovery of drugs against certain diseases. The aim of this review was to study evidence-based data on the importance of Sembung plant, Blumea balsamifera, as a potential traditional medicine. The distribution, ethnopharmacology, secondary metabolites, and bioactivity against several diseases are focused in this review. Information and research related to Sembung plant were searched using the terms \"B. balsamifera,\" \"phytochemicals,\" and \"pharmacological activity\" on ResearchGate, Google Scholar, Science Direct, PubMed, and scientific information-based databases up to 2020. Several ethnomedical articles recommend B. balsamifera for the treatment of sinusitis, colic pain, cough, kidney stones, flu, or as a diuretic. This knowledge has already been applied in several countries in Southeast Asia. B. balsamifera has been reported to contain several phytochemicals both volatile (terpenoids, fatty acids, phenols, alcohol, aldehydes, ethers, ketones, pyridines, furans, and alkanes) and non-volatile (flavonoids, flavanones, and chalcones). Extracts and phytochemicals of B. balsamifera contain several biological capacities such as antioxidant, antimicrobial, antifungal, anti-inflammatory, hypolipidemic, anti-infertility, hepatoprotective activity, antidiabetic, gastroprotective, antitumor, anticancer, and immunomodulatory agent against Coronavirus disease-19 infection. This review provides essential data for the potential application of B. balsamifera as a nutraceutical or in future medicinal preparations.
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  • 文章类型: Journal Article
    耐药菌对全球人类健康构成严重威胁。目前的抗生素正在失去功效,迫切需要新的抗微生物剂。活生物体是抗菌化合物的宝贵来源。最具代表性的动物天然产物的抗菌活性,细菌,本文对真菌和植物起源进行了综述。他们对耐药细菌的活性,他们的行动机制,抵抗他们的可能发展,讨论了他们在当前医学中的作用和未来的前景。电子数据库,如PubMed,Scopus和ScienceDirect用于搜索科学贡献,直到2020年9月,使用相关关键字。异质来源的天然化合物已被证明具有抗菌能力,包括对抗抗生素抗性细菌.最常见的抗微生物作用机制与蛋白质生物合成和细胞壁和膜的改变有关。各种天然化合物,尤其是植物化学物质,已显示出与抗生素的协同能力。关于开发针对天然抗微生物化合物的特异性抗性机制的文献很少。新技术,如组学,网络药理学和信息学有可能在未来鉴定和表征新的天然抗菌化合物。这些知识可能有助于制定未来的治疗策略。
    Drug-resistant bacteria pose a serious threat to human health worldwide. Current antibiotics are losing efficacy and new antimicrobial agents are urgently needed. Living organisms are an invaluable source of antimicrobial compounds. The antimicrobial activity of the most representative natural products of animal, bacterial, fungal and plant origin are reviewed in this paper. Their activity against drug-resistant bacteria, their mechanisms of action, the possible development of resistance against them, their role in current medicine and their future perspectives are discussed. Electronic databases such as PubMed, Scopus and ScienceDirect were used to search scientific contributions until September 2020, using relevant keywords. Natural compounds of heterogeneous origins have been shown to possess antimicrobial capabilities, including against antibiotic-resistant bacteria. The most commonly found mechanisms of antimicrobial action are related to protein biosynthesis and alteration of cell walls and membranes. Various natural compounds, especially phytochemicals, have shown synergistic capacity with antibiotics. There is little literature on the development of specific resistance mechanisms against natural antimicrobial compounds. New technologies such as -omics, network pharmacology and informatics have the potential to identify and characterize new natural antimicrobial compounds in the future. This knowledge may be useful for the development of future therapeutic strategies.
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