天然提取酚类化合物的潜在抗骨肉瘤活性:范围综述

M. Kasiram, Hermizi Hapidin, H. Abdullah, A. Azlina
{"title":"天然提取酚类化合物的潜在抗骨肉瘤活性:范围综述","authors":"M. Kasiram, Hermizi Hapidin, H. Abdullah, A. Azlina","doi":"10.37231/ajmb.2022.6.s1.579","DOIUrl":null,"url":null,"abstract":"Chemotherapy is the standard treatment component for osteosarcoma alongside the surgery. Nevertheless, the survival rate of patients diagnosed with osteosarcoma has not changed over the past three decades. Phenolic compounds are widely reported for having anti-proliferative effects against various cancers including osteosarcoma. Based on the framework published by Arskey and O’Malley [1] this scoping review was conducted to map the published literature on the anti-osteosarcoma activity of the phenolic compounds. \n  \nInitially, a literature search was conducted from electronic databases like PubMed, Scopus, EBSCO, Google Scholar Science Direct, and Web of Science. Articles on anti-osteosarcoma activities of phenolic compounds that were published between January 2001 and May 2022 were retrieved. The review process was guided by the framework of systematic reviews and meta-analysis (PRISMA) [2].  \n  \nIn total, 3168 articles were retrieved from the literature search. After a thorough screening, 95 articles were included in the final analysis after met the inclusion criteria. Most of the studies were published between the year 2011 to 2022 (84.2%) and only a few were published between 2001 to 2010 (15.8%) (Table 1). Among the selected studies, 53 types of phenolic compounds were identified to have a promising anti-osteosarcoma activity. Curcumin (12.6%) was the most reported phenolic compound followed by quercetin (11.6%) and resveratrol (10.5%) (Table 2). All studies were utilised in-vitro studies (n = 95), and some also conducted in-vivo evaluations (n = 17). MG-63 (50.5%) was identified to be the most used cell line. Meanwhile, BALB/c nude mice (58.8%) was the most frequently used in the in-vivo evaluation. In this review, it was found that 13 studies analysed the combination between phenolic compounds and chemotherapeutic drugs with 53.8% of the analysis demonstrating synergistic effect. \nThe number of published articles on the anti-osteosarcoma activities of phenolic compounds has increased dramatically over the past 10 years. Phenolic compounds became the main choice in oncotherapy research as it represents a major secondary metabolite in the plant. In this review, all the selected articles utilised in-vitro studies, and only several studies conducted in-vivo evaluations. For the in-vitro study, MG-63 was most frequently used because this cell line was reported to have phenotypic stability [3]. For the in-vivo study, BALB/c nude mice was mostly used because the utilization of immunocompromised mice has become an essential tool in the drug evaluation for cancer to maintain the tumour pathological traits [4]. Even though most of the compounds showed a remarkable inhibitory effect in-vitro and in-vivo, no clinical trial study was reported. Combination analysis is one of the efforts to induce the effectiveness of the treatment. Seven studies reported the synergistic effect when phenolic compound was combined with chemotherapeutic drug. The synergistic effect is the most desired drug-drug interaction in the application of the combination treatment as it can induce treatment efficacy [5].  \n  \nIn conclusion, this scoping review indicated a significant increase in the evaluation of the anti-osteosarcoma activity of the phenolic compounds.  Yet, several research gaps are remaining to be investigated like combination analysis and further continuation of clinical trial study so that the development of phenolic compound-based drugs for osteosarcoma treatment can be realised soon. ","PeriodicalId":189900,"journal":{"name":"Asian Journal of Medicine and Biomedicine","volume":"88 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Potential Anti-Osteosarcoma Activity from Naturally Extracted Phenolic Compound: A Scoping Review\",\"authors\":\"M. Kasiram, Hermizi Hapidin, H. Abdullah, A. Azlina\",\"doi\":\"10.37231/ajmb.2022.6.s1.579\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Chemotherapy is the standard treatment component for osteosarcoma alongside the surgery. Nevertheless, the survival rate of patients diagnosed with osteosarcoma has not changed over the past three decades. Phenolic compounds are widely reported for having anti-proliferative effects against various cancers including osteosarcoma. Based on the framework published by Arskey and O’Malley [1] this scoping review was conducted to map the published literature on the anti-osteosarcoma activity of the phenolic compounds. \\n  \\nInitially, a literature search was conducted from electronic databases like PubMed, Scopus, EBSCO, Google Scholar Science Direct, and Web of Science. Articles on anti-osteosarcoma activities of phenolic compounds that were published between January 2001 and May 2022 were retrieved. The review process was guided by the framework of systematic reviews and meta-analysis (PRISMA) [2].  \\n  \\nIn total, 3168 articles were retrieved from the literature search. After a thorough screening, 95 articles were included in the final analysis after met the inclusion criteria. Most of the studies were published between the year 2011 to 2022 (84.2%) and only a few were published between 2001 to 2010 (15.8%) (Table 1). Among the selected studies, 53 types of phenolic compounds were identified to have a promising anti-osteosarcoma activity. Curcumin (12.6%) was the most reported phenolic compound followed by quercetin (11.6%) and resveratrol (10.5%) (Table 2). All studies were utilised in-vitro studies (n = 95), and some also conducted in-vivo evaluations (n = 17). MG-63 (50.5%) was identified to be the most used cell line. Meanwhile, BALB/c nude mice (58.8%) was the most frequently used in the in-vivo evaluation. In this review, it was found that 13 studies analysed the combination between phenolic compounds and chemotherapeutic drugs with 53.8% of the analysis demonstrating synergistic effect. \\nThe number of published articles on the anti-osteosarcoma activities of phenolic compounds has increased dramatically over the past 10 years. Phenolic compounds became the main choice in oncotherapy research as it represents a major secondary metabolite in the plant. In this review, all the selected articles utilised in-vitro studies, and only several studies conducted in-vivo evaluations. For the in-vitro study, MG-63 was most frequently used because this cell line was reported to have phenotypic stability [3]. For the in-vivo study, BALB/c nude mice was mostly used because the utilization of immunocompromised mice has become an essential tool in the drug evaluation for cancer to maintain the tumour pathological traits [4]. Even though most of the compounds showed a remarkable inhibitory effect in-vitro and in-vivo, no clinical trial study was reported. Combination analysis is one of the efforts to induce the effectiveness of the treatment. Seven studies reported the synergistic effect when phenolic compound was combined with chemotherapeutic drug. The synergistic effect is the most desired drug-drug interaction in the application of the combination treatment as it can induce treatment efficacy [5].  \\n  \\nIn conclusion, this scoping review indicated a significant increase in the evaluation of the anti-osteosarcoma activity of the phenolic compounds.  Yet, several research gaps are remaining to be investigated like combination analysis and further continuation of clinical trial study so that the development of phenolic compound-based drugs for osteosarcoma treatment can be realised soon. \",\"PeriodicalId\":189900,\"journal\":{\"name\":\"Asian Journal of Medicine and Biomedicine\",\"volume\":\"88 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-11-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Medicine and Biomedicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.37231/ajmb.2022.6.s1.579\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Medicine and Biomedicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37231/ajmb.2022.6.s1.579","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

化疗是骨肉瘤除手术外的标准治疗方法。然而,在过去的三十年里,骨肉瘤患者的存活率并没有改变。酚类化合物被广泛报道对包括骨肉瘤在内的各种癌症具有抗增殖作用。基于Arskey和O 'Malley bbb发表的框架,对已发表的酚类化合物抗骨肉瘤活性的文献进行了范围综述。最初,文献检索是在PubMed、Scopus、EBSCO、b谷歌Scholar Science Direct和Web of Science等电子数据库中进行的。检索2001年1月至2022年5月间发表的关于酚类化合物抗骨肉瘤活性的文章。审查过程以系统审查和荟萃分析(PRISMA)框架为指导。从文献检索中共检索到3168篇文章。经过全面筛选,95篇符合纳入标准的文章被纳入最终分析。大多数研究发表于2011年至2022年(84.2%),只有少数研究发表于2001年至2010年(15.8%)(表1)。在所选的研究中,53种酚类化合物被确定具有很有希望的抗骨肉瘤活性。姜黄素(12.6%)是报道最多的酚类化合物,其次是槲皮素(11.6%)和白藜芦醇(10.5%)(表2)。所有研究均采用体外研究(n = 95),有些研究也进行了体内评估(n = 17)。MG-63(50.5%)是使用最多的细胞系。同时,BALB/c裸鼠(58.8%)在体内评价中使用频率最高。在这篇综述中,我们发现有13篇研究分析了酚类化合物与化疗药物的联合作用,其中53.8%的分析显示了协同作用。在过去的十年中,关于酚类化合物抗骨肉瘤活性的文章数量急剧增加。酚类化合物成为肿瘤治疗研究的主要选择,因为它代表了植物中主要的次生代谢物。在本综述中,所有选定的文章都使用了体外研究,只有几项研究进行了体内评估。在体外研究中,MG-63是最常用的,因为据报道该细胞系具有表型稳定性[3]。在体内研究中,主要使用BALB/c裸鼠,因为利用免疫功能低下的小鼠已成为癌症药物评价中维持肿瘤病理特征[4]的重要工具。尽管大多数化合物在体外和体内均表现出显著的抑制作用,但尚未有临床试验研究报道。联合分析是诱导治疗效果的努力之一。7项研究报道了酚类化合物与化疗药物联用时的增效作用。协同效应是联合治疗应用中最期望的药物-药物相互作用,因为协同效应可以诱导治疗疗效bb0。总之,这一范围综述表明酚类化合物抗骨肉瘤活性的评价显著增加。然而,仍有一些研究空白有待研究,如联合分析和进一步的临床试验研究,以便早日实现以酚类化合物为基础的骨肉瘤治疗药物的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Potential Anti-Osteosarcoma Activity from Naturally Extracted Phenolic Compound: A Scoping Review
Chemotherapy is the standard treatment component for osteosarcoma alongside the surgery. Nevertheless, the survival rate of patients diagnosed with osteosarcoma has not changed over the past three decades. Phenolic compounds are widely reported for having anti-proliferative effects against various cancers including osteosarcoma. Based on the framework published by Arskey and O’Malley [1] this scoping review was conducted to map the published literature on the anti-osteosarcoma activity of the phenolic compounds.   Initially, a literature search was conducted from electronic databases like PubMed, Scopus, EBSCO, Google Scholar Science Direct, and Web of Science. Articles on anti-osteosarcoma activities of phenolic compounds that were published between January 2001 and May 2022 were retrieved. The review process was guided by the framework of systematic reviews and meta-analysis (PRISMA) [2].    In total, 3168 articles were retrieved from the literature search. After a thorough screening, 95 articles were included in the final analysis after met the inclusion criteria. Most of the studies were published between the year 2011 to 2022 (84.2%) and only a few were published between 2001 to 2010 (15.8%) (Table 1). Among the selected studies, 53 types of phenolic compounds were identified to have a promising anti-osteosarcoma activity. Curcumin (12.6%) was the most reported phenolic compound followed by quercetin (11.6%) and resveratrol (10.5%) (Table 2). All studies were utilised in-vitro studies (n = 95), and some also conducted in-vivo evaluations (n = 17). MG-63 (50.5%) was identified to be the most used cell line. Meanwhile, BALB/c nude mice (58.8%) was the most frequently used in the in-vivo evaluation. In this review, it was found that 13 studies analysed the combination between phenolic compounds and chemotherapeutic drugs with 53.8% of the analysis demonstrating synergistic effect. The number of published articles on the anti-osteosarcoma activities of phenolic compounds has increased dramatically over the past 10 years. Phenolic compounds became the main choice in oncotherapy research as it represents a major secondary metabolite in the plant. In this review, all the selected articles utilised in-vitro studies, and only several studies conducted in-vivo evaluations. For the in-vitro study, MG-63 was most frequently used because this cell line was reported to have phenotypic stability [3]. For the in-vivo study, BALB/c nude mice was mostly used because the utilization of immunocompromised mice has become an essential tool in the drug evaluation for cancer to maintain the tumour pathological traits [4]. Even though most of the compounds showed a remarkable inhibitory effect in-vitro and in-vivo, no clinical trial study was reported. Combination analysis is one of the efforts to induce the effectiveness of the treatment. Seven studies reported the synergistic effect when phenolic compound was combined with chemotherapeutic drug. The synergistic effect is the most desired drug-drug interaction in the application of the combination treatment as it can induce treatment efficacy [5].    In conclusion, this scoping review indicated a significant increase in the evaluation of the anti-osteosarcoma activity of the phenolic compounds.  Yet, several research gaps are remaining to be investigated like combination analysis and further continuation of clinical trial study so that the development of phenolic compound-based drugs for osteosarcoma treatment can be realised soon. 
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信