Sampaio Laeza Alves, Pina Lícia Tairiny Santos, Serafini Mairim Russo, Tavares Débora Dos Santos, Guimarães Adriana Gibara
Graduate Program of Applied Sciences to Health, Federal University of Sergipe, Lagarto, Brazil.
Graduate Program in Health Sciences, Federal University of Sergipe, Aracaju, Brazil.
Front Pharmacol. 2021 Jul 7;12:702487. doi: 10.3389/fphar.2021.702487. eCollection 2021.
It is estimated that one in five people worldwide faces a diagnosis of a malignant neoplasm during their lifetime. Carvacrol and its isomer, thymol, are natural compounds that act against several diseases, including cancer. Thus, this systematic review aimed to examine and synthesize the knowledge on the antitumor effects of carvacrol and thymol. A systematic literature search was carried out in the PubMed, Web of Science, Scopus and Lilacs databases in April 2020 (updated in March 2021) based on the PRISMA 2020 guidelines. The following combination of health descriptors, MeSH terms and their synonyms were used: carvacrol, thymol, antitumor, antineoplastic, anticancer, cytotoxicity, apoptosis, cell proliferation, and . To assess the risk of bias in studies, the SYRCLE Risk of Bias tool was used, and for studies, a modified version was used. A total of 1,170 records were identified, with 77 meeting the established criteria. The studies were published between 2003 and 2021, with 69 being and 10 Forty-three used carvacrol, 19 thymol, and 15 studies tested both monoterpenes. It was attested that carvacrol and thymol induced apoptosis, cytotoxicity, cell cycle arrest, antimetastatic activity, and also displayed different antiproliferative effects and inhibition of signaling pathways (MAPKs and PI3K/AKT/mTOR). Carvacrol and thymol exhibited antitumor and antiproliferative activity through several signaling pathways. , carvacrol appears to be more potent than thymol. However, further studies with robust methodology are required to define a standard and safe dose, determine their toxic or side effects, and clarify its exact mechanisms of action. This systematic review was registered in the PROSPERO database (CRD42020176736) and the protocol is available at https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=176736.
据估计,全球五分之一的人在其一生中会面临恶性肿瘤的诊断。香芹酚及其异构体百里酚是对包括癌症在内的多种疾病有作用的天然化合物。因此,本系统综述旨在审视和综合关于香芹酚和百里酚抗肿瘤作用的知识。2020年4月(2021年3月更新),根据PRISMA 2020指南,在PubMed、科学网、Scopus和Lilacs数据库中进行了系统的文献检索。使用了以下健康描述词、医学主题词及其同义词的组合:香芹酚、百里酚、抗肿瘤、抗瘤、抗癌、细胞毒性、细胞凋亡、细胞增殖等。为评估研究中的偏倚风险,使用了SYRCLE偏倚风险工具,对于某些研究,则使用了修改版。共识别出1170条记录,其中77条符合既定标准。这些研究发表于2003年至2021年之间,69项为[此处信息缺失],10项为[此处信息缺失]。43项使用香芹酚,19项使用百里酚,15项研究对这两种单萜类化合物都进行了测试。证实香芹酚和百里酚可诱导细胞凋亡、细胞毒性、细胞周期阻滞、抗转移活性,并且还表现出不同的抗增殖作用以及对信号通路(丝裂原活化蛋白激酶和磷脂酰肌醇-3-激酶/蛋白激酶B/哺乳动物雷帕霉素靶蛋白)的抑制作用。香芹酚和百里酚通过多种信号通路展现出抗肿瘤和抗增殖活性。[此处信息缺失],香芹酚似乎比百里酚更有效。然而,需要进一步采用可靠方法的研究来确定标准和安全剂量,确定其毒性或副作用,并阐明其确切作用机制。本系统综述已在PROSPERO数据库(CRD42020176736)中注册,方案可在https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=176736获取。