Percario Rossana, Panaccio Paolo, di Mola Fabio Francesco, Grottola Tommaso, Di Sebastiano Pierluigi
General Surgery Unit, "F. Renzetti" Hospital, 66034 Lanciano, Italy.
Division of Surgical Oncology, Clinica Pierangeli, 65124 Pescara, Italy.
Cancers (Basel). 2021 Dec 12;13(24):6237. doi: 10.3390/cancers13246237.
colorectal cancer (CRC) has a multifactorial etiology which comprises microbiota, genetic predisposition, diet, environmental factors, and last but not least, a substantial contribution by inflammation. The aim of this study is to conduct a systematic review of the literature regarding the strong link between inflammation and colorectal cancer.
A systematic review of the literature on PubMed (Medline), Scopus, Cochrane and EMBase databases was performed, following the PRISMA 2020 guidelines. Each paper was reviewed by two groups of researchers in a single-blind format by using a pre-planned Microsoft Excel grid.
Using automated research filters, 14,566 studies were included, but 1% was found significant by the reviewers. Seventy pathways of inflammation were described in the sequence of inflammation-carcinogenesis, and anti-tumorigenic molecules were also found.
several studies suggest a strong role of inflammation in the tumorigenesis of colorectal cancer through different pathways: this may have a diagnostic and clinical role and also therapeutic purpose in preventing carcinogenesis by treating inflammation. In vitro tests support this theory, even if many other clinical trials are necessary. The present paper was registered in the OpenScience Framework registry (Identifier: DOI 10.17605/OSF.IO/2KG7T).
结直肠癌(CRC)具有多因素病因,包括微生物群、遗传易感性、饮食、环境因素,以及最后但同样重要的是,炎症的重大影响。本研究的目的是对关于炎症与结直肠癌之间紧密联系的文献进行系统综述。
按照PRISMA 2020指南,对PubMed(Medline)、Scopus、Cochrane和EMBase数据库中的文献进行系统综述。每篇论文由两组研究人员采用预先规划好的Microsoft Excel表格以单盲形式进行评审。
使用自动研究筛选器,共纳入14566项研究,但评审人员发现其中1%具有显著性。在炎症 - 致癌过程中描述了70条炎症途径,并且还发现了抗肿瘤分子。
多项研究表明,炎症通过不同途径在结直肠癌的肿瘤发生中发挥重要作用:这在诊断和临床方面可能具有作用,并且在通过治疗炎症预防癌变方面也具有治疗意义。体外试验支持这一理论,尽管还需要许多其他临床试验。本文已在开放科学框架注册库中注册(标识符:DOI 10.17605/OSF.IO/2KG7T)。