Copper in colorectal cancer patients: a systematic review and meta-analysis.

IF 2.9 3区 医学 Q2 ONCOLOGY Carcinogenesis Pub Date : 2025-01-20 DOI:10.1093/carcin/bgaf001
Carlos Muñoz-Bravo, Inés Marín-Burdallo, Lucas González-Herrera, Carla González-Palacios Torres, Macarena Lozano-Lorca, José Juan Jiménez-Moleón, Rocío Olmedo-Requena
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Abstract

Several clinical studies have evaluated the relationship between copper on colorectal cancer (CRC), but the results are contradictory. This study aimed to conduct a systematic review and meta-analysis to investigate copper measured in two biological matrices (serum/plasma/blood and tissue) and dietary intake in CRC patients compared to healthy controls. We conducted a comprehensive and systematic search in PubMed, Scopus, Embase, and Web of Science. We included studies that reported copper levels in serum/plasma/blood, tissue, or from the diet, with an observational study design (cohort and case-control studies). Study quality was assessed with the Newcastle-Ottawa scale and potential causes of heterogeneity were evaluated. Standardized mean differences (SMD) with 95% confidence interval (CI) were pooled using random-effect models. Overall pooled odds ratio and 95% CI for the risk of CRC were calculated. Twenty-six studies (23 case-control and 3 cohort studies) with a total of 227 354 participants were included. Most of the studies presented low (50%) or moderate quality (42.3%). No differences in serum/plasma/blood copper levels (SMD = 0.23; 95% CI: -0.23, 0.70; I2 = 97.3%, 19 studies), tissue copper levels (SMD = -1.69; 95% CI: -3.41, 0.03; I2 = 85.6%, 2 studies), or copper/zinc ratio (SMD = 1.19; 95% CI: 0.54, 1.84; I2 = 95.3%, 6 studies) were found between CRC patients and healthy controls. Regarding dietary copper, CRC patients had a lower intake (SMD = -0.27; 95% CI: -0.51, -0.03; I2 = 0.0%, 2 studies). No differences were found in copper levels between CRC patients and healthy controls. However, evidence shows mostly low or moderate quality, and results were heterogeneous. More prospective studies with an adequate methodological approach are needed.

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铜在结直肠癌患者中的作用:一项系统综述和荟萃分析。
一些临床研究评估了铜与结直肠癌(CRC)之间的关系,但结果相互矛盾。本研究旨在对两种生物基质(血清/血浆/血液和组织)和CRC患者饮食中铜含量与健康对照进行系统回顾和荟萃分析。我们在PubMed, Scopus, Embase和Web of Science中进行了全面系统的检索。我们纳入了报道血清/血浆/血液、组织或饮食中铜水平的研究,并采用观察性研究设计(队列研究和病例对照研究)。用纽卡斯尔-渥太华量表评估研究质量,并评估异质性的潜在原因。采用随机效应模型合并95%置信区间(CI)的标准化平均差(SMD)。计算结直肠癌风险的总合并优势比和95% CI。纳入26项研究(23项病例对照研究和3项队列研究),共227,354名受试者。大多数研究呈现低质量(50%)或中等质量(42.3%)。血清/血浆/血铜水平无差异(SMD=0.23;95%ci -0.23, 0.70;I2=97.3%, 19项研究),组织铜水平(SMD=-1.69;95%ci -3.41, 0.03;I2=85.6%, 2项研究),或铜/锌比(SMD=1.19;95%ci 0.54, 1.84;(2=95.3%, 6项研究)。在膳食铜方面,结直肠癌患者的铜摄入量较低(SMD=-0.27;95%ci -0.51, -0.03;I2=0.0%, 2项研究)。在结直肠癌患者和健康对照者之间没有发现铜水平的差异。然而,证据显示大多是低质量或中等质量,结果是异质性的。需要更多具有适当方法学方法的前瞻性研究。
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来源期刊
Carcinogenesis
Carcinogenesis 医学-肿瘤学
CiteScore
9.20
自引率
2.10%
发文量
95
审稿时长
1 months
期刊介绍: Carcinogenesis: Integrative Cancer Research is a multi-disciplinary journal that brings together all the varied aspects of research that will ultimately lead to the prevention of cancer in man. The journal publishes papers that warrant prompt publication in the areas of Biology, Genetics and Epigenetics (including the processes of promotion, progression, signal transduction, apoptosis, genomic instability, growth factors, cell and molecular biology, mutation, DNA repair, genetics, etc.), Cancer Biomarkers and Molecular Epidemiology (including genetic predisposition to cancer, and epidemiology), Inflammation, Microenvironment and Prevention (including molecular dosimetry, chemoprevention, nutrition and cancer, etc.), and Carcinogenesis (including oncogenes and tumor suppressor genes in carcinogenesis, therapy resistance of solid tumors, cancer mouse models, apoptosis and senescence, novel therapeutic targets and cancer drugs).
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