Cave Matthew C, Pinkston Christina M, Rai Shesh N, Wahlang Banrida, Pavuk Marian, Head Kimberly Z, Carswell Gleta K, Nelson Gail M, Klinge Carolyn M, Bell Douglas A, Birnbaum Linda S, Chorley Brian N
Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, School of Medicine, University of Louisville, Louisville, Kentucky, USA.
Department of Pharmacology & Toxicology, School of Medicine, University of Louisville, Louisville, Kentucky, USA.
Environ Health Perspect. 2022 Jan;130(1):17003. doi: 10.1289/EHP9467. Epub 2022 Jan 6.
Polychlorinated biphenyl (PCB) exposures have been associated with liver injury in human cohorts, and steatohepatitis with liver necrosis in model systems. MicroRNAs (miRs) maintain cellular homeostasis and may regulate the response to environmental stress.
We tested the hypothesis that specific miRs are associated with liver disease and PCB exposures in a residential cohort.
Sixty-eight targeted hepatotoxicity miRs were measured in archived serum from 734 PCB-exposed participants in the cross-sectional Anniston Community Health Survey. Necrotic and other liver disease categories were defined by serum keratin 18 (K18) biomarkers. Associations were determined between exposure biomarkers (35 ortho-substituted PCB congeners) and disease biomarkers (highly expressed miRs or previously measured cytokines), and Ingenuity Pathway Analysis was performed.
The necrotic liver disease category was associated with four up-regulated miRs (miR-99a-5p, miR-122-5p, miR-192-5p, and miR-320a) and five down-regulated miRs (let-7d-5p, miR-17-5p, miR-24-3p, miR-197-3p, and miR-221-3p). Twenty-two miRs were associated with the other liver disease category or with K18 measurements. Eleven miRs were associated with 24 PCBs, most commonly congeners with anti-estrogenic activities. Most of the exposure-associated miRs were associated with at least one serum hepatocyte death, pro-inflammatory cytokine or insulin resistance bioarker, or with both. Within each biomarker category, associations were strongest for the liver-specific miR-122-5p. Pathways of liver toxicity that were identified included inflammation/hepatitis, hyperplasia/hyperproliferation, cirrhosis, and hepatocellular carcinoma. Tumor protein p53 and tumor necrosis factor were well integrated within the top identified networks.
These results support the human hepatotoxicity of environmental PCB exposures while elucidating potential modes of PCB action. The MiR-derived liquid liver biopsy represents a promising new technique for environmental hepatology cohort studies. https://doi.org/10.1289/EHP9467.
多氯联苯(PCB)暴露与人类队列中的肝损伤以及模型系统中的脂肪性肝炎伴肝坏死有关。微小RNA(miR)维持细胞内稳态,并可能调节对环境应激的反应。
我们检验了一个假设,即在一个居住队列中,特定的miR与肝脏疾病和PCB暴露有关。
在横断面安尼斯顿社区健康调查中,对734名PCB暴露参与者的存档血清中68种靶向肝毒性miR进行了测量。坏死性和其他肝脏疾病类别由血清角蛋白18(K18)生物标志物定义。确定了暴露生物标志物(35种邻位取代的PCB同系物)与疾病生物标志物(高表达的miR或先前测量的细胞因子)之间的关联,并进行了 Ingenuity 通路分析。
坏死性肝病类别与4种上调的miR(miR-99a-5p、miR-122-5p、miR-192-5p和miR-320a)以及5种下调的miR(let-7d-5p、miR-17-5p、miR-24-3p、miR-197-3p和miR-221-3p)相关。22种miR与其他肝脏疾病类别或K18测量值相关。11种miR与24种PCB相关,最常见的是具有抗雌激素活性的同系物。大多数与暴露相关的miR与至少一种血清肝细胞死亡、促炎细胞因子或胰岛素抵抗生物标志物相关,或与两者都相关。在每个生物标志物类别中,肝脏特异性miR-122-5p的关联最强。确定的肝脏毒性途径包括炎症/肝炎、增生/过度增殖、肝硬化和肝细胞癌。肿瘤蛋白p53和肿瘤坏死因子在确定的顶级网络中得到了很好的整合。
这些结果支持环境PCB暴露对人类的肝毒性,同时阐明了PCB作用的潜在模式。基于miR的液体肝脏活检代表了环境肝脏病队列研究中一种有前途的新技术。https://doi.org/10.1289/EHP9467。