目的 分析血浆中表皮生长因子受体3(ErbB3)蛋白表达水平与超重的相关性,探讨ErbB3在超重中的作用。方法 招募2019 年7-8月于弋矶山医院体检中心的128名33~79岁成年人,按体质量指数(BMI)≥24.0 Kg/m2 为超重组,BMI<24.0 Kg/m2为对照组,采集研究对象血液样本,使用酶联免疫吸附法(ELISA) 检测血浆ErbB3蛋白。结果 男性研究对象,超重组血浆ErbB3蛋白水平低于对照组;饮酒人群中,超重组ErbB3蛋白水平也明显降低,差异均具有统计学意义(P<0.05)。ErbB3水平在男性(r=-0.252,P=0.034)、饮酒人群(r=-0.389,P =0.008)中与BMI呈负相关。结论 ErbB3水平降低与成人超重相关,但仅限于男性和饮酒的人群。
Abstract
Objective To analyze the correlation between the expression of epidermal growth factor receptor 3 (ErbB3) protein in plasma and overweight,and to explore the role of ErbB3 in overweight. Methods 128 adults aged 33-79 were recruited from the physical examination center of Yijishan hospital from July to August in 2019. Body mass index (BMI) ≥24.0 Kg/m2 was used as overweight,and BMI<24.0 Kg/m2 was used as control. Plasma ErbB3 level was assessed by the Enzyme-linked immunosorbent assay (ELISA). Results In the male population,the plasma ErbB3 level in overweight group was lower than that in the control group. In the drinking population,the level of ErbB3 in overweight population was also significantly reduced,and the difference was statistically significant(P<0.05). The level of ErbB3 was negatively correlated with BMI in males(r = -0.252,P= 0.034)and drinking population(r=-0.389,P=0.008). Conclusion In males and drinkers,the decrease of ErbB3 level is associated with adult overweight.
关键词
ErbB3 /
表皮生长因子受体 /
超重 /
肥胖
Key words
ErbB3 /
Epidermal growth factor receptor /
Overweight /
Obesity
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参考文献
[1] NCD Risk Factor Collaboration(NCD-RisC).Trends in adult body-mass index in 200 countries from 1975 to 2014: a pooled analysis of 1698 population-based measurement studies with 19.2 million participants[J].Lancet,2016,387(10026): 1377-1396.
[2] 佚名.中国心血管健康与疾病报告2019概要[J].中国循环杂志,2020,35(09): 833-854.
[3] Coussens L,Yang-FENG TL,Liao YC,et al.Tyrosine kinase receptor with extensive homology to EGF receptor shares chromosomal location with neu oncogene[J].Science,1985,230(4730): 1132-1139.
[4] Ray A.Tumor-linked HER2 expression: association with obesity and lipid-related microenvironment[J].Hormone molecular biology and clinical investigation,2017,32(3):1-18.
[5] Yarden Y,Sliwkowski MX.Untangling the ErbB signalling network[J].Nature reviews Molecular cell biology,2001,2(2): 127-137.
[6] Shif F,Telesco SE,Liu YT,et al.ErbB3/HER3 intracellular domain is competent to bind ATP and catalyze autophosphorylation[J].Proceedings of the National Academy of Sciences of the United States of America,2010,7692-7697.
[7] Tzahar E,Waterman H,Chen X,et al.A hierarchical network of interreceptor interactions determines signal transduction by Neu differentiation factor/neuregulin and epidermal growth factor[J].Molecular and cellular biology,1996,16(10): 5276-5287.
[8] Russell KS,Kalinowski A,Hedhli N.Cardiovascular Effects of Neuregulin-1/ErbB Signaling: Role in Vascular Signaling and Angiogenesis[J].Current Pharmaceutical Design,2014,20(30):4899-4905.
[9] Rebecca,Kanter,Benjamin,et al.Global Gender Disparities in Obesity: A Review[J].Advances in Nutrition,2012:491-498.
[10] Traversy G,Chaput J P.Alcohol Consumption and Obesity: An Update[J].Current obesity reports,2015,4(1): 122-130.
[11] Stern C,Schreier B,Nolze A,et al.Knockout of vascular smooth muscle EGF receptor in a mouse model prevents obesity-induced vascular dysfunction and renal damage in vivo[J].Diabetologia,2020,63(2): 1-17.
[12] Scioli MG,Cervelli V,Arcuri G,et al.High insulin-induced down-regulation of Erk-1/IGF-1R/FGFR-1 signaling is required for oxidative stress-mediated apoptosis of adipose-derived stem cells[J].Journal of Cellular Physiology,2015,229(12): 2077-2087.
[13] Wang GX,Zhao XY,Meng ZX,et al.The brown fat-enriched secreted factor Nrg4 preserves metabolic homeostasis through attenuation of hepatic lipogenesis[J].Nature Medicine,2014,20(12): 1436.
[14] Ottolini M,Hong K,Cope EL,et al.Local Peroxynitrite Impairs Endothelial Transient Receptor Potential Vanilloid 4 Channels and Elevates Blood Pressure in Obesity[J].Circulation,2020,141(16): 1318-1333.
[15] Saifeddine M,El-Daly M,Mihara K,et al.GPCR‐mediated EGF receptor transactivation regulates TRPV4 action in the vasculature[J].British Journal of Pharmacology,2015,172(10):2493-2506.
基金
安徽省教育厅高校自然科学研究重点项目(KJ2019A0405:KJ2019A0404);国家卫生健康委员会卫生经济与政策研究重点实验室开放课题(NHC-HEPR2019001); 安徽省重点研究与开发计划(1804h08020261);安徽省自然科学基金项目(1808085QH283)