Targeting the Circulating MicroRNA Signature of Obesity

Author:

Ortega Francisco José12,Mercader Josep María3,Catalán Victoria24,Moreno-Navarrete José María12,Pueyo Neus12,Sabater Mónica1,Gómez-Ambrosi Javier24,Anglada Roger5,Fernández-Formoso José Antonio2,Ricart Wifredo12,Frühbeck Gema24,Fernández-Real José Manuel12

Affiliation:

1. Department of Diabetes, Endocrinology and Nutrition, Institut d'Investigació Biomédica de Girona, Girona, Spain

2. Centro de Investigación Biomédica en Red de la Fisiopatología de la Obesidad y la Nutrición (CB06/03) and Instituto de Salud Carlos III, Santiago de Compostela, Spain

3. Joint Institute for Research in Biomedicine-Barcelona Supercomputing Center Program on Computational Biology, Barcelona, Spain

4. Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain; and

5. Genome Facility Core Service, Universitat Pompeu Fabra, Barcelona, Spain

Abstract

BACKGROUND Genomic studies have yielded important insights into the pathogenesis of obesity. Circulating microRNAs (miRNAs) are valuable biomarkers of systemic diseases and potential therapeutic targets. We sought to define the circulating pattern of miRNAs in obesity and examine changes after weight loss. METHODS We assessed the genomewide circulating miRNA profile cross-sectionally in 32 men and after surgery-induced weight loss in 6 morbidly obese patients. The most relevant miRNAs were cross-sectionally validated in 80 men and longitudinally in 22 patients (after surgery-induced weight loss). We evaluated the effects of diet-induced weight loss in 9 obese patients. Thirty-six circulating miRNAs were associated with anthropometric variables in the initial sample. RESULTS In the validation study, morbidly obese patients showed a marked increase of miR-140-5p, miR-142-3p (both P < 0.0001), and miR-222 (P = 0.0002) and decreased levels of miR-532–5p, miR-125b, miR-130b, miR-221, miR-15a, miR-423-5p, and miR-520c-3p (P < 0.0001 for all). Interestingly, in silico targets leukemia inhibitory factor receptor (LIFR) and transforming growth factor receptor (TGFR) of miR-140-5p, miR-142-3p, miR-15a, and miR-520c-3p circulated in association with their corresponding miRNAs. Moreover, a discriminant function of 3 miRNAs (miR-15a, miR-520c-3p, and miR-423-5p) was specific for morbid obesity, with an accuracy of 93.5%. Surgery-induced (but not diet-induced) weight loss led to a marked decrease of miR-140-5p, miR-122, miR-193a-5p, and miR-16-1 and upregulation of miR-221 and miR-199a-3p (P < 0.0001 for all). CONCLUSIONS Circulating miRNAs are deregulated in severe obesity. Weight loss–induced changes in this profile and the study of in silico targets support this observation and suggest a potential mechanistic relevance.

Funder

Associació Catalana de Diabetis

Instituto de Salud Carlos III

Spanish Ministry of Science and Innovation

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Reference40 articles.

1. Overweight, obesity and cancer: epidemiological evidence and proposed mechanisms;Calle;Nat Rev Cancer,2004

2. Obesity and the regulation of energy balance;Spiegelman;Cell,2001

3. New-generation high-throughput technologies based ‘omics’ research strategy in human disease (in Chinese);Yang;Yi Chuan,2011

4. MicroRNAs: key players in the immune system, differentiation, tumorigenesis and cell death;Schickel;Oncogene,2008

5. MicroRNAs and cancer: role in tumorigenesis, patient classification and therapy;Hernando;Clin Transl Oncol,2007

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3