期刊论文详细信息
BMC Systems Biology
Molecular signatures for obesity and associated disorders identified through partial least square regression models
Samrat Chatterjee1  Kanury VS Rao2  Dhiraj Kumar2  Kamiya Tikoo2  Simarjeet Kaur Negi2  Parul Tripathi2  Sachin Sharma2  Neeraj Sinha2 
[1] Present address: Drug Discovery Research Centre, Translational Health Science & Technology Institute, Gurgaon 122016, India;Immunology Group, International Centre for Genetic Engineering and Biotechnology, Aruna, Asaf Ali Marg, New Delhi 110067, India
关键词: Hub-proteins;    Biological classifications;    Partial least square model;    Gene signature;    Type-II diabetes;    Obesity;   
Others  :  1127084
DOI  :  10.1186/s12918-014-0104-4
 received in 2012-07-18, accepted in 2014-08-18,  发布年份 2014
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【 摘 要 】

Background

Obesity is now a worldwide epidemic disease and poses a major risk for diet related diseases like type 2 diabetes, cardiovascular disease, stroke and fatty liver among others. In the present study we employed the murine model of diet-induced obesity to determine the early, tissue-specific, gene expression signatures that characterized progression to obesity and type 2 diabetes.

Results

We used the C57BL/6 J mouse which is known as a counterpart for diet-induced human diabetes and obesity model. Our initial experiments involved two groups of mice, one on normal diet (ND) and the other on high-fat and high-sucrose (HFHSD). The later were then further separated into subgroups that either received no additional treatment, or were treated with different doses of the Ayurvedic formulation KAL-1. At different time points (week3, week6, week9, week12, week15 and week18) eight different tissues were isolated from mice being fed on different diet compositions. These tissues were used to extract gene-expression data through microarray experiment. Simultaneously, we also measured different body parameters like body weight, blood Glucose level and cytokines profile (anti-inflammatory & pro-inflammatory) at each time point for all the groups.

Using partial least square discriminant analysis (PLS-DA) method we identified gene-expression signatures that predict physiological parameters like blood glucose levels, body weight and the balance of pro- versus anti-inflammatory cytokines. The resulting models successfully predicted diet-induced changes in body weight and blood glucose levels, although the predictive power for cytokines profiles was relatively poor. In the former two instances, however, we could exploit the models to further extract the early gene-expression signatures that accurately predict the onset of diabetes and obesity. These extracted genes allowed definition of the regulatory network involved in progression of disease.

Conclusion

We identified the early gene-expression signature for the onset of obesity and type 2 diabetes. Further analysis of this data suggests that some of these genes could be used as potential biomarkers for these two disease-states.

【 授权许可】

   
2014 Sinha et al.; licensee BioMed Central; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1][http://www.who.int/nmh/publications/ncd_report2010/en/] webcite Alwan A: The World Health Report..
  • [2]Hill JO, Peters JC, Catenacci VA, Wyatt HR: International strategies to address obesity. Obes Rev 2008, 9(Suppl 1):41-47.
  • [3]Haslam DW, James WPT: Obesity. Lancet 2005, 366(9492):1197-1209.
  • [4]Kopelman PG: Obesity as a medical problem. Nature 2000, 404(6778):635-643.
  • [5]Shao W, Yu Z, Chiang Y, Yang Y, Chai T, Foltz W, Lu H, Fantus IG, Jin T: Curcumin prevents high fat diet induced insulin resistance and obesity via attenuating lipogenesis in liver and inflammatory pathway in adipocytes. PLoS One 2012, 7(1):e28784.
  • [6]Tikoo K, Misra S, Rao KV, Tripathi P, Sharma S: Immunomodulatory Role of an Ayurvedic Formulation on Imbalanced Immunometabolics during Inflammatory Responses of Obesity and Prediabetic Disease. Evid base Compl Alternative Med 2013, 2013:795072.
  • [7]Perez-Enciso M, Tenenhaus M: Prediction of clinical outcome with microarray data: a partial least squares discriminant analysis (PLS-DA) approach. Hum Genet 2003, 112(5–6):581-592.
  • [8]Lin S, Thomas TC, Storlien LH, Huang XF: Development of high fat diet-induced obesity and leptin resistance in C57Bl/6 J mice. Int J Obes Relat Metab Disord 2000, 24(5):639-646.
  • [9]Petro AE, Cotter J, Cooper DA, Peters JC, Surwit SJ, Surwit RS: Fat, carbohydrate, and calories in the development of diabetes and obesity in the C57BL/6 J mouse. Metabolism 2004, 53(4):454-457.
  • [10]Surwit RS, Feinglos MN, Rodin J, Sutherland A, Petro AE, Opara EC, Kuhn CM, Rebuffe-Scrive M: Differential effects of fat and sucrose on the development of obesity and diabetes in C57BL/6 J and A/J mice. Metabolism 1995, 44(5):645-651.
  • [11]Staehr P, Hother-Nielsen O, Beck-Nielsen H: The role of the liver in type 2 diabetes. Rev Endocr Metab Disord 2004, 5(2):105-110.
  • [12]Juge-Aubry CE, Henrichot E, Meier CA: Adipose tissue: a regulator of inflammation. Best Pract Res Clin Endocrinol Metab 2005, 19(4):547-566.
  • [13]Lin Y, Sun Z: Current views on type 2 diabetes. J Endocrinol 2010, 204(1):1-11.
  • [14]Barabasi AL, Albert R: Emergence of scaling in random networks. Science 1999, 286(5439):509-512.
  • [15]Korhonen O, Matero S, Poso A, Ketolainen J: Partial least square projections to latent structures analysis (PLS) in evaluating and predicting drug release from starch acetate matrix tablets. J Pharm Sci 2005, 94(12):2716-2730.
  • [16]Mi H, Thomas P: PANTHER pathway: an ontology-based pathway database coupled with data analysis tools. Methods Mol Biol 2009, 563:123-140.
  • [17]Przulj N, Corneil DG, Jurisica I: Modeling interactome: scale-free or geometric? Bioinformatics 2004, 20(18):3508-3515.
  • [18]Barabasi A-L, Oltvai ZN: Network biology: understanding the cell’s functional organization. Nat Rev Genet 2004, 5(2):101-113.
  • [19]Yook SH, Oltvai ZN, Barabasi AL: Functional and topological characterization of protein interaction networks. Proteomics 2004, 4(4):928-942.
  • [20]Dong J, Horvath S: Understanding network concepts in modules. BMC Syst Biol 2007, 1:24. BioMed Central Full Text
  • [21]Liang H, Li WH: MicroRNA regulation of human protein protein interaction network. RNA 2007, 13(9):1402-1408.
  • [22]Chung J, Nguyen AK, Henstridge DC, Holmes AG, Chan MH, Mesa JL, Lancaster GI, Southgate RJ, Bruce CR, Duffy SJ, Horvath I, Mestril R, Watt MJ, Hooper PL, Kingwell BA, Vigh L, Hevener A, Febbraio MA: HSP72 protects against obesity-induced insulin resistance. Proc Natl Acad Sci U S A 2008, 105(5):1739-1744.
  • [23]Lee JH, Ragolia L: AKT phosphorylation is essential for insulin-induced relaxation of rat vascular smooth muscle cells. Am J Physiol Cell Physiol 2006, 291(6):C1355-C1365.
  • [24]Shelton RC, Claiborne J, Sidoryk-Wegrzynowicz M, Reddy R, Aschner M, Lewis DA, Mirnics K: Altered expression of genes involved in inflammation and apoptosis in frontal cortex in major depression. Mol Psychiatry 2011, 16(7):751-762.
  • [25]Hotamisligil GS: Inflammation and metabolic disorders. Nature 2006, 444(7121):860-867.
  • [26]van Noort V, Snel B, Huynen MA: The yeast coexpression network has a small-world, scale-free architecture and can be explained by a simple model. EMBO Rep 2004, 5(3):280-284.
  • [27]Kaput J, Klein KG, Reyes EJ, Kibbe WA, Cooney CA, Jovanovic B, Visek WJ, Wolff GL: Identification of genes contributing to the obese yellow Avy phenotype: caloric restriction, genotype, diet x genotype interactions. Physiol Genomics 2004, 18(3):316-324.
  • [28]Jesmin J, Rashid MS, Jamil H, Hontecillas R, Bassaganya-Riera J: Gene regulatory network reveals oxidative stress as the underlying molecular mechanism of type 2 diabetes and hypertension. BMC Med Genomics 2010, 3(1):45. BioMed Central Full Text
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