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Effect of Curcumin on Aged Drosophila Melanogaster:A Pathway Prediction Analysis

Effect of Curcumin on Aged Drosophila Melanogaster:A Pathway Prediction Analysis
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摘要 Objective: To re-analyze the data published in order to explore plausible biological pathways that can be used to explain the anti-aging effect of curcumin. Methods: Microarray data generated from other study aiming to investigate effect of curcumin on extending lifespan of Drosophila melanogaster were further used for pathway prediction analysis. The differentially expressed genes were identified by using GeneSpdng GX with a criterion of 3.0-fold change. Two Cytoscape plugins including BisoGenet and molecular complex detection (MCODE) were used to establish the protein-protein interaction (PPI) network based upon differential genes in order to detect highly connected regions. The function annotation clustering tool of Database for Annotation, Visualization and Integrated Discovery (DAVID) was used for pathway analysis. Results: A total of 87 genes expressed differentially in D. melanogaster treated with curcumin were identified, among which 50 were up-regulated significantly and 37 were remarkably down-regulated in D. melanogaster treated with curcumin. Based upon these differential genes, PPI network was constructed with 1,082 nodes and 2,412 edges. Five highly connected regions in PPI networks were detected by MCODE algorithm, suggesting anti-aging effect of curcumin may be underlined through five different pathways including Notch signaling pathway, basal transcription factors, cell cycle regulation, ribosome, Wnt signaling pathway, and p53 pathway. Conclusion: Genes and their associated pathways in D. rnelanogaster treated with anti-aging agent curcumin were identified using PPI network and MCODE algorithm, suggesting that curnumin may be developed as an alternative therapeutic medicine for treating aging-associated diseases. Objective: To re-analyze the data published in order to explore plausible biological pathways that can be used to explain the anti-aging effect of curcumin. Methods: Microarray data generated from other study aiming to investigate effect of curcumin on extending lifespan of Drosophila melanogaster were further used for pathway prediction analysis. The differentially expressed genes were identified by using GeneSpdng GX with a criterion of 3.0-fold change. Two Cytoscape plugins including BisoGenet and molecular complex detection (MCODE) were used to establish the protein-protein interaction (PPI) network based upon differential genes in order to detect highly connected regions. The function annotation clustering tool of Database for Annotation, Visualization and Integrated Discovery (DAVID) was used for pathway analysis. Results: A total of 87 genes expressed differentially in D. melanogaster treated with curcumin were identified, among which 50 were up-regulated significantly and 37 were remarkably down-regulated in D. melanogaster treated with curcumin. Based upon these differential genes, PPI network was constructed with 1,082 nodes and 2,412 edges. Five highly connected regions in PPI networks were detected by MCODE algorithm, suggesting anti-aging effect of curcumin may be underlined through five different pathways including Notch signaling pathway, basal transcription factors, cell cycle regulation, ribosome, Wnt signaling pathway, and p53 pathway. Conclusion: Genes and their associated pathways in D. rnelanogaster treated with anti-aging agent curcumin were identified using PPI network and MCODE algorithm, suggesting that curnumin may be developed as an alternative therapeutic medicine for treating aging-associated diseases.
出处 《Chinese Journal of Integrative Medicine》 SCIE CAS CSCD 2015年第2期115-122,共8页 中国结合医学杂志(英文版)
基金 Supported by the National Natural Science Foundation of China(No.81102680) China Postdoctoral Science Foundation(No.20100470524)
关键词 ANTI-AGING CURCUMIN Drosophila Melanogaster pathway prediction analysis protein-protein interaction network anti-aging, curcumin, Drosophila Melanogaster, pathway prediction analysis, protein-protein interaction network
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  • 1Rose MR, Burke MK, Shahrestani P, Mueller LD. Evolution of ageing since darwin. J Genet 2008;87:363-371.
  • 2Mather KA, Jorm AF, Parslow RA, Christensen H. Is telomere length a biomarker of aging? A review. J Gerontol A Biol Sci Med Sci 2011 ;66:202-213.
  • 3Romano AD, Serviddio G, de Matthaeis A, Bellanti F, Vendemiale G. Oxidative stress and aging. J Nephrol 2010;23 (Suppl) 15:$29-$36.
  • 4Kang TH, Park HM, Kim YB, Kim H, Kim N, Do JH, et al. Effects of red ginseng extract on UVB irradiation- induced skin aging in hairless mice. J Ethnopharmacol 2009; 123:446-451.
  • 5Brousseau M, Miller SC. Enhancement of natural killer cells and increased survival of aging mice fed daily echinacea root extract from youth. Biogerontology 2005;6:157-163.
  • 6Jafari M. Drosophila melanogaster as a model system for the evaluation of anti-aging compounds. Fly (Austin) 2010;4:253-257.
  • 7Lee KS, Lee BS, Semnani S, Avanesian A, Um CY, Jeon H J, et al. Curcumin extends life span, improves health span, and modulates the expression of age-associated aging genes in drosophila melanogaster. Rejuvenation Res 2010; 13:561-570.
  • 8Gene expression omnibus (GEO). Bethesda: National center for biotechnology information (NCBI), U.S. National library of medicine, 2011 (accessed april 9, 2011 at http://www.Ncbi. NIm Nih. Gov /geo/query /acc. Cgi ? Acc=gse 21182. ).
  • 9Saldanha AJ. Java treeview-extensible visualization of microarray data. Bioinformatics 2004;20:3246-3248.
  • 10ReaI-Chicharro A, Ruiz-Mostazo I, Navas-Delgado I, Kerzazi A, Chniber O, Sanchez-Jimenez F, et al. Protopia: a protein-protein interaction tool. BMC Bioinformatics 2009;10 (Suppl) 12:$17.

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