FOLLOWUS
1. Institute of Basic Theory, China Academy of Chinese Medical Sciences,Beijing,China
2. Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences,Beijing,China
3. Genomics and Functional Proteomics Laboratories, Osteoporosis Research Center, Creighton University Medical Center,Omaha,USA
纸质出版日期:2015,
网络出版日期:2013-10-23,
Scan for full text
Zhang, Zg., Niu, Xy., Lu, Ap. et al. Effect of curcumin on aged Drosophila Melanogaster: A pathway prediction analysis., Chin. J. Integr. Med. 21, 115–122 (2015). https://doi.org/10.1007/s11655-013-1333-2
Zhi-guo Zhang, Xu-yan Niu, Ai-ping Lu, et al. Effect of curcumin on aged Drosophila Melanogaster: A pathway prediction analysis[J]. Chinese Journal of Integrative Medicine, 2015,21(2):115-122.
Zhang, Zg., Niu, Xy., Lu, Ap. et al. Effect of curcumin on aged Drosophila Melanogaster: A pathway prediction analysis., Chin. J. Integr. Med. 21, 115–122 (2015). https://doi.org/10.1007/s11655-013-1333-2 DOI:
Zhi-guo Zhang, Xu-yan Niu, Ai-ping Lu, et al. Effect of curcumin on aged Drosophila Melanogaster: A pathway prediction analysis[J]. Chinese Journal of Integrative Medicine, 2015,21(2):115-122. DOI: 10.1007/s11655-013-1333-2.
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. 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 GeneSpring 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. A total of 87 genes expressed differentially in D. melanogaster melanogaster treated with curcumin were identified
among which 50 were up-regulated significantly and 37 were remarkably down-regulated in D. melanogaster 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. Genes and their associated pathways in D. melanogaster melanogaster treated with anti-aging agent curcumin were identified using PPI network and MCODE algorithm
suggesting that curcumin may be developed as an alternative therapeutic medicine for treating aging-associated diseases.
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. 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 GeneSpring 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. A total of 87 genes expressed differentially in D. melanogaster melanogaster treated with curcumin were identified
among which 50 were up-regulated significantly and 37 were remarkably down-regulated in D. melanogaster 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. Genes and their associated pathways in D. melanogaster melanogaster treated with anti-aging agent curcumin were identified using PPI network and MCODE algorithm
suggesting that curcumin may be developed as an alternative therapeutic medicine for treating aging-associated diseases.
anti-agingCurcuminDrosophila Melanogasterpathway prediction analysisprotein-protein interaction network
anti-agingCurcuminDrosophila Melanogasterpathway prediction analysisprotein-protein interaction network
Rose MR, Burke MK, Shahrestani P, Mueller LD. Evolution of ageing since darwin. J Genet 2008;87:363–371.
Mather 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.
Romano AD, Serviddio G, de Matthaeis A, Bellanti F, Vendemiale G. Oxidative stress and aging. J Nephrol 2010;23(Suppl) 15:S29–S36.
Kang TH, Park HM, Kim YB, Kim H, Kim N, Do JH, et al. Effects of red ginseng extract on UVB irradiationinduced skin aging in hairless mice. J Ethnopharmacol 2009;123:446–451.
Brousseau 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.
Jafari M. Drosophila melanogaster as a model system for the evaluation of anti-aging compounds. Fly (Austin) 2010;4:253–257.
Lee KS, Lee BS, Semnani S, Avanesian A, Um CY, Jeon HJ, 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.
Gene 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.Nlm.Nih.Gov/geo/query/acc.Cgi?Acc=gse21182.)
Saldanha AJ. Java treeview-extensible visualization of microarray data. Bioinformatics 2004;20:3246–3248.
Real-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:S17.
Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT, Ramage D, et al. Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res 2003;13:2498–2504.
Martin A, Ochagavia ME, Rabasa LC, Miranda J, Fernandez-de-Cossio J, Bringas R. Bisogenet: a new tool for gene network building, visualization and analysis. BMC Bioinformatics 2010;11:91.
Bader GD, Hogue CW. An automated method for finding molecular complexes in large protein interaction networks. BMC Bioinformatics 2003;4:2.
Huang da W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using david bioinformatics resources. Nat Protoc 2009;4:44–57.
Ogata H, Goto S, Sato K, Fujibuchi W, Bono H, Kanehisa M. Kegg: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res 1999;27:29–34.
Thomas PD, Campbell MJ, Kejariwal A, Mi H, Karlak B, Daverman R, et al. Panther: a library of protein families and subfamilies indexed by function. Genome Res 2003;13:2129–2141.
Zhou H, Beevers CS, Huang S. The targets of curcumin. Curr Drug Targets 2011;12:332–347.
Sikora E, Bielak-Zmijewska A, Mosieniak G, Piwocka K. The promise of slow down ageing may come from curcumin. Curr Pharm Des 2010;16:884–892.
Carlson DJ, Pashaj A, Gardner K, Carlson KA. Advances in age-old questions. Fly (Austin) 2008;2:149–151.
Raman K. Construction and analysis of protein-protein interaction networks. Autom Exp 2010;2:2.
Gomez SM, Choi K, Wu Y, eds. Prediction of protein-protein interaction networks. Curr Protoc Bioinformatics 2008; John Wiley & Sons; 2008:8.2.1–8.2.14.
Carlson ME, O’Connor MS, Hsu M, Conboy IM. Notch signaling pathway and tissue engineering. Front Biosci 2007;12:5143–5156.
Presente A, Andres A, Nye JS. Requirement of notch in adulthood for neurological function and longevity. Neuroreport 2001;12:3321–3325.
Wurmbach E, Wech I, Preiss A. The enhancer of split complex of drosophila melanogaster harbors three classes of notch responsive genes. Mech Dev 1999;80:171–180.
Iso T, Kedes L, Hamamori Y. HES and HERP families: multiple effectors of the notch signaling pathway. J Cell Physiol 2003;194:237–255.
Schlatter R, Maier D. The enhancer of split and achaetescute complexes of drosophilids derived from simple urcomplexes preserved in mosquito and honeybee. BMC Evol Biol 2005;5:67.
Carlson ME, Silva HS, Conboy IM. Aging of signal transduction pathways, and pathology. Exp Cell Res 2008;314:1951–1961.
Ye X, Zerlanko B, Kennedy A, Banumathy G, Zhang R, Adams PD. Downregulation of Wnt signaling is a trigger for formation of facultative heterochromatin and onset of cell senescence in primary human cells. Mol Cell 2007;27:183–196.
Cao JN, Gollapudi S, Sharman EH, Jia Z, Gupta S. Agerelated alterations of gene expression patterns in human CD8+ T cells. Aging Cell 2010;9:19–31.
Rauner M, Sipos W, Pietschmann P. Age-dependent Wnt gene expression in bone and during the course of osteoblast differentiation. Age (Dordr) 2008;30:273–282.
Thompson B, Townsley F, Rosin-Arbesfeld R, Musisi H, Bienz M. A new nuclear component of the Wnt signalling pathway. Nat Cell Biol 2002;4:367–373.
Kramps T, Peter O, Brunner E, Nellen D, Froesch B, Chatterjee S, et al. Wnt/wingless signaling requires bcl9/legless-mediated recruitment of pygopus to the nuclear beta-catenin-tcf complex. Cell 2002;109:47–60.
Chen G, Fernandez J, Mische S, Courey AJ. A functional interaction between the histone deacetylase rpd3 and the corepressor groucho in drosophila development. Genes Dev 1999;13:2218–2230.
Ye F, Chen Y, Hoang T, Montgomery RL, Zhao XH, Bu H, et al. Hdac1 and hdac2 regulate oligodendrocyte differentiation by disrupting the beta-catenin-tcf interaction. Nat Neurosci 2009;12:829–838.
Rogina B, Helfand SL, Frankel S. Longevity regulation by drosophila rpd3 deacetylase and caloric restriction. Science 2002;298:1745.
Barker N, Hurlstone A, Musisi H, Miles A, Bienz M, Clevers H. The chromatin remodelling factor brg-1 interacts with beta-catenin to promote target gene activation. EMBO J 2001;20:4935–4943.
Park JI, Venteicher AS, Hong JY, Choi J, Jun S, Shkreli M, et al. Telomerase modulates Wnt signalling by association with target gene chromatin. Nature 2009;460:66–72.
de Boer J, Andressoo JO, de Wit J, Huijmans J, Beems RB, van Steeg H, et al. Premature aging in mice deficient in DNA repair and transcription. Science 2002;296:1276–1279.
Garinis GA, Schumacher B. Transcription-blocking DNA damage in aging and longevity. Cell Cycle 2009;8:2134–2135.
Apone LM, Virbasius CM, Reese JC, Green MR. Yeast taf(ii)90 is required for cell-cycle progression through g2/m but not for general transcription activation. Genes Dev 1996;10:2368–2380.
Kirschner DB, vom Baur E, Thibault C, Sanders SL, Gangloff YG, Davidson I, et al. Distinct mutations in yeast taf(ii)25 differentially affect the composition of tfiid and saga complexes as well as global gene expression patterns. Mol Cell Biol 2002;22:3178–3193.
Walker SS, Shen WC, Reese JC, Apone LM, Green MR. Yeast taf(ii)145 required for transcription of g1/s cyclin genes and regulated by the cellular growth state. Cell 1997;90:607–614.
Kumazaki T, Mitsui Y. Alterations in transcription factor-binding activities to fibronectin promoter during aging of vascular endothelial cells. Mech Ageing Dev 1996;88:111–124.
Makrides SC. Protein synthesis and degradation during aging and senescence. Biol Rev Camb Philos Soc 1983;58:343–422.
Shikama N, Brack C. Changes in the expression of genes involved in protein synthesis during drosophila aging. Gerontology 1996;42:123–136.
Wu M, Liu H, Fannin J, Katta A, Wang Y, Arvapalli RK, et al. Acetaminophen improves protein translational signaling in aged skeletal muscle. Rejuvenation Res 2010;13:571–579.
Andersen JB, Mazan-Mamczarz K, Zhan M, Gorospe M, Hassel BA. Ribosomal protein mrnas are primary targets of regulation in rnase-I-induced senescence. RNA Biol 2009;66:305–315.
Lachapelle S, Gagne JP, Garand C, Desbiens M, Coulombe Y, Bohr VA, et al. Proteome-wide identification of wrn-interacting proteins in untreated and nuclease-treated samples. J Proteome Res 2011;10:1216–1227.
Bauer JH, Poon PC, Glatt-Deeley H, Abrams JM, Helfand SL. Neuronal expression of p53 dominant-negative proteins in adult drosophila melanogaster extends life span. Curr Biol 2005;15:2063–2068.
Stommel JM, Wahl GM. A new twist in the feedback loop: stress-activated mdm2 destabilization is required for p53 activation. Cell Cycle 2005;4:411–417.
Hunziker A, Jensen MH, Krishna S. Stress-specific response of the p53-mdm2 feedback loop. BMC Syst Biol 2010;4:94.
Zhang T, Prives C. Cyclin a-cdk phosphorylation regulates mdm2 protein interactions. J Biol Chem 2001;276:29702–29710.
Wang Z, Qi Y, Chen Q, Yang D, Tang S, Jin X, et al. Cyclin a is essential for the p53-modulated inhibition from benzo(a)pyrene toxicity in a549 cells. Toxicology 2009;256:1–6.
Pajalunga D, Crescenzi M. Regulation of cyclin e protein levels through e2f-mediated inhibition of degradation. Cell Cycle 2004;3:1572–1578.
Barton MC, Akli S, Keyomarsi K. Deregulation of cyclin e meets dysfunction in p53: closing the escape hatch on breast cancer. J Cell Physiol 2006;209:686–694.
Sherr CJ. Tumor surveillance via the arf-p53 pathway. Genes Dev 1998;12:2984–2991.
Furukawa Y, Nishimura N, Satoh M, Endo H, Iwase S, Yamada H, et al. Apaf-1 is a mediator of e2f-1-induced apoptosis. J Biol Chem 2002;277:39760–39768.
Luo J, Su F, Chen D, Shiloh A, Gu W. Deacetylation of p53 modulates its effect on cell growth and apoptosis. Nature 2000;408:377–381.
Kim MM, Yoon SO, Cho YS, Chung AS. Histone deacetylases, hdac1 and hsir2, act as a negative regulator of ageing through p53 in human gingival fibroblast. Mech Ageing Dev 2004;125:351–357.
Gupta SC, Prasad S, Kim JH, Patchva S, Webb LJ, Priyadarsini IK, et al. Multitargeting by curcumin as revealed by molecular interaction studies. Nat Prod Rep 2011;28:1937–1955.
0
浏览量
51
Downloads
2
CSCD
关联资源
相关文章
相关作者
相关机构