Comparative gene expression analysis in mouse models for identifying critical pathways in mammary gland development

被引:8
作者
Zhao, Hongbo [2 ]
Huang, Mini [1 ]
Chen, Qiang [1 ,3 ]
Wang, Qishan [1 ,3 ]
Pan, Yuchun [1 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Agr & Biol, Shanghai 200240, Peoples R China
[2] Kunming Med Coll, Inst Mol & Clin Med, Kunming 650500, Peoples R China
[3] Shanghai Key Lab Anim Biotechnol, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Mammary gland; Microarray; Gene set enrichment analysis; Pathways; BREAST-CANCER; EPITHELIAL-CELLS; PROBE LEVEL; INVOLUTION; ACTIVATION; LACTATION; INDUCTION; PREGNANCY; ROLES; ATLAS;
D O I
10.1007/s10549-011-1650-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Functional development of the mammary gland is an important physiological process. Several studies have used gene expression profiling of mammary gland development to identify the key genes in the process, but few focused on the involved pathways. And there is a lack of concordance between those observed pathways. In this article, we applied a standardized microarray preprocessing to four independent studies, and then used gene set enrichment analysis (GSEA) to identify the key pathways. The result demonstrated an increased concordance between these expression profiling data sets. From the stage of puberty to pregnancy, we found 7 up-regulated and 6 down-regulated pathways in common. From the period of pregnancy to lactation, we found 7 up-regulated and 58 down-regulated pathways in common. And 10 up-regulated and 3 down-regulated pathways were found in common from lactation to the involution period. The main canonical pathways identified belong to immune system, cell communication, metabolism, and disease-related pathways. Pathway analysis is a more effective method than single gene analysis because the former one can able to detect genes weakly connected to the phenotype. As we applied GSEA to the study, our findings suggested a greater concordance in this physiological process. The critical pathways we find can provide some insight of functional development of the mammary gland and motivate other relative studies.
引用
收藏
页码:969 / 977
页数:9
相关论文
共 34 条
[1]   Key stages in mammary gland development - Secretory activation in the mammary gland: it's not just about milk protein synthesis! [J].
Anderson, Steven M. ;
Rudolph, Michael C. ;
McManaman, James L. ;
Neville, Margaret C. .
BREAST CANCER RESEARCH, 2007, 9 (01)
[2]   TRANSFORMING GROWTH-FACTOR-BETA ACTIVATION IN IRRADIATED MARINE MAMMARY-GLAND [J].
BARCELLOSHOFF, MH ;
DERYNCK, R ;
TSANG, MLS ;
WEATHERBEE, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (02) :892-899
[3]  
BUSE P, 1995, J BIOL CHEM, V270, P28223
[4]   NF-κB in mammary gland development and breast cancer [J].
Cao, YX ;
Karin, M .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 2003, 8 (02) :215-223
[5]   Gene expression profiling of mammary gland development reveals putative roles for death receptors and immune mediators in post-lactational regression [J].
Clarkson, RWE ;
Wayland, MT ;
Lee, J ;
Freeman, T ;
Watson, CJ .
BREAST CANCER RESEARCH, 2004, 6 (02) :R92-R109
[6]   affy -: analysis of Affymetrix GeneChip data at the probe level [J].
Gautier, L ;
Cope, L ;
Bolstad, BM ;
Irizarry, RA .
BIOINFORMATICS, 2004, 20 (03) :307-315
[7]  
Gentleman R, 2011, USING CATEGORIES ANA
[8]   Bioconductor: open software development for computational biology and bioinformatics [J].
Gentleman, RC ;
Carey, VJ ;
Bates, DM ;
Bolstad, B ;
Dettling, M ;
Dudoit, S ;
Ellis, B ;
Gautier, L ;
Ge, YC ;
Gentry, J ;
Hornik, K ;
Hothorn, T ;
Huber, W ;
Iacus, S ;
Irizarry, R ;
Leisch, F ;
Li, C ;
Maechler, M ;
Rossini, AJ ;
Sawitzki, G ;
Smith, C ;
Smyth, G ;
Tierney, L ;
Yang, JYH ;
Zhang, JH .
GENOME BIOLOGY, 2004, 5 (10)
[9]   Exploration, normalization, and summaries of high density oligonucleotide array probe level data [J].
Irizarry, RA ;
Hobbs, B ;
Collin, F ;
Beazer-Barclay, YD ;
Antonellis, KJ ;
Scherf, U ;
Speed, TP .
BIOSTATISTICS, 2003, 4 (02) :249-264
[10]  
Li ML, 1996, CELL GROWTH DIFFER, V7, P3