Literature DB >> 12644633

Gene expression profiling of Caco-2 BBe cells suggests a role for specific signaling pathways during intestinal differentiation.

James C Fleet1, Liyong Wang, Olga Vitek, Bruce A Craig, Howard J Edenberg.   

Abstract

We examined the pattern of gene expression resulting from spontaneous differentiation of Caco-2 BBe cells to gain insight into the molecular changes necessary for enterocyte differentiation. RNA was prepared from cells harvested at three cell stages: proliferating (50% confluent, 2 days in culture), postproliferative nondifferentiated (8 days), and differentiated (15 days). Gene expression profiles were determined using Affymetrix Human Genome U95A GeneChips. Differentially expressed genes were identified following statistical analysis (i.e., ANOVA, bootstrapping adjustments to P values, false detection rate criterion). We identified 1,150 unique genes as differentially expressed; expression of 48.6% fell and 46% increased from 2 to 15 days, while 5.4% had expression that either peaked or dipped at 8 days. Genes expressed during differentiation included several small-intestine-specific genes involved in nutrient transport/metabolism, e.g., DCT1, hephaestin, folate receptor 1, sucrase-isomaltase, and apolipoproteins CI, CIII, B100, H, and M, indicating that this colonic adenocarcinoma cell line has a hybrid colonocyte/enterocyte phenotype. Patterns of gene expression based upon functional classification suggest a role for cell-cell/cell-matrix interactions, suppression of Wnt signaling, and activation of TGFbeta and phosphatidylinositol 3-kinase pathways during enterocyte differentiation.

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Year:  2003        PMID: 12644633     DOI: 10.1152/physiolgenomics.00152.2002

Source DB:  PubMed          Journal:  Physiol Genomics        ISSN: 1094-8341            Impact factor:   3.107


  26 in total

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Authors:  Michael P Verzi; Hyunjin Shin; H Hansen He; Rita Sulahian; Clifford A Meyer; Robert K Montgomery; James C Fleet; Myles Brown; X Shirley Liu; Ramesh A Shivdasani
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2.  Transporter and ion channel gene expression after Caco-2 cell differentiation using 2 different microarray technologies.

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Journal:  J Steroid Biochem Mol Biol       Date:  2013-10-28       Impact factor: 4.292

Review 5.  Intestinal epithelial cells in vitro.

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7.  Mybl2, downregulated during colon epithelial cell maturation, is suppressed by miR-365.

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Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2011-07-07       Impact factor: 4.052

8.  In vitro treatment of carcinoma cell lines with pancreatic (pro)enzymes suppresses the EMT programme and promotes cell differentiation.

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9.  Global gene expression analysis in time series following N-acetyl L-cysteine induced epithelial differentiation of human normal and cancer cells in vitro.

Authors:  Anna C Gustafsson; Ilya Kupershmidt; Esther Edlundh-Rose; Giulia Greco; Annalucia Serafino; Eva K Krasnowska; Thomas Lundeberg; Luisa Bracci-Laudiero; Maria-Concetta Romano; Tiziana Parasassi; Joakim Lundeberg
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10.  Proteomic changes during intestinal cell maturation in vivo.

Authors:  Jinsook Chang; Mark R Chance; Courtney Nicholas; Naseem Ahmed; Sandra Guilmeau; Marta Flandez; Donghai Wang; Do-Sun Byun; Shannon Nasser; Joseph M Albanese; Georgia A Corner; Barbara G Heerdt; Andrew J Wilson; Leonard H Augenlicht; John M Mariadason
Journal:  J Proteomics       Date:  2008-09-12       Impact factor: 4.044

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