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- Publisher Website: 10.1091/mbc.E07-04-0309
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- PMID: 17699589
- WOS: WOS:000250740000005
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Article: Parallels between global transcriptional programs of polarizing Caco-2 intestinal epithelial cells in vitro and gene expression programs in normal colon and colon cancer
Title | Parallels between global transcriptional programs of polarizing Caco-2 intestinal epithelial cells in vitro and gene expression programs in normal colon and colon cancer |
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Authors | |
Issue Date | 2007 |
Publisher | American Society for Cell Biology. The Journal's web site is located at http://www.molbiolcell.org/ |
Citation | Molecular Biology of the Cell, 2007, v. 18 n. 11, p. 4245-4260 How to Cite? |
Abstract | Posttranslational mechanisms are implicated in the development of epithelial cell polarity, but little is known about the patterns of gene expression and transcriptional regulation during this process. We characterized temporal patterns of gene expression during cell-cell adhesion-initiated polarization of cultured human Caco-2 cells, which develop structural and functional polarity resembling enterocytes in vivo. A distinctive switch in gene expression patterns occurred upon formation of cell-cell contacts. Comparison to gene expression patterns in normal human colon and colon tumors revealed that the pattern in proliferating, nonpolarized Caco-2 cells paralleled patterns seen in human colon cancer in vivo, including expression of genes involved in cell proliferation. The pattern switched in polarized Caco-2 cells to one more closely resembling that in normal colon tissue, indicating that regulation of transcription underlying Caco-2 cell polarization is similar to that during enterocyte differentiation in vivo. Surprisingly, the temporal program of gene expression in polarizing Caco-2 cells involved changes in signaling pathways (e.g., Wnt, Hh, BMP, FGF) in patterns similar to those during migration and differentiation of intestinal epithelial cells in vivo, despite the absence of morphogen gradients and interactions with stromal cells characteristic of enterocyte differentiation in situ. The full data set is available at http://microarray-pubs.stanford.edu/CACO2. © 2007 by The American Society for Cell Biology. |
Persistent Identifier | http://hdl.handle.net/10722/57152 |
ISSN | 2023 Impact Factor: 3.1 2023 SCImago Journal Rankings: 1.566 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Sääf, AM | en_HK |
dc.contributor.author | Halbleib, JM | en_HK |
dc.contributor.author | Chen, X | en_HK |
dc.contributor.author | Siu, TY | en_HK |
dc.contributor.author | Suet, YL | en_HK |
dc.contributor.author | Nelson, WJ | en_HK |
dc.contributor.author | Brown, PO | en_HK |
dc.date.accessioned | 2010-04-12T01:27:26Z | - |
dc.date.available | 2010-04-12T01:27:26Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Molecular Biology of the Cell, 2007, v. 18 n. 11, p. 4245-4260 | en_HK |
dc.identifier.issn | 1059-1524 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/57152 | - |
dc.description.abstract | Posttranslational mechanisms are implicated in the development of epithelial cell polarity, but little is known about the patterns of gene expression and transcriptional regulation during this process. We characterized temporal patterns of gene expression during cell-cell adhesion-initiated polarization of cultured human Caco-2 cells, which develop structural and functional polarity resembling enterocytes in vivo. A distinctive switch in gene expression patterns occurred upon formation of cell-cell contacts. Comparison to gene expression patterns in normal human colon and colon tumors revealed that the pattern in proliferating, nonpolarized Caco-2 cells paralleled patterns seen in human colon cancer in vivo, including expression of genes involved in cell proliferation. The pattern switched in polarized Caco-2 cells to one more closely resembling that in normal colon tissue, indicating that regulation of transcription underlying Caco-2 cell polarization is similar to that during enterocyte differentiation in vivo. Surprisingly, the temporal program of gene expression in polarizing Caco-2 cells involved changes in signaling pathways (e.g., Wnt, Hh, BMP, FGF) in patterns similar to those during migration and differentiation of intestinal epithelial cells in vivo, despite the absence of morphogen gradients and interactions with stromal cells characteristic of enterocyte differentiation in situ. The full data set is available at http://microarray-pubs.stanford.edu/CACO2. © 2007 by The American Society for Cell Biology. | en_HK |
dc.language | eng | en_HK |
dc.publisher | American Society for Cell Biology. The Journal's web site is located at http://www.molbiolcell.org/ | en_HK |
dc.relation.ispartof | Molecular Biology of the Cell | en_HK |
dc.rights | © 2007 by The American Society for Cell Biology. This article is available online at https://doi.org/10.1091/mbc.e07-04-0309. | en_HK |
dc.subject.mesh | Cell Polarity - genetics | en_HK |
dc.subject.mesh | Colon - drug effects - metabolism | en_HK |
dc.subject.mesh | Colonic Neoplasms - genetics - metabolism - pathology | en_HK |
dc.subject.mesh | Gene Expression Regulation - drug effects - genetics | en_HK |
dc.subject.mesh | Health | en_HK |
dc.title | Parallels between global transcriptional programs of polarizing Caco-2 intestinal epithelial cells in vitro and gene expression programs in normal colon and colon cancer | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Suet, YL:suetyi@hkucc.hku.hk | en_HK |
dc.identifier.authority | Suet, YL=rp00359 | en_HK |
dc.description.nature | published_or_final_version | en_HK |
dc.identifier.doi | 10.1091/mbc.E07-04-0309 | en_HK |
dc.identifier.pmid | 17699589 | - |
dc.identifier.pmcid | PMC2043540 | en_HK |
dc.identifier.scopus | eid_2-s2.0-35848935648 | en_HK |
dc.identifier.hkuros | 138951 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-35848935648&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 18 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 4245 | en_HK |
dc.identifier.epage | 4260 | en_HK |
dc.identifier.isi | WOS:000250740000005 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.citeulike | 1726480 | - |
dc.identifier.issnl | 1059-1524 | - |