Mesalamine modulates intercellular adhesion intercellular adhesion through inhibition of p-21 activated kinase-1
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F13%3A00067648" target="_blank" >RIV/00216224:14740/13:00067648 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1016/j.bcp.2012.10.026" target="_blank" >http://dx.doi.org/10.1016/j.bcp.2012.10.026</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.bcp.2012.10.026" target="_blank" >10.1016/j.bcp.2012.10.026</a>
Alternative languages
Result language
angličtina
Original language name
Mesalamine modulates intercellular adhesion intercellular adhesion through inhibition of p-21 activated kinase-1
Original language description
Mesalamine (5-ASA) is widely used for the treatment of ulcerative colitis, a remitting condition characterized by chronic inflammation of the colon. Knowledge about the molecular and cellular targets of 5-ASA is limited and a clear understanding of its activity in intestinal homeostasis and interference with neoplastic progression is lacking. We sought to identify molecular pathways interfered by 5-ASA, using CRC cell lines with different genetic background. Microarray was performed for gene expressionprofile of 5-ASA-treated and untreated cells (HCT116 and HT29). Filtering and analysis of data identified three oncogenic pathways interfered by 5-ASA: MAPK/ERK pathway, cell adhesion and beta-catenin/Wnt signaling. PAK1 emerged as a consensus target of5-ASA, orchestrating these pathways. We further investigated the effect of 5-ASA on cell adhesion. 5-ASA increased cell adhesion which was measured by cell adhesion assay and transcellular-resistance measurement.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
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Continuities
O - Projekt operacniho programu
Others
Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Biochemical Pharmacology
ISSN
0006-2952
e-ISSN
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Volume of the periodical
85
Issue of the periodical within the volume
2
Country of publishing house
GB - UNITED KINGDOM
Number of pages
11
Pages from-to
234-244
UT code for WoS article
000314143400011
EID of the result in the Scopus database
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