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MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms.

MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms. Research Abstract Details 

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  • MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms. Abstract Text:

    a p singhA P Singh,s c chauhanS C Chauhan,m andrianifahananaM Andrianifahanana,n moniauxN Moniaux,j l mezaJ L Meza,m c copinM C Copin,i van seuningenI van Seuningen,m a hollingsworthM A Hollingsworth,j p aubertJ P Aubert,s k batraS K Batra,

    MUC4 mucin is a high molecular weight transmembrane glycoprotein that plays important roles in tumour biology. It is aberrantly expressed in pancreatic adenocarcinoma, while not being detectable in the normal pancreas. Previous studies have demonstrated that the cystic fibrosis transmembrane conductance regulator (CFTR), a chloride channel that is defective in CF, is implicated in multiple cellular functions, including gene regulation. In the present study, using a CFTR-defective pancreatic cancer cell line and its derived subline expressing functional CFTR, we report that MUC4 expression is negatively regulated by CFTR. Short-interfering RNA (siRNA)-mediated silencing of CFTR also leads to an increased expression of MUC4. Additionally, our results suggest that CFTR-mediated regulation of MUC4 is cell density-dependent and is achieved by transcriptional and posttranslational mechanisms. Moreover, in a panel of pancreatic cancer cell lines and normal pancreas, we observed that CFTR was downregulated in pancreatic cancer cells and negatively correlated with MUC4 in most cases. An aberrant expression of MUC4 was also detected in the CF pancreas. Downregulation of CFTR in pancreatic adenocarcinoma and its inverse association with the tumour-linked mucin, MUC4, indicate novel function(s) of CFTR in pancreatic tumour biology and suggest the implication of new signalling pathway(s) in MUC4 regulation.

    MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms. Publishing Authors By Initials

    ap singhAP Singh,sc chauhanSC Chauhan,m andrianifahananaM Andrianifahanana,n moniauxN Moniaux,jl mezaJL Meza,mc copinMC Copin,i van seuningenI van Seuningen,ma hollingsworthMA Hollingsworth,jp aubertJP Aubert,sk batraSK Batra,

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    PUBMED ID PMID:

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    MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Oncogene

    VOLUME: 26

    Page Numbers: 30-41

    Journal Abbreviation: Oncogene

    ISSN: 0950-9232

    DAY: 26

    MONTH: 06

    YEAR: 2006

    MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8711562

    MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms. Keywords Mesh Terms:

    KEYWORDS: Reverse Transcriptase Polymerase Chain R

    MESH TERMS: genetics

    Chemical & Substance for Abstract: MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms. Information

    Substance Name: Cystic Fibrosis Transmembrane Conductanc

    Registry Number: 126880-72-6

    Grant and Affiliation Information for MUC4 expression is regulated by cystic fibrosis transmembrane conductance regulator in pancreatic adenocarcinoma cells via transcriptional and post-translational mechanisms.

    AFFILIATION: Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, NE 68198-5870, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NCI

    GRANT: R01 CA78590

    ACRONYM: CA

    MEDLINETA: Oncogene

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