Literature DB >> 18464289

Insig2 is associated with colon tumorigenesis and inhibits Bax-mediated apoptosis.

Chang Gong Li1, Mike Gruidl1, Steven Eschrich1, Susan McCarthy1, Hong-Gang Wang1, Mark G Alexandrow1, Timothy J Yeatman1.   

Abstract

Insulin-induced gene 2 (Insig2) was recently identified as a putative positive prognostic biomarker for colon cancer prognosis. Insig2 has been previously reported to be an endoplasmic reticulum (ER) membrane protein, and a negative regulator of cholesterol synthesis. Here we report that Insig2 was validated as a gene with univariate negative prognostic capacity to discriminate human colon cancer survivorship. To investigate the functional roles it plays in tumor development and malignancy, Insig2 was over-expressed in colon cancer cells resulting in increased cellular proliferation, invasion, anchorage independent growth and inhibition of apoptosis. Over-expression of Insig2 appeared to suppress chemotherapeutic drug treatment-induced Bcl2 associated X protein (Bax) expression and activation. Insig2 was also found to localize to the mitochondria/heavy membrane fraction and associate with conformationally changed Bax. Moreover, Insig2 altered the expression of several additional apoptosis genes located in mitochondria, further supporting its new functional role in regulating mitochondrial mediated apoptosis. Our findings show that Insig2 is a novel colon cancer biomarker, and suggest, for the first time, a reasonable connection between Insig2 and Bax-mediated apoptosis through the mitochondrial pathway. (c) 2008 Wiley-Liss, Inc.

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Year:  2008        PMID: 18464289      PMCID: PMC2650850          DOI: 10.1002/ijc.23510

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  47 in total

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Authors:  B E Kreger; K M Anderson; A Schatzkin; G L Splansky
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8.  Molecular cloning and in situ localization of the human contactin gene (CNTN1) on chromosome 12q11-q12.

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Journal:  Genomics       Date:  1994-06       Impact factor: 5.736

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Authors:  K G Wolter; Y T Hsu; C L Smith; A Nechushtan; X G Xi; R J Youle
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5.  Whole blood transcriptomics and urinary metabolomics to define adaptive biochemical pathways of high-intensity exercise in 50-60 year old masters athletes.

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