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pmid:26217796

Data supporting the identification of compound for inhibition of survivin of colorectal cancer by using ingenuity pathway analysis of gene expression profiling of colorectal cancer tissues.

Yi-Chao Lee · Jun-Wei Lee · Chi-Chen Huang · Ming-Heng Wu · Kuen-Haur Lee

Data in brief · 2015 doi:10.1016/j.dib.2015.05.017

Paper

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Experiment

complete

Data

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Execution

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title
Data supporting the identification of compound for inhibition of survivin of colorectal cancer by using ingenuity pathway analysis of gene expression profiling of colorectal cancer tissues.
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10.1016/j.dib.2015.05.017
pmid
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Yi-Chao Lee
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Jun-Wei Lee
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Chi-Chen Huang
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Ming-Heng Wu
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Kuen-Haur Lee
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year
2015
abstract
The data in this article is related to the research article entitled, "Targeting of Multiple Oncogenic Signaling Pathways by Hsp90 Inhibitor Alone or in Combination with Berberine for Treatment of Colorectal Cancer" [1]. Overexpression of survivin induces resistance to various anticancer therapies such as chemotherapy and radiation therapy in colorectal cancer (CRC) cells. To determine significant correlations of biological functions/pathways with survivin, 4567 significant genes were analyzed from the GEO DataSet (GSE21815) of CRC and these were overlaid onto a global molecular network developed from information contained in the Ingenuity Pathway Analysis (IPA) database. The data here present the most significant disease and disordered biological functions, significant molecular/cellular functions and significant categories in physiological development/system functions which were associated with CRC. The top 10 canonical signaling pathways associated with CRC were categorize in order based on the level of statistical significance.
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