Novel structural co-expression analysis linking the NPM1-associated ribosomal biogenesis network to chronic myelogenous leukemia
Author(s) -
Lawrence Chan,
Xihong Lin,
Godwin Yung,
Thomas Ka-Luen Lui,
Ya Ming Chiu,
Fengfeng Wang,
Nancy B. Y. Tsui,
William C. Cho,
Shea Ping Yip,
Parco M. Siu,
Sze Chuen Cesar Wong,
Benjamin YatMing Yung
Publication year - 2015
Publication title -
scientific reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.24
H-Index - 213
ISSN - 2045-2322
DOI - 10.1038/srep10973
Subject(s) - npm1 , chronic myelogenous leukemia , ribosome biogenesis , biology , computational biology , breakpoint cluster region , transcriptome , gene expression , cancer research , nucleophosmin , gene , genetics , leukemia , ribosome , rna , karyotype , chromosome
Co-expression analysis reveals useful dysregulation patterns of gene cooperativeness for understanding cancer biology and identifying new targets for treatment. We developed a structural strategy to identify co-expressed gene networks that are important for chronic myelogenous leukemia (CML). This strategy compared the distributions of expressional correlations between CML and normal states, and it identified a data-driven threshold to classify strongly co-expressed networks that had the best coherence with CML. Using this strategy, we found a transcriptome-wide reduction of co-expression connectivity in CML, reflecting potentially loosened molecular regulation. Conversely, when we focused on nucleophosmin 1 ( NPM1 ) associated networks, NPM1 established more co-expression linkages with BCR-ABL pathways and ribosomal protein networks in CML than normal. This finding implicates a new role of NPM1 in conveying tumorigenic signals from the BCR-ABL oncoprotein to ribosome biogenesis, affecting cellular growth. Transcription factors may be regulators of the differential co-expression patterns between CML and normal.
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