AI Article Synopsis

  • The COP9 signalosome, which plays a role in cancer genetics through its deneddylase activity, shows a complicated expression pattern in normal tissues that differs in tumors.
  • Seven COP9 genes were found to express synergistically in normal head and neck tissues, while this expression coordination decreased in tumors.
  • The study highlights a strong link between COP9 gene expressions and mitochondrial function, suggesting the value of TCGA data for understanding both normal cell physiology and cancer biology.

Article Abstract

Background: The COP9 signalosome, composed of eight subunits, is implicated in cancer genetics with its deneddylase activity to modulate cellular concentration of oncogenic proteins such as IkB and TGFβ. However, its function in the normal cell physiology remains elusive. Primarily focusing on gene expression data of the normal tissues of the head and neck, the cancer genome atlas (TCGA) database was used to identify groups of genes that were expressed synergistically with the COP9 genes, particularly with the COPS5 (CSN5), which possesses the catalytic activity of COP9.

Results: Expressions of seven of the COP9 genes (COPS2, COPS3, COPS4, COPS5, COPS6, COPS7A, and COPS8) were found to be highly synergistic in the normal tissues. In contrast, the tumor tissues decreased the coordinated expression pattern of COP9 genes. Pathway analysis revealed a high coordination of the expression of the COPS5 and the other COP9 genes with mitochondria-related functional pathways, including genes encoding the respiratory chain complex.

Conclusions: The results indicate that mRNA expression data for the matched normal tissues available in TCGA are statistically reliable, and are highly useful to assess novel associations of genes with functional pathways in normal physiology as well as in the cancer tissues. This study revealed the significant correlation between the expressions of the COP9 genes and those related to the mitochondrial activity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131501PMC
http://dx.doi.org/10.1186/s12864-016-3313-yDOI Listing

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