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Generalized Portrait of Cancer Metabolic Pathways Inferred from a List of Genes Overexpressed in Cancer
Author(s) -
Eugenia Poliakov,
David Managadze,
Igor B. Rogozin
Publication year - 2014
Publication title -
genetics research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.351
H-Index - 9
eISSN - 2090-3154
pISSN - 2090-3162
DOI - 10.1155/2014/646193
Subject(s) - cancer , cancer cell , biology , gene , warburg effect , carcinogenesis , metabolic pathway , kegg , cancer research , glycolysis , transcriptome , computational biology , genetics , enzyme , gene expression , biochemistry
More than half a century from postulated Warburg theory of cancer cells origin, a question of changed metabolism in cancer is again taking the central place. Generalized picture of cancer metabolism was replaced by analysis of signaling and oncogenes in each type of cancer for several decades. However, now empowered with wealth of knowledge about tumor suppressors, oncogenes, and signaling pathways, reprogramming of cellular metabolism (e.g., increased glycolysis to respiration ratio in cancer cells) reemerged as an important element of cancer progression. To analyze level of expression of various proteins including metabolic enzymes across various cancers we used dbEST and Unigene data. We delineated a list of genes that are overexpressed in different types of cancer. We also grouped overexpressed enzymes into KEGG pathways and analyzed adjacent pathways to describe enzymatic reactions that take place in cancer cells and to identify major players that are abundant in cancer protein machinery. Glycolysis/gluconeogenesis and oxidative phosphorylation are the most abundant pathways although several other pathways are enriched in genes from our list. Ubiquitously overexpressed genes could be marked as nonspecific cancer-associated genes when analyzing genes that are overexpressed in certain types of cancer. Thus the list of overexpressed genes may be a useful tool for cancer research.

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