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Identification of modules related to programmed cell death in CHD based on EHEN

  • Xu Jia
  • , Wan Li
  • , Zhengqiang Miao
  • , Chenchen Feng
  • , Zhe Liu
  • , Yuehan He
  • , Junjie Lv
  • , Youwen Du
  • , Min Hou
  • , Weiming He*
  • , Danbin Li
  • , Lina Chen*
  • *Corresponding author for this work

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

45 Downloads (CityUHK Scholars)

Abstract

The formation and death of macrophages and foam cells are one of the major factors that cause coronary heart disease (CHD). In our study, based on the Edinburgh Human Metabolic Network (EHMN) metabolic network, we built an enzyme network which was constructed by enzymes (nodes) and reactions (edges) called the Edinburgh Human Enzyme Network (EHEN). By integrating the subcellular location information for the reactions and refining the protein-reaction relationships based on the location information, we proposed a computational approach to select modules related to programmed cell death. The identified module was in the EHEN-mitochondria (EHEN-M) and was confirmed to be related to programmed cell death, CHD pathogenesis, and lipid metabolism in the literature. We expected this method could analyze CHD better and more comprehensively from the point of programmed cell death in subnetworks.
Original languageEnglish
Article number475379
JournalBioMed Research International
Volume2014
Online published15 Jul 2014
DOIs
Publication statusPublished - 2014
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Publisher's Copyright Statement

  • This full text is made available under CC-BY 3.0. https://creativecommons.org/licenses/by/3.0/

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