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CN 34-1304/RISSN 1674-3679

Volume 24 Issue 3
Jun.  2020
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WANG Hui-hui, SA Jian, CAO Hong-yan, CUI Yue-hua. Difference analysis of myeloid leukemia fusion oncogene expression network based on time series[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2020, 24(3): 274-278. doi: 10.16462/j.cnki.zhjbkz.2020.03.006
Citation: WANG Hui-hui, SA Jian, CAO Hong-yan, CUI Yue-hua. Difference analysis of myeloid leukemia fusion oncogene expression network based on time series[J]. CHINESE JOURNAL OF DISEASE CONTROL & PREVENTION, 2020, 24(3): 274-278. doi: 10.16462/j.cnki.zhjbkz.2020.03.006

Difference analysis of myeloid leukemia fusion oncogene expression network based on time series

doi: 10.16462/j.cnki.zhjbkz.2020.03.006
Funds:  National Natural Science Foundation of China(71403156); Shanxi Scholarship Council of China(2017-054); Applied Basic Research Program of Shanxi Province(201901D111204)
More Information
  • Corresponding author: CAO Hong-yan,E-mail:cao_hong_yan@163.com; CUI Yue-hua,E-mail:cui@stt.msu.edu
  • Received Date: 2019-09-30
  • Rev Recd Date: 2019-12-20
  • Publish Date: 2020-03-10
  •   Objective   Focusing on four types acute myeloid leukemia(AML)fusion oncogenes, so as to explore the network difference with time series expression data and further identify important genes in networks.   Methods   Gene network difference analysis was conducted while focusing on the global attributes of the union network. The CompNet neighborhood similarity index(CNSI) was adopted to assess network similarity. "fast-greedy" algorithm was used to detect communities based on the union network, and further identify hub genes.   Results   The CNSI value between NUP98-HOXA9-3 d and NUP98-HOXA9-8 d was 0.73, while AML1-ETO-6 h and PML-RARA-6 h was 0.25. We identified ten AML associated genes and seven of them(TNF, VEGFA, EP300, EGF, CD44, PTGS2, SMAD3) were reported in the literature.   Conclusions   The network difference analysis revealed the pattern and heterogeneity of AML gene expression change across different time points, and further provided target genes for efficient treatment of AML with different types of fusion oncogenes.
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