Title |
Microarray Integrated Analysis of a Gene Network for the CD36 Myocardial Phenotype
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Authors |
Imane Sabaouni1,*, Brigitte Vannier2, Ahmed Moussa3 & Azeddine Ibrahimi1
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Affiliation |
1Medical Biotechnology Lab (MedBiotech), Rabat Medical & Pharmacy School, Mohammed Vth University in Rabat, Morocco; 2Receptors, Regulation and Tumor Cells (2RTC) Laboratory, University of Poitiers, France; 3LabTIC Laboratory, ENSA, Abdelmalek Essaadi University, Tangier, Morocco
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Imane SABAOUNI – E-mail: imanesabaouni@yahoo.com *Corresponding author
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Article Type |
Hypothesis
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Date |
Received July 18, 2016; Revised July 29, 2016; Accepted July 30, 2016; Published October 11, 2016
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Abstract |
CD36 is a multifunctional
membrane-type receptor glycoprotein that reacts with oxidized
low-density lipoprotein and long-chain fatty acid (LCFA). However,
much remains to be understood about the molecular mechanism of the
cardio-myopathy observed in CD36-KO mice. In this study, we identify
different genes pathways involved in response to CD36 cardio-myopathy
phenotype by identifying the differences among biological processes,
molecular pathways and networks of interactions that emerge from
knocking CD3 and using different bioinformatics tools such as
STRING, GeneMANIA and Cytoscape. We were able list all the
CD36-regulated genes, their related function and their specific
networks. Data analysis showed that CD36-regulated genes
differentially expressed are involved in
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Keywords |
CD36, cardio-myopathy, genes networks, genes pathways, metabolism, angiogenesis/apoptosis.
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Citation |
Sabaouni et al. Bioinformation 12(6): 332-339 (2016)
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Edited by |
P Kangueane
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ISSN |
0973-2063
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Publisher |
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License |
This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.
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