Published March 30, 2017 | Version v1
Dataset Open

R-code for: A systems level analysis of epileptogenesis-associated proteome alterations

  • 1. Bioinformatics Core, Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, 4367 Belvaux, Luxembourg
  • 2. Institute of Pharmacology, Toxicology and Pharmacy, Ludwig-Maximilians-University (LMU) 80539 Munich, Germany
  • 3. Institute of Animal Physiology, Department of Veterinary Sciences, Ludwig-Maximilians-University (LMU), 80539 Munich, Germany; Experimental Ophthalmology, Philipps University of Marburg, 35037 Marburg, Germany
  • 4. Research Unit Protein Science, Helmholtz Center Munich, 85764 Neuherberg, Germany

Description

Despite intense research efforts, the knowledge about the mechanisms of epileptogenesis and epilepsy is still considered incomplete and limited. However, an in-depth understanding of molecular pathophysiological processes is crucial for the rational selection of innovative biomarkers and target candidates.

Here, we subjected proteomic data from different phases of a chronic rat epileptogenesis model to a comprehensive systems level analysis. Weighted Gene Co-expression Network analysis identified several modules of interconnected protein groups reflecting distinct molecular aspects of epileptogenesis in the hippocampus and the parahippocampal cortex. Characterization of these modules did not only further validate the data but also revealed regulation of molecular processes not described previously in the context of epilepsy development. The data sets also provide valuable information about temporal patterns, which should be taken into account for development of preventive strategies in particular when it comes to multi-targeting network pharmacology approaches.

In addition, principal component analysis suggests candidate biomarkers, which might inform the design of novel molecular imaging approaches aiming to predict epileptogenesis during different phases or confirm epilepsy manifestation. Further studies are necessary to distinguish between molecular alterations, which correlate with epileptogenesis versus those reflecting a mere consequence of the status epilepticus.

Notes

For code-related questions, please contact Ganna Androsova via ganna.androsova@uni.lu.

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