| Literature DB >> 32649993 |
Takeshi Terabayashi1, Gregory G Germino1, Luis F Menezes2.
Abstract
Systems-based, agnostic approaches focusing on transcriptomics data have been employed to understand the pathogenesis of polycystic kidney diseases (PKD). While multiple signaling pathways, including Wnt, mTOR and G-protein-coupled receptors, have been implicated in late stages of disease, there were few insights into the transcriptional cascade immediately downstream of Pkd1 inactivation. One of the consistent findings has been transcriptional evidence of dysregulated metabolic and cytoskeleton remodeling pathways. Recent technical developments, including bulk and single-cell RNA sequencing technologies and spatial transcriptomics, offer new angles to investigate PKD. In this article, we review what has been learned based on transcriptional approaches and consider future opportunities. Published by Elsevier Inc.Entities:
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Year: 2020 PMID: 32649993 PMCID: PMC9447370 DOI: 10.1016/j.cellsig.2020.109701
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.850