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. 2020 Feb 20;34:101460. doi: 10.1016/j.redox.2020.101460

Table 4d.

Proinflammatory and profibrotic molecules, pathways and transcription factors played important roles in pathophysiological process of ESRD.

Method Table/Figure Result
IPA Fig. 2B upregulated SGs in ESRD can active proinflammatory pathways such as IL8 signaling, neuroinflammation signaling pathway.
IPA Fig. 2D downregulated SGs in ESRD can active profibrotic pathways such as inhibition of matrix metalloporteases
TRANSFAC Table 3C upregulated SGs in ESRD may be modulated by transcription factors involved in inflammation and fibrosis (Egr-1, POU1F1)
ClueGo Fig. 3B UT-encoded genes and up-regulated SGs in ESRD are shared in some pro-inflammatory pathways。
GEO2R Table 4a, Table 4bA and 4B Proinflammatory uremic cytokines IL1b and IL18 in UTs can amplify the upregulation of SGs in ESRD
IPA Table4C Cytokines can be modulated during CKD progression to induce imbalance of anti-inflammatory and proinflammatory function.