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Transforming Growth Factor-β and Long Non-coding RNA in Renal Inflammation and Fibrosis
Yue-Yu Gu1,2, Jing-Yun Dou1,3, Xiao-Ru Huang2,4
1Guangdong Provincial Key Laboratory of Clinical Research on Traditional Chinese Medicine Syndrome, Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Second Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, China.
Abstract:
Renal fibrosis is one of the most characterized pathological features in chronic kidney disease (CKD). Progressive fibrosis eventually leads to renal failure, leaving dialysis or allograft transplantation the only clinical option for CKD patients. Transforming growth factor-β (TGF-β) is the key mediator in renal fibrosis and is an essential regulator for renal inflammation. Therefore, the general blockade of the pro-fibrotic TGF-β may reduce fibrosis but may risk promoting renal inflammation and other side effects due to the diverse role of TGF-β in kidney diseases. Long non-coding RNAs (lncRNAs) are RNA transcripts with more than 200 nucleotides and have been regarded as promising therapeutic targets for many diseases. This review focuses on the importance of TGF-β and lncRNAs in renal inflammation, fibrogenesis, and the potential applications of TGF-β and lncRNAs as the therapeutic targets and biomarkers in renal fibrosis and CKD are highlighted.
Insights
Transforming growth factor-β (TGF-β) and long non-coding RNAs (lncRNAs) are key players in chronic kidney disease (CKD) fibrosis and inflammation. Targeting these molecules offers potential therapeutic strategies and biomarkers for kidney disease.
Area of Science:
- Nephrology
- Molecular Biology
- Genetics
Background:
- Renal fibrosis is a hallmark of chronic kidney disease (CKD), often leading to kidney failure.
- Transforming growth factor-β (TGF-β) is a critical mediator of renal fibrosis and inflammation.
- Broad TGF-β inhibition may cause adverse effects due to its diverse roles.
Purpose of the Study:
- To review the roles of TGF-β and long non-coding RNAs (lncRNAs) in renal fibrosis and inflammation.
- To highlight their potential as therapeutic targets and biomarkers for CKD.
Main Methods:
- Literature review focusing on TGF-β and lncRNAs in renal pathology.
- Analysis of the molecular mechanisms underlying renal fibrosis and inflammation.
- Evaluation of therapeutic and diagnostic potential.
Main Results:
- TGF-β is central to fibrogenesis and inflammation in the kidney.
- lncRNAs emerge as significant regulators in these processes.
- Both TGF-β and lncRNAs show promise as therapeutic targets and biomarkers.
Conclusions:
- Targeting TGF-β and lncRNAs presents a promising avenue for managing renal fibrosis in CKD.
- Further research into these molecules could lead to novel treatments and diagnostic tools for kidney diseases.
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