Evidence map›Paper›PMID 34360646›Full record

ReviewInternational journal of molecular sciences2021

TGF-Beta as a Master Regulator of Diabetic Nephropathy.

Li Wang, Hong-Lian Wang, Tong-Tong Liu, Hui-Yao Lan

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 3 pooled it
8.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

114 citing papers in PubMed, 3 syntheses or guidelines pooled it, 171 citations in OpenAlex.

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54 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Li WangResearch Center for Integrative Medicine, Affiliated Traditional Medicine Hospital of Southwest Medical University, Luzhou 646000, China.ORCID 0000-0003-3881-3149
Hong-Lian WangResearch Center for Integrative Medicine, Affiliated Traditional Medicine Hospital of Southwest Medical University, Luzhou 646000, China.ORCID 0000-0003-1169-176X
Tong-Tong LiuResearch Center for Integrative Medicine, Affiliated Traditional Medicine Hospital of Southwest Medical University, Luzhou 646000, China.
Hui-Yao LanDepartment of Medicine and Therapeutics and Li Ka Shing Institute of Health Sciences, Chinese University of Hong Kong, Hong Kong 999077, China.ORCID 0000-0003-4283-9755
Southwest Medical University · CNChinese University of Hong Kong · HK

Funding

Research Grants Council, University Grants Committee 14163317, 14117418, 14104019, R4012-18, C7018-16Gthe Department of Science and Technology of Luzhou City 2018LZXNYD-PT03, 2020LZXNYDJ15the Guangdong-Hong Kong-Macao-Joint Labs Program from Guangdong Science and Technology 2019B121205005the Health and Medical Research Fund of Hong Kong 05161326, 14152321, 07180516the Lui Che Woo Institute of Innovative Medicine (CARE program) of the Chinese University of Hong Kong NAthe Luzhou Municipal-Southwest Medical University Joint Special Grant for the High-level Talents HYL Teamthe research grant of Southwest Medical University 2019ZZD010
6 · The paper itself

Abstract

Diabetic nephropathy (DN) is one of the most common complications in diabetes mellitus and the leading cause of end-stage renal disease. TGF-β is a pleiotropic cytokine and has been recognized as a key mediator of DN. However, anti-TGF-β treatment for DN remains controversial due to the diverse role of TGF-β1 in DN. Thus, understanding the regulatory role and mechanisms of TGF-β in the pathogenesis of DN is the initial step towards the development of anti-TGF-β treatment for DN. In this review, we first discuss the diverse roles and signaling mechanisms of TGF-β in DN by focusing on the latent versus active TGF-β1, the TGF-β receptors, and the downstream individual Smad signaling molecules including Smad2, Smad3, Smad4, and Smad7. Then, we dissect the regulatory mechanisms of TGF-β/Smad signaling in the development of DN by emphasizing Smad-dependent non-coding RNAs including microRNAs and long-non-coding RNAs. Finally, the potential therapeutic strategies for DN by targeting TGF-β signaling with various therapeutic approaches are discussed.

Indexed as

AnimalsDiabetic NephropathiesHumansSignal TransductionTransforming Growth Factor betaTransforming Growth Factor betadiabetic nephropathyfibrosisinflammationSmadTGF-β signaling

Identifiers

PMID34360646
PMCPMC8345981
OpenAlexW3185611478

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.