Evidence map›Paper›PMID 30943069›Full record

ReviewAmerican journal of physiology. Renal physiology2019

Targeting STAT3 signaling in kidney disease.

Jesse Pace, Praharshasai Paladugu, Bhaskar Das, John C He, Sandeep K Mallipattu

Open access · bronzeAbstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 4% 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

59 citing papers in PubMed, 2 syntheses or guidelines pooled it, 94 citations in OpenAlex.

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  10. International journal of molecular sciences · 2026
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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

5 authors at 3 institutions in 1 country.

Jesse PaceDivision of Nephrology, Department of Medicine, Stony Brook University , Stony Brook, New York.
Praharshasai PaladuguDivision of Nephrology, Department of Medicine, Stony Brook University , Stony Brook, New York.
Bhaskar DasDivision of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai , New York, New York.
John C HeDivision of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai , New York, New York.
Sandeep K MallipattuDivision of Nephrology, Department of Medicine, Stony Brook University , Stony Brook, New York.
Icahn School of Medicine at Mount Sinai · USStony Brook University · USNorthport VA Medical Center · US

Funding

Transcriptional control of mitochondrial function by KLF6 in diabetic kidney diseaseR01DK112984 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI Sandeep K Mallipattu · 2017 to 2026
$3.5M
Role of KLF15 in proximal tubule metabolismI01BX003698 · VA · NORTHPORT VA MEDICAL CENTER · PI Sandeep K Mallipattu · 2018 to 2026
–
BLRD VA I01 BX003698NIDDK NIH HHS R01 DK112984
6 · The paper itself

Abstract

The Janus kinase/signal transducer and activator of transcription (JAK/STAT) signaling pathway is a multifaceted transduction system that regulates cellular responses to incoming signaling ligands. STAT3 is a central member of the JAK/STAT signaling cascade and has long been recognized for its increased transcriptional activity in cancers and autoimmune disorders but has only recently been in the spotlight for its role in the progression of kidney disease. Although genetic knockout and manipulation studies have demonstrated the salutary benefits of inhibiting STAT3 activity in several kidney disease models, pharmacological inhibition has yet to make it to the clinical forefront. In recent years, significant effort has been aimed at suppressing STAT3 activation for treatment of cancers, which has led to the development of a wide variety of STAT3 inhibitors, but only a handful have been tested in kidney disease models. Here, we review the detrimental role of dysregulated STAT3 activation in a variety of kidney diseases and the current progress in the treatment of kidney diseases with pharmacological inhibition of STAT3 activity.

Indexed as

AnimalsHumansJanus KinasesKidneyKidney DiseasesMolecular Targeted TherapyRenal AgentsSignal TransductionSTAT3 Transcription FactorJanus KinasesRenal AgentsSTAT3 protein, humanSTAT3 Transcription Factorglomerulosclerosiskidney diseasepodocytesproteinuriasignal transducer and activator of transcription 3

Identifiers

PMID30943069
PMCPMC6620596
OpenAlexW2926512122

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.