Evidence map›Paper›PMID 33853949›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

Orphan nuclear receptor ERR-γ regulates hepatic FGF23 production in acute kidney injury.

Kamalakannan Radhakrishnan, Yong-Hoon Kim, Yoon Seok Jung, Don-Kyu Kim, Soon-Young Na, Daejin Lim, Dong Hun Kim, Jina Kim, Hyung-Seok Kim, Hyon E Choy and 10 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  12. Regulation of FGF23: Beyond Bone.Current osteoporosis reports · 2021
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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

20 authors at 6 institutions in 2 countries.

Kamalakannan RadhakrishnanSchool of Biological Sciences and Technology, Chonnam National University, 61186 Gwangju, Republic of Korea.ORCID 0000-0002-0890-8692
Yong-Hoon KimLaboratory Animal Resource Center, Korea Research Institute of Bioscience and Biotechnology, 34141 Daejeon, Republic of Korea.
Yoon Seok JungSchool of Biological Sciences and Technology, Chonnam National University, 61186 Gwangju, Republic of Korea.
Don-Kyu KimDepartment of Molecular Biotechnology, Chonnam National University, 61186 Gwangju, Republic of Korea.ORCID 0000-0002-6251-6438
Soon-Young NaSchool of Biological Sciences and Technology, Chonnam National University, 61186 Gwangju, Republic of Korea.
Daejin LimDepartment of Microbiology, Chonnam National University Medical School, 61468 Gwangju, Republic of Korea.
Dong Hun KimDepartment of Biomedical Science, Graduate School, Kyungpook National University, 41404 Daegu, Republic of Korea.ORCID 0000-0003-0618-021X
Jina KimNew Drug Development Center, Daegu Gyeongbuk Medical Innovation Foundation, 41061 Daegu, Republic of Korea.
Hyung-Seok KimDepartment of Forensic Medicine, Chonnam National University Medical School, 61468 Gwangju, Republic of Korea.
Hyon E ChoyDepartment of Microbiology, Chonnam National University Medical School, 61468 Gwangju, Republic of Korea.
Sung Jin ChoNew Drug Development Center, Daegu Gyeongbuk Medical Innovation Foundation, 41061 Daegu, Republic of Korea.
In-Kyu LeeLeading-edge Research Center for Drug Discovery and Development for Diabetes and Metabolic Disease, Kyungpook National University Hospital, 41404 Daegu, Republic of Korea.ORCID 0000-0002-2261-7269
Şamil AyvazDepartment of Medicine II, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.
Stefanie NittkaInstitute for Clinical Chemistry, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany.
Danilo FliserDepartment of Internal Medicine IV, Nephrology and Hypertension, Saarland University, D-66421 Homburg/Saar, Germany.
Stefan J SchunkDepartment of Internal Medicine IV, Nephrology and Hypertension, Saarland University, D-66421 Homburg/Saar, Germany.
Thimoteus SpeerDepartment of Internal Medicine IV, Nephrology and Hypertension, Saarland University, D-66421 Homburg/Saar, Germany.
Steven DooleyDepartment of Medicine II, Medical Faculty Mannheim, Heidelberg University, 68167 Mannheim, Germany; steven.dooley@medma.uni-heidelberg.de chullee@kribb.re.kr hsc@chonnam.ac.kr.ORCID 0000-0002-4840-6240
Chul-Ho LeeLaboratory Animal Resource Center, Korea Research Institute of Bioscience and Biotechnology, 34141 Daejeon, Republic of Korea; steven.dooley@medma.uni-heidelberg.de chullee@kribb.re.kr hsc@chonnam.ac.kr.ORCID 0000-0002-6996-5746
Hueng-Sik ChoiSchool of Biological Sciences and Technology, Chonnam National University, 61186 Gwangju, Republic of Korea; steven.dooley@medma.uni-heidelberg.de chullee@kribb.re.kr hsc@chonnam.ac.kr.ORCID 0000-0002-3163-1572
Chonnam National University · KRHeidelberg University · DESaarland University · DEKorea Research Institute of Bioscience and Biotechnology · KRKyungpook National University Hospital · KRDaegu-Gyeongbuk Medical Innovation Foundation · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblast growth factor 23 (FGF23), a hormone generally derived from bone, is important in phosphate and vitamin D homeostasis. In acute kidney injury (AKI) patients, high-circulating FGF23 levels are associated with disease progression and mortality. However, the organ and cell type of FGF23 production in AKI and the molecular mechanism of its excessive production are still unidentified. For insight, we investigated folic acid (FA)-induced AKI in mice. Interestingly, simultaneous with FGF23, orphan nuclear receptor ERR-γ expression is increased in the liver of FA-treated mice, and ectopic overexpression of ERR-γ was sufficient to induce hepatic FGF23 production. In patients and in mice, AKI is accompanied by up-regulated systemic IL-6, which was previously identified as an upstream regulator of ERR-γ expression in the liver. Administration of IL-6 neutralizing antibody to FA-treated mice or of recombinant IL-6 to healthy mice confirms IL-6 as an upstream regulator of hepatic ERR-γ-mediated FGF23 production. A significant (

Indexed as

Acute Kidney InjuryAnimalsDisease Models, AnimalFibroblast Growth Factor-23Folic AcidInterleukin-6KidneyLiverMaleMiceMice, Inbred C57BLOrphan Nuclear ReceptorsReceptors, EstrogenTranscriptional ActivationEsrrg protein, mouseFgf23 protein, mouseFibroblast Growth Factor-23Folic AcidInterleukin-6Orphan Nuclear ReceptorsReceptors, Estrogenacute kidney injuryERR-γFGF23interleukin 6orphan nuclear receptor

Identifiers

PMID33853949
PMCPMC8072258
OpenAlexW3155069852

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.