Evidence map›Paper›PMID 29449563›Full record

ArticleCell death & disease2018

Cinacalcet-mediated activation of the CaMKKβ-LKB1-AMPK pathway attenuates diabetic nephropathy in db/db mice by modulation of apoptosis and autophagy.

Ji Hee Lim, Hyung Wook Kim, Min Young Kim, Tae Woo Kim, Eun Nim Kim, Yaeni Kim, Sungjin Chung, Young Soo Kim, Bum Soon Choi, Yong-Soo Kim and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Guideline
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  9. Article
  10. Autophagy, Pyroptosis and Ferroptosis are Rising Stars in the Pathogenesis of Diabetic Nephropathy.Diabetes, metabolic syndrome and obesity : targets and therapy · 2024
    Review
  11. Article
  12. Article
  13. Redox regulation in diabetic kidney disease.American journal of physiology. Renal physiology · 2023
    Review
  14. Article
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  16. Review
  17. Article
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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

13 authors at 3 institutions in 1 country.

Ji Hee LimDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Hyung Wook KimDivision of Nephrology, Department of Internal Medicine, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Suwon, Korea.
Min Young KimDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Tae Woo KimDepartment of Hematology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Eun Nim KimDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Yaeni KimDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Sungjin ChungDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.ORCID 0000-0002-9886-8339
Young Soo KimDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Bum Soon ChoiDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Yong-Soo KimDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Yoon Sik ChangDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea.
Hye Won KimDepartment of Rehabilitation Medicine, College of Medicine, The Catholic University of Korea, Bucheon, Korea.
Cheol Whee ParkDivision of Nephrology, Department of Internal Medicine, The Catholic University of Korea, Seoul, Korea. cheolwhee@hanmail.net.
Catholic University of Korea · KRThe Catholic University of Korea St. Vincent's Hospital · KRThe Catholic University of Korea Seoul St. Mary's Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apoptosis and autophagy are harmoniously regulated biological processes for maintaining tissue homeostasis. AMP-activated protein kinase (AMPK) functions as a metabolic sensor to coordinate cellular survival and function in various organs, including the kidney. We investigated the renoprotective effects of cinacalcet in high-glucose treated human glomerular endothelial cells (HGECs), murine podocytes and C57BLKS/J-db/db mice. In cultured HGECs and podocytes, cinacalcet decreased oxidative stress and apoptosis and increased autophagy that were attributed to the increment of intracellular Ca

Indexed as

AlbuminuriaAMP-Activated Protein KinasesAnimalsApoptosisAutophagyCalcium-Calmodulin-Dependent Protein Kinase KinaseCells, CulturedCinacalcetDiabetic NephropathiesDisease Models, AnimalEndothelial CellsEnzyme ActivationHumansKidney GlomerulusMaleMice, Inbred C57BLAMP-Activated Protein KinasesCalcium-Calmodulin-Dependent Protein Kinase KinaseCinacalcetNitric Oxide Synthase Type IIINos3 protein, mouseProtein Serine-Threonine KinasesStk11 protein, mouse

Identifiers

PMID29449563
PMCPMC5833853
OpenAlexW2789348215

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.