Evidence map›Paper›PMID 32686524›Full record

ReviewAmerican journal of physiology. Renal physiology2020

Phosphorylation of key podocyte proteins and the association with proteinuric kidney disease.

Di Feng

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Renal physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Protein lactylation in kidney diseases.Frontiers in cell and developmental biology · 2025
    Review
  8. Podocyte cell-specificPhysiological genomics · 2024
    Article
  9. Aging · 2023
    Article
  10. Review
  11. Review
  12. Investigations on the Changes of Serum Proteins in Rabbits afterEvidence-based complementary and alternative medicine : eCAM · 2022
    Article
  13. Review
  14. Cytoskeleton Rearrangements Modulate TRPC6 Channel Activity in Podocytes.International journal of molecular sciences · 2021
    Article
  15. Review
  16. Article
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

1 author at 1 institution in 1 country.

Di FengDivision of Nephrology, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts.ORCID 0000-0001-5652-176X
Beth Israel Deaconess Medical Center · US

Funding

RESEARCH TRAINING IN NEPHROLOGYT32DK007199 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI POLLAK, MARTIN R. · 1986 to 2022
$6.0M
Biological Mechanism of FSGS-1R37DK059588 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI POLLAK, MARTIN R. · 2011 to 2020
$4.0M
Biological mechanism of familial focal segmental glomerulosclerosis-1R01DK059588 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI POLLAK, MARTIN R. · 2001 to 2010
$3.5M
The interaction between mechanical forces and cytoskeletal impairments in podocyte mediated kidney diseaseK01DK114329 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI FENG, DI · 2018 to 2022
$744k
NIDDK NIH HHS K01 DK114329NIDDK NIH HHS R01 DK059588NIDDK NIH HHS R37 DK059588NIDDK NIH HHS T32 DK007199
6 · The paper itself

Abstract

Podocyte dysfunction contributes to proteinuric chronic kidney disease. A number of key proteins are essential for podocyte function, including nephrin, podocin, CD2-associated protein (CD2AP), synaptopodin, and α-actinin-4 (ACTN4). Although most of these proteins were first identified through genetic studies associated with human kidney disease, subsequent studies have identified phosphorylation of these proteins as an important posttranslational event that regulates their function. In this review, a brief overview of the function of these key podocyte proteins is provided. Second, the role of phosphorylation in regulating the function of these proteins is described. Third, the association between these phosphorylation pathways and kidney disease is reviewed. Finally, challenges and future directions in studying phosphorylation are discussed. Better characterization of these phosphorylation pathways and others yet to be discovered holds promise for translating this knowledge into new therapies for patients with proteinuric chronic kidney disease.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCytoskeletal ProteinsHumansKidney DiseasesKidney GlomerulusMembrane ProteinsPhosphorylationPodocytesAdaptor Proteins, Signal TransducingCD2-associated proteinCytoskeletal ProteinsMembrane Proteinsnephrinphosphorylationpodocyteproteinuric kidney diseaseslit diaphragmα-actinin-4

Identifiers

PMID32686524
PMCPMC7528399
OpenAlexW3044649216

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.