Evidence map›Paper›PMID 35096927›Full record

ArticleFrontiers in nutrition2021

Excessive Inorganic Phosphate Burden Perturbed Intracellular Signaling: Quantitative Proteomics and Phosphoproteomics Analyses.

Rebecca Hetz, Erik Beeler, Alexis Janoczkin, Spencer Kiers, Ling Li, Belinda B Willard, Mohammed S Razzaque, Ping He

Abstract read
In one paragraph

Article in Frontiers in nutrition, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Vitamin D and Mineral Ion Regulation.Advances in experimental medicine and biology · 2026
    Review
  4. Article
  5. Article
  6. Phosphate Burden and Organ Dysfunction.Frontiers in aging · 2022
    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

8 authors.

Rebecca HetzDepartment of Biochemistry, Lake Erie College of Osteopathic Medicine, Erie, PA, United States.
Erik BeelerDepartment of Biochemistry, Lake Erie College of Osteopathic Medicine, Erie, PA, United States.
Alexis JanoczkinDepartment of Biochemistry, Lake Erie College of Osteopathic Medicine, Erie, PA, United States.
Spencer KiersDepartment of Biochemistry, Lake Erie College of Osteopathic Medicine, Erie, PA, United States.
Ling LiProteomics and Metabolomics Core, Cleveland Clinic Lerner Research Institute, Cleveland, OH, United States.
Belinda B WillardProteomics and Metabolomics Core, Cleveland Clinic Lerner Research Institute, Cleveland, OH, United States.
Mohammed S RazzaqueDepartment of Pathology, Lake Erie College of Osteopathic Medicine, Erie, PA, United States.
Ping HeDepartment of Biochemistry, Lake Erie College of Osteopathic Medicine, Erie, PA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inorganic phosphate (Pi) is an essential nutrient for the human body which exerts adverse health effects in excess and deficit. High Pi-mediated cytotoxicity has been shown to induce systemic organ damage, though the underlying molecular mechanisms are poorly understood. In this study, we employed proteomics and phosphoproteomics to analyze Pi-mediated changes in protein abundance and phosphorylation. Bioinformatic analyses and literature review revealed that the altered proteins and phosphorylation were enriched in signaling pathways and diverse biological processes. Western blot analysis confirms the extensive change in protein level and phosphorylation in key effectors that modulate pre-mRNA alternative splicing. Global proteome and phospho-profiling provide a bird-eye view of excessive Pi-rewired cell signaling networks, which deepens our understanding of the molecular mechanisms of phosphate toxicity.

Indexed as

alternative splicecell signalingcytotoxicityinorganic phosphatephosphoproteomicsproteomics

Identifiers

PMID35096927
PMCPMC8795896

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Registered trials

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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.