Evidence map›Paper›PMID 23922129›Full record

ArticlePhysiological genomics2013

Cell cycle arrest in a model of colistin nephrotoxicity.

Michael T Eadon, Bradley K Hack, Jessy J Alexander, Chang Xu, M Eileen Dolan, Patrick N Cunningham

Open access · greenAbstract read
In one paragraph

Article in Physiological genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

  1. Molecular mechanisms attributed to colistin renal proximal tubular epithelial cytotoxicity.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2025
    Review
  2. Preclinical evaluation of tridecaptin M:Antimicrobial agents and chemotherapy · 2025
    Article
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  10. Adverse effects of polymyxin B administration to healthy horses.Journal of veterinary internal medicine · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Review
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  16. Review
  17. Rat models of colistin nephrotoxicity: previous experimental researches and future perspectives.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2019
    Review
  18. Article
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  20. 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

6 authors at 3 institutions in 1 country.

Michael T EadonDivisions of Nephrology and Clinical Pharmacology, Indiana University, Indianapolis, Indiana;
Bradley K Hack
Jessy J Alexander
Chang Xu
M Eileen Dolan
Patrick N Cunningham
Indiana University – Purdue University Indianapolis · USUniversity at Buffalo, State University of New York · USUniversity of Chicago · US

Funding

CLINICAL THERAPEUTICST32GM007019 · NIGMS · UNIVERSITY OF CHICAGO · PI Peter Hugh O'Donnell, MARK J RATAIN · 1985 to 2026
$8.7M
Endothelial Injury in Endotoxin-Induced Acute Renal FailureR01DK080863 · NIDDK · UNIVERSITY OF CHICAGO · PI CUNNINGHAM, PATRICK N · 2010 to 2014
$1.7M
NIDDK NIH HHS R01 DK080863NIDDK NIH HHS R01DK-080863NIGMS NIH HHS T32GM-007019
6 · The paper itself

Abstract

Colistin (polymixin E) is an antibiotic prescribed with resurging frequency for multidrug resistant gram negative bacterial infections. It is associated with nephrotoxicity in humans in up to 55% of cases. Little is known regarding genes involved in colistin nephrotoxicity. A murine model of colistin-mediated kidney injury was developed. C57/BL6 mice were administered saline or colistin at a dose of 16 mg/kg/day in 2 divided intraperitoneal doses and killed after either 3 or 15 days of colistin. After 15 days, mice exposed to colistin had elevated blood urea nitrogen (BUN), creatinine, and pathologic evidence of acute tubular necrosis and apoptosis. After 3 days, mice had neither BUN elevation nor substantial pathologic injury; however, urinary neutrophil gelatinase-associated lipocalin was elevated (P = 0.017). An Illumina gene expression array was performed on kidney RNA harvested 72 h after first colistin dose to identify differentially expressed genes early in drug treatment. Array data revealed 21 differentially expressed genes (false discovery rate < 0.1) between control and colistin-exposed mice, including LGALS3 and CCNB1. The gene signature was significantly enriched for genes involved in cell cycle proliferation. RT-PCR, immunoblot, and immunostaining validated the relevance of key genes and proteins. This murine model offers insights into the potential mechanism of colistin-mediated nephrotoxicity. Further studies will determine whether the identified genes play a causative or protective role in colistin-induced nephrotoxicity.

Indexed as

AnimalsBody WeightCell Cycle CheckpointsCluster AnalysisColistinDisease Models, AnimalGalectin 3Gene Expression ProfilingIn Situ Nick-End LabelingKidneyKidney TubulesMaleMiceMice, Inbred C57BLNecrosisProliferating Cell Nuclear AntigenColistinGalectin 3Proliferating Cell Nuclear Antigencell cyclecolistingalectin-3nephrotoxicitypolymyxin Erenal failure

Identifiers

PMID23922129
PMCPMC3798781
OpenAlexW2108969659

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.