Evidence map›Paper›PMID 18441261›Full record

ArticleToxicologic pathology2008

Spontaneous occurrence of a distinctive renal tubule tumor phenotype in rat carcinogenicity studies conducted by the national toxicology program.

Gordon C Hard, John Curtis Seely, Grace E Kissling, Laura J Betz

Open access · greenAbstract read
In one paragraph

Article in Toxicologic pathology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. 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

4 authors at 3 institutions in 2 countries.

Gordon C HardPrivate Consultant, Tairua, New Zealand. gordonhard@msn.com
John Curtis Seely
Grace E Kissling
Laura J Betz
Building Research Association of New Zealand · NZExperimental Pathology Laboratories · USNational Institute of Environmental Health Sciences · US

Funding

NIEHS ARCHIVES &SPECIMEN REPOSITORYN01ES095435 · NIEHS · EXPERIMENTAL PATHOLOGY LABORATORIES · PI HAMLIN, MELVIN · 1999 to 2000
$1.9M
Identifying And Evaluating Sources Of Variability In Rodent StudiesZIAES045003 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI KISSLING, GRACE E · 2009 to 2017
$712k
SOURCES OF VARIABILITY IN TUMOR INCIDENCE IN LONG TERM RODENT STUDIESZ01ES045003 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI KISSLING, GRACE E · 1997 to 2008
$127k
Intramural NIH HHS ZIA ES045003NIEHS NIH HHS N01 ES095435NIEHS NIH HHS N01-ES-95435
6 · The paper itself

Abstract

The Toxicology Data Management System (TDMS) of the National Toxicology Program, National Institutes of Environmental Health Sciences, National Institutes of Health, was surveyed for occurrence and distribution of a distinctive renal tubule tumor type in rats. The hallmark features of this tumor included eosinophilic/amphophilic staining, large finely granular cells, and numerous vacuoles and/or minilumens. It is referred to here as the amphophilic-vacuolar (AV) variant of renal tubule tumor. Of 154 studies in which renal tubule tumors had been recorded in the standard single sections of kidney in the TDMS, there were collectively 1012 rats with renal adenomas, carcinomas, or adenocarcinomas, and of these, 100 displayed the distinctive AV morphology, representing 74 studies involving mostly the F344 rat, but also the Sprague-Dawley and Wistar strains. The AV tumors (mainly adenomas but also some carcinomas) occurred usually as solitary lesions in the affected animals. However, they were multiple and bilateral in a few cases. They were equally distributed between the sexes, did not metastasize (at least to the lung), and were not associated with chronic progressive nephropathy. The distribution of this renal tumor type was random across studies and dose groups, underscoring the likelihood that it was of spontaneous origin and not chemically induced. Accordingly, it is suggested that this distinctive renal tumor phenotype be recorded as a separate category from conventional RTT when assessing the carcinogenic potential of a test compound.

Indexed as

AdenomaAnimalsCarcinogenicity TestsCarcinoma, Renal CellCytoplasmic GranulesFemaleKidney Failure, ChronicKidney NeoplasmsKidney TubulesMaleNational Institute of Environmental Health Sciences (U.S.)Neoplasms, Multiple PrimaryRatsRats, Inbred StrainsUnited StatesVacuoles

Identifiers

PMID18441261
PMCPMC2905801
OpenAlexW2154753141

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.