Evidence map›Paper›PMID 7559744›Full record

ArticleJournal of cancer research and clinical oncology1995

Renal carcinogenesis in the Eker rat.

O Hino, E Kobayashi, M Nishizawa, Y Kubo, T Kobayashi, Y Hirayama, S Takai, Y Kikuchi, H Tsuchiya, K Orimoto

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 57 citations in OpenAlex.

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  14. Diagnostic tumor marker of asbestos-related mesothelioma.Environmental health and preventive medicine · 2008
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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

10 authors at 1 institution in 1 country.

O HinoDepartment of Experimental Pathology, Cancer Institute, Tokyo, Japan.
E Kobayashi
M Nishizawa
Y Kubo
T Kobayashi
Y Hirayama
S Takai
Y Kikuchi
H Tsuchiya
K Orimoto
The Cancer Institute Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Eker rat hereditary renal carcinoma is an excellent example of a Mendelian dominant predisposition to a specific cancer in an experimental animal. We recently reported that a germline insertion in the rat homologue of the human tuberous sclerosis (TSC2) gene gives rise to the dominantly inherited cancer in the Eker rat model. The function of the TSC2/Tsc2 gene product (called "tuberine" in the human case) is not yet understood, although it contains a short amino acid sequence homologous to the ras family GTPase-activating proteins (GAP3). In the study, we isolated subtracted cDNA clones having increased expression in Eker renal carcinoma cells, using a modified representational difference analysis method to search for additional genes specifically involved in renal carcinogenesis. Here we identified four genes: the third component of the complement (C3) gene, the fos-related antigen I (fra-1) gene, an unknown gene (designated as being expressed in renal carcinoma: erc) and the calpactine I heavy-chain (Annexin II) gene.

Indexed as

AnimalsAnnexin A2Base SequenceChromosomes, Human, Pair 16DNA, ComplementaryDNA PrimersFos-Related Antigen 1Gene Expression Regulation, NeoplasticGenes, DominantHumansKidney NeoplasmsMaleMesothelinMolecular Sequence DataProto-Oncogene Proteins c-fosRatsAnnexin A2DNA, ComplementaryDNA PrimersFos-Related Antigen 1MesothelinMsln protein, ratProto-Oncogene Proteins c-fosRNA, MessengerRNA, Neoplasm

Identifiers

PMID7559744
PMCPMC12200376
OpenAlexW2005678942

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.