Evidence map›Paper›PMID 11092979›Full record

ArticleJapanese journal of cancer research : Gann2000

Mapping of melanoma modifier loci in RET transgenic mice.

T A Dragani, B Peissel, N Zanesi, A Aloisi, Y Dai, M Kato, H Suzuki, I Nakashima

Open access · greenAbstract read
In one paragraph

Article in Japanese journal of cancer research : Gann, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. How much do we know about the metastatic process?Clinical & experimental metastasis · 2024
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  4. Immune predictors of cancer progression.Immunologic research · 2012
    Review
  5. Article
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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

8 authors at 3 institutions in 3 countries.

T A DraganiDepartment of Experimental Oncology, Istituto Nazionale Tumori, Via G. Venezian Milan, Italy. dragani@istitutotumori.mi.it
B Peissel
N Zanesi
A Aloisi
Y Dai
M Kato
H Suzuki
I Nakashima
Nagoya University · JPFondazione IRCCS Istituto Nazionale dei Tumori · ITTumori Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transgenic mice carrying the RET oncogene under the control of the metallothionein promoter exhibit severe pigmentation of the whole skin and melanocytic tumors. The genetic background influences melanoma development in RET mice; founder mice crossed with BALB/c mice show decreased incidence and increased latency of melanocytic tumors, whereas progeny of C57BL/6 mice show the opposite effect. Using partially congenic RET mice on a C57BL/6 genetic background (N3/RET mice), we studied genetic linkage in (N3/RETxBALB/c)xN3/RET backcross mice. We mapped three melanoma modifier loci, on chromosome 1 (Melm1 and Melm2) and chromosome 11 (Melm3), that are linked with early melanoma incidence and latency. Mapping of Melm loci and of five additional regions on chromosomes 6, 8, 9, 12, and 13 indicated allelic imbalance in N3/RET mice, with a significant excess of BALB/c alleles, suggesting the presence of additional putative melanoma modifier loci on these chromosomes.

Indexed as

Drosophila ProteinsGenetic LinkageAllelic ImbalanceAnimalsChromosome MappingCrosses, GeneticFemaleInbreedingMaleMelanoma, ExperimentalMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicPhenotypeProto-Oncogene ProteinsDrosophila ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-retReceptor Protein-Tyrosine KinasesRet protein, DrosophilaRet protein, mouse

Identifiers

PMID11092979
PMCPMC5926280
OpenAlexW2020523519

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.