Evidence map›Paper›PMID 12107109›Full record

ArticleThe American journal of pathology2002

Characterization of gene expression induced by RET with MEN2A or MEN2B mutation.

Tsuyoshi Watanabe, Masatoshi Ichihara, Mizuo Hashimoto, Keiko Shimono, Yoshie Shimoyama, Tetsuro Nagasaka, Yoshiki Murakumo, Hideki Murakami, Hideshi Sugiura, Hisashi Iwata and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 77 citations in OpenAlex.

  1. Fracture Risk in Pediatric Patients With MEN2B.The Journal of clinical endocrinology and metabolism · 2022
    Article
  2. Review
  3. Expression, function and clinical application of stanniocalcin-1 in cancer.Journal of cellular and molecular medicine · 2020
    Review
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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

12 authors at 2 institutions in 2 countries.

Tsuyoshi WatanabeDepartment of Pathology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masatoshi Ichihara
Mizuo Hashimoto
Keiko Shimono
Yoshie Shimoyama
Tetsuro Nagasaka
Yoshiki Murakumo
Hideki Murakami
Hideshi Sugiura
Hisashi Iwata
Naoki Ishiguro
Masahide Takahashi
Nagoya University · JPOrthopedic One · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germ-line point mutations of the RET gene are responsible for multiple endocrine neoplasia (MEN) type 2A and 2B that develop medullary thyroid carcinoma and pheochromocytoma. We performed a differential display analysis of gene expression using NIH 3T3 cells expressing the RET-MEN2A or RET-MEN2B mutant proteins. As a consequence, we identified 10 genes induced by both mutant proteins and eight genes repressed by them. The inducible genes include cyclin D1, cathepsins B and L, and cofilin genes that are known to be involved in cell growth, tumor progression, and invasion. In contrast, the repressed genes include type I collagen, lysyl oxidase, annexin I, and tissue inhibitor of matrix metalloproteinase 3 (TIMP3) genes that have been implicated in tumor suppression. In addition, six RET-MEN2A- and five RET-MEN2B-inducible genes were identified. Among 21 genes induced by RET-MEN2A and/or RET-MEN2B, six genes including cyclin D1, cathepsin B, cofilin, ring finger protein 11 (RNF11), integrin-alpha6, and stanniocalcin 1 (STC1) genes were also induced in TGW human neuroblastoma cells in response to glial cell line-derived neurotrophic factor stimulation. Because the STC1 gene was found to be highly induced by both RET-MEN2B and glial cell line-derived neurotrophic factor stimulation, and the expression of its product was detected in medullary thyroid carcinoma with the MEN2B mutation by immunohistochemistry, this may suggest a possible role for STC1 in the development of MEN 2B phenotype.

Indexed as

Drosophila ProteinsGene ExpressionNerve Growth Factors3T3 CellsAnimalsCarcinoma, MedullaryData DisplayGene Expression RegulationGlial Cell Line-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic Factor ReceptorsGlycoproteinsHormonesMiceMultiple Endocrine Neoplasia Type 2aMultiple Endocrine Neoplasia Type 2bMutationDrosophila ProteinsGdnf protein, mouseGlial Cell Line-Derived Neurotrophic FactorGlial Cell Line-Derived Neurotrophic Factor ReceptorsGlycoproteinsHormonesNerve Growth FactorsNerve Tissue ProteinsProto-Oncogene ProteinsProto-Oncogene Proteins c-retReceptor Protein-Tyrosine KinasesRet protein, DrosophilaRet protein, mouseteleocalcin

Identifiers

PMID12107109
PMCPMC1850689
OpenAlexW2077783195

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.