Evidence map›Paper›PMID 22355695›Full record

ArticleScientific reports2011

Potential role of LMP2 as tumor-suppressor defines new targets for uterine leiomyosarcoma therapy.

Takuma Hayashi, Akiko Horiuchi, Kenji Sano, Nobuyoshi Hiraoka, Mari Kasai, Tomoyuki Ichimura, Tamotsu Sudo, Yoh-Ichi Tagawa, Ryuichiro Nishimura, Osamu Ishiko and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 59 citations in OpenAlex.

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  18. Biological characterization of soft tissue sarcomas.Annals of translational medicine · 2015
    Article
  19. Article
  20. Potential biomarker for human uterine leiomyosarcoma.Journal of clinical medicine research · 2014
    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

15 authors at 10 institutions in 2 countries.

Takuma HayashiDept. of Immunology and Infectious Disease, Shinshu University Graduate School of Medicine. takumah@shinshu-u.ac.jp
Akiko Horiuchi
Kenji Sano
Nobuyoshi Hiraoka
Mari Kasai
Tomoyuki Ichimura
Tamotsu Sudo
Yoh-Ichi Tagawa
Ryuichiro Nishimura
Osamu Ishiko
Yae Kanai
Nobuo Yaegashi
Hiroyuki Aburatani
Tanri Shiozawa
Ikuo Konishi
Osaka City University · JPHyogo Prefectural Cancer Center · JPNational Cancer Research Institute · GBShinshu University · JPKyoto University · JPŌtani University · JPShinshu University Hospital · JPThe University of Tokyo · JPTohoku University · JPTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the majority of smooth muscle neoplasms found in the uterus are benign, uterine leiomyosarcoma (LMS) is extremely malignant, with high rates of recurrence and metastasis. We earlier reported that mice with a homozygous deficiency for LMP2, an interferon (IFN)-γ-inducible factor, spontaneously develop uterine LMS. The IFN-γ pathway is important for control of tumor growth and invasion and has been implicated in several cancers. In this study, experiments with human and mouse uterine tissues revealed a defective LMP2 expression in human uterine LMS that was traced to the IFN-γ pathway and the specific effect of JAK-1 somatic mutations on the LMP2 transcriptional activation. Furthermore, analysis of a human uterine LMS cell line clarified the biological significance of LMP2 in malignant myometrium transformation and cell cycle, thus implicating LMP2 as an anti-tumorigenic candidate. This role of LMP2 as a tumor suppressor may lead to new therapeutic targets in human uterine LMS.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCysteine EndopeptidasesFemaleGenes, Tumor SuppressorHumansInterferon-gammaLeiomyosarcomaMiceMutationMyometriumTranscriptional ActivationTransfectionUterine NeoplasmsUterusCysteine EndopeptidasesInterferon-gammaLMP-2 protein

Identifiers

PMID22355695
PMCPMC3240965
OpenAlexW2006260156

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.