Evidence map›Paper›PMID 25188299›Full record

ArticlePloS one2014

Analysis of gene expression profiles of soft tissue sarcoma using a combination of knowledge-based filtering with integration of multiple statistics.

Anna Takahashi, Robert Nakayama, Nanako Ishibashi, Ayano Doi, Risa Ichinohe, Yoriko Ikuyo, Teruyoshi Takahashi, Shigetaka Marui, Koji Yasuhara, Tetsuro Nakamura and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.9field-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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Cell journal · 2022
    Article
  4. Article
  5. Article
  6. Metabolic landscapes in sarcomas.Journal of hematology & oncology · 2021
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. BioMed research international · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Peroxiredoxin 1 - an antioxidant enzyme in cancer.Journal of cellular and molecular medicine · 2017
    Review
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 6 institutions in 2 countries.

Anna TakahashiPlant Biology Research Center, Chubu University, Kasugai, Aichi, Japan.
Robert NakayamaDivision of Genetics, National Cancer Center Research Institute, Tokyo, Japan; Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Nanako IshibashiDivision of Biological Science, Graduate School of Science, Nagoya University, Nagoya, Aichi, Japan.
Ayano DoiDivision of Genetics, National Cancer Center Research Institute, Tokyo, Japan; Faculty of Horticulture, Chiba University, Matsudo, Chiba, Japan.
Risa IchinoheDivision of Genetics, National Cancer Center Research Institute, Tokyo, Japan; Faculty of Horticulture, Chiba University, Matsudo, Chiba, Japan.
Yoriko IkuyoGraduate School of Bioscience and Biotechnology, Chubu University, Kasugai, Aichi, Japan.
Teruyoshi TakahashiGraduate School of Bioscience and Biotechnology, Chubu University, Kasugai, Aichi, Japan.
Shigetaka MaruiGraduate School of Bioscience and Biotechnology, Chubu University, Kasugai, Aichi, Japan.
Koji YasuharaGraduate School of Bioscience and Biotechnology, Chubu University, Kasugai, Aichi, Japan.
Tetsuro NakamuraGraduate School of Bioscience and Biotechnology, Chubu University, Kasugai, Aichi, Japan.
Shintaro SugitaDepartment of Surgical Pathology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan.
Hiromi SakamotoDivision of Genetics, National Cancer Center Research Institute, Tokyo, Japan.
Teruhiko YoshidaDivision of Genetics, National Cancer Center Research Institute, Tokyo, Japan.
Tadashi HasegawaDepartment of Surgical Pathology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan; Pathology Division, National Cancer Center Hospital, Tokyo, Japan.
Hiro TakahashiPlant Biology Research Center, Chubu University, Kasugai, Aichi, Japan; Division of Genetics, National Cancer Center Research Institute, Tokyo, Japan; Graduate School of Horticulture, Chiba University, Matsudo, Chiba, Japan.
Chubu University · JPChiba Cancer Center · JPNational Cancer Centre Japan · JPSapporo Medical University · JPNagoya University · JPNational Cancer Research Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The diagnosis and treatment of soft tissue sarcomas (STS) have been difficult. Of the diverse histological subtypes, undifferentiated pleomorphic sarcoma (UPS) is particularly difficult to diagnose accurately, and its classification per se is still controversial. Recent advances in genomic technologies provide an excellent way to address such problems. However, it is often difficult, if not impossible, to identify definitive disease-associated genes using genome-wide analysis alone, primarily because of multiple testing problems. In the present study, we analyzed microarray data from 88 STS patients using a combination method that used knowledge-based filtering and a simulation based on the integration of multiple statistics to reduce multiple testing problems. We identified 25 genes, including hypoxia-related genes (e.g., MIF, SCD1, P4HA1, ENO1, and STAT1) and cell cycle- and DNA repair-related genes (e.g., TACC3, PRDX1, PRKDC, and H2AFY). These genes showed significant differential expression among histological subtypes, including UPS, and showed associations with overall survival. STAT1 showed a strong association with overall survival in UPS patients (logrank p = 1.84 × 10(-6) and adjusted p value 2.99 × 10(-3) after the permutation test). According to the literature, the 25 genes selected are useful not only as markers of differential diagnosis but also as prognostic/predictive markers and/or therapeutic targets for STS. Our combination method can identify genes that are potential prognostic/predictive factors and/or therapeutic targets in STS and possibly in other cancers. These disease-associated genes deserve further preclinical and clinical validation.

Indexed as

Gene Expression Regulation, NeoplasticSoftwareAlgorithmsBiomarkers, TumorFemaleGene Expression ProfilingHumansKnowledge BasesMaleMiddle AgedNeoplasm ProteinsOligonucleotide Array Sequence AnalysisPrognosisSarcomaSoft Tissue NeoplasmsSTAT1 Transcription FactorBiomarkers, TumorNeoplasm ProteinsSTAT1 protein, humanSTAT1 Transcription Factor

Identifiers

PMID25188299
PMCPMC4154757
OpenAlexW1967297034

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.