Evidence map›Paper›PMID 29113136›Full record

SynthesisInternational journal of molecular sciences2017

Discovering the Deregulated Molecular Functions Involved in Malignant Transformation of Endometriosis to Endometriosis-Associated Ovarian Carcinoma Using a Data-Driven, Function-Based Analysis.

Chia-Ming Chang, Yi-Ping Yang, Jen-Hua Chuang, Chi-Mu Chuang, Tzu-Wei Lin, Peng-Hui Wang, Mu-Hsien Yu, Cheng-Chang Chang

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Immunology and ovarian cancers.Journal of the Chinese Medical Association : JCMA · 2020
    Review
  11. Article
  12. Aberrant sialylation in ovarian cancers.Journal of the Chinese Medical Association : JCMA · 2020
    Review
  13. The recent progress and therapy in endometriosis-associated ovarian cancer.Journal of the Chinese Medical Association : JCMA · 2020
    Review
  14. Article
  15. Article
  16. 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

8 authors at 2 institutions in 1 country.

Chia-Ming ChangSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. cm_chang@vghtpe.gov.tw.
Yi-Ping YangSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. molly0103@gmail.com.
Jen-Hua ChuangSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. chuangjenhua5@gmail.com.
Chi-Mu ChuangSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. cmjuang@gmail.com.
Tzu-Wei LinSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. backyard0826@gmail.com.
Peng-Hui WangSchool of Medicine, National Yang-Ming University, Taipei 112, Taiwan. phwang@vghtpe.gov.tw.
Mu-Hsien YuDepartment of Obstetrics and Gynecology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan. hsienhui@ms15.hinet.net.
Cheng-Chang ChangDepartment of Obstetrics and Gynecology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan. obsgynchang@gmail.com.
Tri-Service General Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical characteristics of clear cell carcinoma (CCC) and endometrioid carcinoma EC) are concomitant with endometriosis (ES), which leads to the postulation of malignant transformation of ES to endometriosis-associated ovarian carcinoma (EAOC). Different deregulated functional areas were proposed accounting for the pathogenesis of EAOC transformation, and there is still a lack of a data-driven analysis with the accumulated experimental data in publicly-available databases to incorporate the deregulated functions involved in the malignant transformation of EOAC. We used the microarray gene expression datasets of ES, CCC and EC downloaded from the National Center for Biotechnology Information Gene Expression Omnibus (NCBI GEO) database. Then, we investigated the pathogenesis of EAOC by a data-driven, function-based analytic model with the quantified molecular functions defined by 1454 Gene Ontology (GO) term gene sets. This model converts the gene expression profiles to the functionome consisting of 1454 quantified GO functions, and then, the key functions involving the malignant transformation of EOAC can be extracted by a series of filters. Our results demonstrate that the deregulated oxidoreductase activity, metabolism, hormone activity, inflammatory response, innate immune response and cell-cell signaling play the key roles in the malignant transformation of EAOC. These results provide the evidence supporting the specific molecular pathways involved in the malignant transformation of EAOC.

Indexed as

CarcinomaCell Transformation, NeoplasticEndometriosisFemaleGene Expression Regulation, NeoplasticHumansMicroarray AnalysisNeoplasm ProteinsOvarian NeoplasmsTranscriptomeNeoplasm Proteinsdata-driven analysisendometriosisfunction-basedGene Ontologymicroarray gene expression datasetsovarian carcinoma

Identifiers

PMID29113136
PMCPMC5713314
OpenAlexW2767684642

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.