Evidence map›Paper›PMID 28811384›Full record

ArticleScience signaling2017

Loss of SPDEF and gain of TGFBI activity after androgen deprivation therapy promote EMT and bone metastasis of prostate cancer.

Wei-Yu Chen, Yuan-Chin Tsai, Hsiu-Lien Yeh, Florent Suau, Kuo-Ching Jiang, Ai-Ning Shao, Jiaoti Huang, Yen-Nien Liu

Abstract read
PubMed Publisher
In one paragraph

Article in Science signaling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
  6. Article
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  8. Article
  9. Article
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  11. Review
  12. Article
  13. Downregulation ofGenes & diseases · 2022
    Article
  14. Article
  15. Review
  16. Review
  17. Long noncoding RNAs in cancer metastasis.Nature reviews. Cancer · 2021
    Review
  18. Epigenetics in prostate cancer: clinical implications.Translational andrology and urology · 2021
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 3 countries.

Wei-Yu ChenDepartment of Pathology, Wan Fang Hospital, Taipei Medical University, Taipei 11031, Taiwan.ORCID http://orcid.org/0000-0003-3660-8045
Yuan-Chin TsaiGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan.
Hsiu-Lien YehInstitute of Information System and Applications, National Tsing Hua University, Hsinchu 30013, Taiwan.
Florent SuauDepartment of Microbiology, Faculty of Pharmacy, Dicle University, Diyarbakir 21280, Turkey.ORCID http://orcid.org/0000-0003-3870-2449
Kuo-Ching JiangGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan.
Ai-Ning ShaoGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan.
Jiaoti HuangDepartment of Pathology, Duke University Medical Center, Durham, NC 27710, USA.
Yen-Nien LiuGraduate Institute of Cancer Biology and Drug Discovery, College of Medical Science and Technology, Taipei Medical University, Taipei 11031, Taiwan. liuy@tmu.edu.tw.ORCID http://orcid.org/0000-0002-3102-8482
Taipei Medical University · TWDicle University · TRDuke Medical Center · USNational Tsing Hua University · TWWan Fang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Androgen deprivation therapy (ADT) targeting the androgen receptor (AR) is a standard therapeutic regimen for treating prostate cancer. However, most tumors progress to metastatic castration-resistant prostate cancer after ADT. We identified the type 1, 2, and 4 collagen-binding protein transforming growth factor-β (TGFβ)-induced protein (TGFBI) as an important factor in the epithelial-to-mesenchymal transition (EMT) and malignant progression of prostate cancer. In prostate cancer cell lines, AR signaling stimulated the activity of the transcription factor SPDEF, which repressed the expression of

Indexed as

Epithelial-Mesenchymal TransitionAndrogen AntagonistsAnimalsbetaIG-H3 ProteinBone NeoplasmsExtracellular Matrix ProteinsGene Expression Regulation, NeoplasticHumansMaleMiceMice, NudeProstatic NeoplasmsProto-Oncogene Proteins c-etsReceptors, AndrogenSignal TransductionTransforming Growth Factor betaAndrogen AntagonistsAR protein, humanbetaIG-H3 ProteinExtracellular Matrix ProteinsProto-Oncogene Proteins c-etsReceptors, AndrogenSPDEF protein, humanTransforming Growth Factor beta

Identifiers

PMID28811384
OpenAlexW2749149011

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.