Evidence map›Paper›PMID 30238687›Full record

ArticleCancer science2018

Androgen-responsive tripartite motif 36 enhances tumor-suppressive effect by regulating apoptosis-related pathway in prostate cancer.

Naoki Kimura, Yuta Yamada, Ken-Ichi Takayama, Tetsuya Fujimura, Satoru Takahashi, Haruki Kume, Satoshi Inoue

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
  2. Article
  3. Multifaceted role ofMedComm · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Extracellular Polysaccharide fromJournal of clinical and translational hepatology · 2022
    Article
  10. The TRIM proteins in cancer: from expression to emerging regulatory mechanisms.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. The Expression of Tripartite Motif Protein 36 andGastroenterology research and practice · 2020
    Article
  15. Review
  16. TRIM proteins in neuroblastoma.Bioscience reports · 2019
    Review
  17. Review
  18. Article
  19. 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

7 authors at 5 institutions in 1 country.

Naoki KimuraDepartment of Functional Biogerontology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Yuta YamadaDepartment of Urology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Ken-Ichi TakayamaDepartment of Functional Biogerontology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Tetsuya FujimuraDepartment of Urology, Jichi Medical University, Tochigi, Japan.
Satoru TakahashiDepartment of Urology, Nihon University School of Medicine, Tokyo, Japan.
Haruki KumeDepartment of Urology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Satoshi InoueDepartment of Functional Biogerontology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.ORCID http://orcid.org/0000-0003-1247-3844
Tokyo Metropolitan Institute of Gerontology · JPFukuoka Tokushukai Hospital · JPJichi Medical University · JPNihon University · JPThe University of Tokyo · JP

Funding

Japan Agency for Medical Research and Development P-CREATEJapan Society for the Promotion of Science 15K15353Japan Society for the Promotion of Science 15K15581Japan Society for the Promotion of Science 17H04334Takeda Science Foundation
6 · The paper itself

Abstract

Tripartite motif 36 (TRIM36) belongs to the TRIM family, most members of which are involved in ubiquitination and degradation of target proteins by functioning as E3 ubiquitin ligases. The function of TRIM36 has not been well documented, therefore, we investigated the clinical significance and function of TRIM36 in human prostate cancer (PC). Multivariate logistic regression analysis showed that TRIM36 immunoreactivity was an independent predictor of cancer-specific survival of PC patients. Gain-of-function study revealed that overexpression of TRIM36 suppressed cell proliferation and migration of LNCaP, 22Rv1, and DU145 cells. Moreover, TRIM36 knockdown using siRNA suppressed apoptosis and promoted cell proliferation and migration in LNCaP and 22Rv1 cells. Furthermore, our microarray analysis revealed that the apoptosis-related pathway was significantly upregulated by TRIM36 overexpression. The TUNEL assay showed that apoptosis promoted by docetaxel treatment was alleviated in siTRIM36-treated LNCaP and 22Rv1 cells. Taken together, these results suggest that high expression of TRIM36 is associated with favorable prognosis and that TRIM36 plays a tumor-suppressive role by inhibiting cell proliferation and migration as well as promoting apoptosis in PC.

Indexed as

Apoptosis Regulatory ProteinsCarrier ProteinsCell Line, TumorCell MovementCell ProliferationCell SurvivalGene Expression Regulation, NeoplasticHumansMaleNeoplasm GradingOligonucleotide Array Sequence AnalysisPrognosisProgression-Free SurvivalProstatic NeoplasmsSignal TransductionTripartite Motif ProteinsApoptosis Regulatory ProteinsCarrier ProteinsTRIM36 protein, humanTripartite Motif ProteinsUbiquitin-Protein Ligasesimmunohistochemistrymicroarrayprostate cancerTRIM familytripartite motif

Identifiers

PMID30238687
PMCPMC6272107
OpenAlexW2889926123

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.