Evidence map›Paper›PMID 26077989›Full record

ArticleBMC cancer2015

TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survival.

Lucia Micale, Carmela Fusco, Andrea Fontana, Raffaela Barbano, Bartolomeo Augello, Pasquelena De Nittis, Massimiliano Copetti, Maria Teresa Pellico, Barbara Mandriani, Dario Cocciadiferro and 8 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

36 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Rise of TRIM8: A Molecule of Duality.Molecular therapy. Nucleic acids · 2020
    Review
  18. Review
  19. Article
  20. 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

18 authors at 1 institution in 1 country.

Lucia MicaleMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. l.micale@operapadrepio.it.
Carmela FuscoMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. c.fusco@operapadrepio.it.
Andrea FontanaBiostatistics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. a.fontana@operapadrepio.it.
Raffaela BarbanoLaboratory of Oncology, IRCCS Casa Sollievo della Sofferenza, I-71013, San Giovanni Rotondo (FG), Italy. r.barbano@operapadrepio.it.
Bartolomeo AugelloMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. bartolomeoaugello@gmail.com.
Pasquelena De NittisMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. elena.denittis@libero.it.
Massimiliano CopettiBiostatistics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. m.copetti@operapadrepio.it.
Maria Teresa PellicoMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. mt.pellico@operapadrepio.it.
Barbara MandrianiMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. bmandriani@gmail.com.
Dario CocciadiferroMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. dariococciadiferro@gmail.com.
Paola ParrellaLaboratory of Oncology, IRCCS Casa Sollievo della Sofferenza, I-71013, San Giovanni Rotondo (FG), Italy. pparrella@operapadrepio.it.
Vito Michele FazioLaboratory of Oncology, IRCCS Casa Sollievo della Sofferenza, I-71013, San Giovanni Rotondo (FG), Italy. fazio@unicampus.it.
Lucia Maria Cecilia DimitriPathology Unit, IRCCS Casa Sollievo della Sofferenza, I-71013, San Giovanni Rotondo (FG), Italy. l.dimitri@operapadrepio.it.
Vincenzo D'AngeloNeurosurgery Unit, IRCCS Casa Sollievo Della Sofferenza, San Giovanni Rotondo (FG), Italy. v.dangelo@operapadrepio.it.
Chiara NovielliMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy. chiara.novielli@unimi.it.
Lidia LarizzaMedical Genetics, Department of Health Sciences, Università degli Studi di Milano, Milan, Italy. lidia.larizza@unimi.it.
Antonio DagaGene Transfer Lab; IRCSS Azienda Ospedaliera Universitaria San Martino-IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy. antonio.daga@istge.it.
Giuseppe MerlaMedical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, Poliambulatorio Giovanni Paolo II, I-71013, San Giovanni Rotondo (FG), Italy. g.merla@operapadrepio.it.
Istituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman gliomas are a heterogeneous group of primary malignant brain tumors whose molecular pathogenesis is not yet solved. In this regard, a major research effort has been directed at identifying novel specific glioma-associated genes. Here, we investigated the effect of TRIM8 gene in glioma.

methodsTRIM8 transcriptional level was profiled in our own glioma cases collection by qPCR and confirmed in the independent TCGA glioma cohort. The association between TRIM8 expression and Overall Survival and Progression-free Survival in TCGA cohort was determined by using uni-multivariable Cox regression analysis. The effect of TRIM8 on patient glioma cell proliferation was evaluated by performing MTT and clonogenic assays. The mechanisms causing the reduction of TRIM8 expression were explored by using qPCR and in vitro assays.

resultsWe showed that TRIM8 expression correlates with unfavorable clinical outcome in glioma patients. We found that a restored TRIM8 expression induced a significant reduction of clonogenic potential in U87MG and patient's glioblastoma cells. Finally we provide experimental evidences showing that miR-17 directly targets the 3' UTR of TRIM8 and post-transcriptionally represses the expression of TRIM8.

conclusionsOur study provides evidences that TRIM8 may participate in the carcinogenesis and progression of glioma and that the transcriptional repression of TRIM8 might have potential value for predicting poor prognosis in glioma patients.

Indexed as

PrognosisBrain NeoplasmsCarrier ProteinsCell ProliferationDisease-Free SurvivalFemaleGene Expression Regulation, NeoplasticGliomaHumansKaplan-Meier EstimateMaleNeoplasm GradingNerve Tissue ProteinsCarrier ProteinsNerve Tissue ProteinsTRIM8 protein, human

Identifiers

PMID26077989
PMCPMC4468980
OpenAlexW2118070760

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.