Evidence map›Paper›PMID 25279549›Full record

ArticlePloS one2014

High expression of hTERT and stemness genes in BORIS/CTCFL positive cells isolated from embryonic cancer cells.

Loredana Alberti, Stéphanie Renaud, Lorena Losi, Serge Leyvraz, Jean Benhattar

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 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
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

18 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. CTCF and CTCFL in cancer.Current opinion in genetics & development · 2020
    Review
  5. Review
  6. Molecular cancer research : MCR · 2019
    Article
  7. Article
  8. Article
  9. Targeting CTCFL/BORIS for the immunotherapy of cancer.Cancer immunology, immunotherapy : CII · 2018
    Review
  10. Article
  11. Article
  12. BORIS: a key regulator of cancer stemness.Cancer cell international · 2018
    Review
  13. Article
  14. Observational
  15. Sperm-associated antigen 9 (SPAG9) promotes the survival and tumor growth of triple-negative breast cancer cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  16. Article
  17. Article
  18. 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

5 authors at 2 institutions in 2 countries.

Loredana AlbertiInstitute of Pathology, Lausanne University Hospital, Lausanne, Switzerland.
Stéphanie RenaudInstitute of Biotechnology, University of Lausanne, Lausanne, Switzerland.
Lorena LosiDepartment of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Serge LeyvrazDepartment of Oncology, Lausanne University Hospital, Lausanne, Switzerland.
Jean BenhattarInstitute of Pathology, Lausanne University Hospital, Lausanne, Switzerland; Biopath Lab, Lausanne, Switzerland.
University of Lausanne · CHUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BORIS/CTCFL is a member of cancer testis antigen family normally expressed in germ cells. In tumors, it is aberrantly expressed although its functions are not completely well-defined. To better understand the functions of BORIS in cancer, we selected the embryonic cancer cells as a model. Using a molecular beacon, which specifically targets BORIS mRNA, we demonstrated that BORIS positive cells are a small subpopulation of tumor cells (3-5% of total). The BORIS-positive cells isolated using BORIS-molecular beacon, expressed higher telomerase hTERT, stem cell (NANOG, OCT4, SOX2) and cancer stem cell marker genes (CD44 and ALDH1) compared to the BORIS-negative tumor cells. In order to define the functional role of BORIS, stable BORIS-depleted embryonic cancer cells were generated. BORIS silencing strongly down-regulated the expression of hTERT, stem cell and cancer stem cell marker genes. Moreover, the BORIS knockdown increased cellular senescence in embryonic cancer cells, revealing a putative role of BORIS in the senescence biological program. Our data indicate an association of BORIS expressing cells subpopulation with the expression of stemness genes, highlighting the critical role played by BORIS in embryonic neoplastic disease.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBlotting, WesternCell ProliferationDNA-Binding ProteinsDNA MethylationEmbryonic Stem CellsEpigenesis, GeneticFemaleHumansMolecular ImagingNeoplastic Stem CellsOvarian NeoplasmsPromoter Regions, GeneticReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionCTCFL protein, humanDNA-Binding ProteinsRNA, MessengerRNA, Small InterferingTelomeraseTERT protein, human

Identifiers

PMID25279549
PMCPMC4184884
OpenAlexW2142922561

What OpenQuestion holds

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LicenceCC BY
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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.