Evidence map›Paper›PMID 18195709›Full record

ArticleBritish journal of cancer2008

BORIS, a paralogue of the transcription factor, CTCF, is aberrantly expressed in breast tumours.

V D'Arcy, N Pore, F Docquier, Z K Abdullaev, I Chernukhin, G-X Kita, S Rai, M Smart, D Farrar, S Pack and 2 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 104 citations in OpenAlex.

  1. Loss of miR-122 promotes cell migration and poor prognosis in triple-negative breast cancer treated by neoadjuvant chemotherapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  2. Article
  3. Article
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  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
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  13. Article
  14. Article
  15. Article
  16. Targeting CTCFL/BORIS for the immunotherapy of cancer.Cancer immunology, immunotherapy : CII · 2018
    Review
  17. Article
  18. Review
  19. BORIS: a key regulator of cancer stemness.Cancer cell international · 2018
    Review
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

V D'ArcyDepartment of Biological Sciences, University of Essex, Wivenhoe Park, Colchester, Essex CO4 3SQ, UK.
N Pore
F Docquier
Z K Abdullaev
I Chernukhin
G-X Kita
S Rai
M Smart
D Farrar
S Pack
V Lobanenkov
E Klenova
University of Essex · GBNational Institute of Allergy and Infectious Diseases · USQueen Mary University of London · GB

Funding

Regulation of CTCF Functions and Target Sites by Cancer/Testis-specific CTCF Like BORIS FactorZIAAI001021 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LOBANENKOV, VICTOR · 2009 to 2025
$12.7M
Biotechnology and Biological Sciences Research CouncilBreast Cancer Now 2004NOV45Intramural NIH HHSMedical Research Council G0401088Worldwide Cancer Research 99-0514
6 · The paper itself

Abstract

BORIS (for brother of the regulator of imprinted sites), a paralogue of the transcription factor, CTCF, is a novel member of the cancer-testis antigen family. The aims of the present study were as follows: (1) to investigate BORIS expression in breast cells and tumours using immunohistochemical staining, western and real-time RT-PCR analyses and (2) assess potential correlation between BORIS levels in tumours with clinical/pathological parameters. BORIS was detected in all 18 inspected breast cell lines, but not in a primary normal breast cell culture. In 70.7% (41 of 58 cases) BORIS was observed in breast tumours. High levels of BORIS correlated with high levels of progesterone receptor (PR) and oestrogen receptor (ER). The link between BORIS and PR/ER was further confirmed by the ability of BORIS to activate the promoters of the PR and ER genes in the reporter assays. Detection of BORIS in a high proportion of breast cancer patients implies potential practical applications of BORIS as a molecular biomarker of breast cancer. This may be important for diagnosis of the condition and for the therapeutic use of BORIS. The ability of BORIS to activate promoters of the RP and ER genes points towards possible involvement of BORIS in the establishment, progression and maintenance of breast tumours.

Indexed as

Biomarkers, TumorBreastBreast NeoplasmsCell Line, TumorCells, CulturedDNA-Binding ProteinsGene ExpressionHumansImmunohistochemistryPromoter Regions, GeneticReceptors, EstrogenReceptors, ProgesteroneBiomarkers, TumorCTCFL protein, humanDNA-Binding ProteinsReceptors, EstrogenReceptors, Progesterone

Identifiers

PMID18195709
PMCPMC2243163
OpenAlexW2042897749

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.