Evidence map›Paper›PMID 12841847›Full record

ArticleThe Biochemical journal2003

The POU homeodomain protein OCT3 as a potential transcriptional activator for fibroblast growth factor-4 (FGF-4) in human breast cancer cells.

Peixiang Wang, Donald R Branch, Meenakshi Bali, Gilbert A Schultz, Paul E Goss, Tianru Jin

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2003. 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
1.1field-weighted citation impact, top 24% 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, 63 citations in OpenAlex.

  1. Article
  2. Article
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  5. Distinctive expression pattern of OCT4 variants in different types of breast cancer.Cancer biomarkers : section A of Disease markers · 2017
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  7. Review
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  10. Fluorouracil selectively enriches stem-like cells in the lung adenocarcinoma cell line SPC.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Article
  11. Octamer-binding transcription factors: genomics and functions.Frontiers in bioscience (Landmark edition) · 2013
    Review
  12. Article
  13. Review
  14. Differential expression profiling between atypical teratoid/rhabdoid and medulloblastoma tumor in vitro and in vivo using microarray analysis.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2010
    Article
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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

6 authors at 3 institutions in 1 country.

Peixiang WangDepartment of Medicine, University of Toronto, 67 College Street, Toronto, ON, Canada M5G 2M1.
Donald R Branch
Meenakshi Bali
Gilbert A Schultz
Paul E Goss
Tianru Jin
University of Toronto · CAUniversity Health Network · CAUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The POU (representing a homeodomain protein family of which the founder members are Pit-1, Oct-1/2 and Unc-86) homeodomain protein OCT3/Oct-3 (where OCT stands for octamer-binding protein) is an embryonic transcription factor expressed in oocytes, embryonic stem and embryonic carcinoma cells. We have demonstrated previously that human breast cancer cells regain the ability to express OCT3 mRNA [Jin, Branch, Zhang, Qi, Youngson and Goss (1999) Int. J. Cancer 81, 104-112]. Antibodies against human OCT3 were not available when this study was conducted. By using a human OCT3-glutathione S-transferase fusion protein to affinity purify a polyclonal antibody against the mouse Oct-3, we obtained an antibody that enabled us to detect OCT3 in human breast cancer cells by Western-blot analysis. Thus we have now confirmed that OCT3 is expressed in human breast cancer cells but not in normal human breasts and in three other organs. When breast cancer cell lines were treated with all- trans -retinoic acid, OCT3 expression was repressed, associated with decreased cell proliferation. Although another POU protein Brn-3 has been shown to be a repressor for BRCA1 (breast-cancer susceptibility gene 1), OCT3 does not repress human or mouse BRCA1/Brca-1 promoters. However, OCT3 is capable of activating a fusion promoter containing the fibroblast growth factor-4 (FGF-4) enhancer element. In addition, we documented for the first time that human breast cancer cells express FGF-4 protein, and its expression could be inhibited by all- trans -retinoic acid. Furthermore, overexpressing OCT3 stimulated endogenous FGF-4 expression in MCF7 breast cancer cell line. These observations indicate that OCT3 protein is selectively expressed in human breast cancer cells, and its expression may be implicated in mammary gland tumorigenesis via up-regulating FGF-4 expression.

Indexed as

Gene Expression Regulation, NeoplasticTranscriptional ActivationAntineoplastic AgentsBlotting, WesternBreast NeoplasmsCell LineDNA-Binding ProteinsDown-RegulationFemaleFibroblast Growth Factor 4Fibroblast Growth FactorsHumansOctamer Transcription Factor-3Promoter Regions, GeneticProto-Oncogene ProteinsResponse ElementsAntineoplastic AgentsDNA-Binding ProteinsFGF4 protein, humanFibroblast Growth Factor 4Fibroblast Growth FactorsOctamer Transcription Factor-3POU5F1 protein, humanProto-Oncogene ProteinsThymidine KinaseTranscription FactorsTretinoin

Identifiers

PMID12841847
PMCPMC1223663
OpenAlexW2009383189

What OpenQuestion holds

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Registered trials

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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.