Evidence map›Paper›PMID 35082382›Full record

ArticleOncogene2022

SELENOF is a new tumor suppressor in breast cancer.

Alexandra Zigrossi, Lenny K Hong, Roudy C Ekyalongo, Cindy Cruz-Alvarez, Emily Gornick, Alan M Diamond, Irida Kastrati

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Selenium-Containing Compounds in Breast Cancer Therapy.Biological trace element research · 2026
    Review
  3. Article
  4. Review
  5. Animals : an open access journal from MDPI · 2026
    Article
  6. Article
  7. Article
  8. The selenium paradox friend or foe in breast cancer?Annals of medicine and surgery (2012) · 2025
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Selenium status and type 2 diabetes risk.Archives of biochemistry and biophysics · 2022
    Review
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 2 institutions in 1 country.

Alexandra ZigrossiDepartment of Cancer Biology, Loyola University Chicago, Maywood, IL, 60153, USA.
Lenny K HongDepartment of Pathology, University of Illinois at Chicago, Chicago, IL, 60612, USA.
Roudy C EkyalongoDepartment of Cancer Biology, Loyola University Chicago, Maywood, IL, 60153, USA.
Cindy Cruz-AlvarezDepartment of Cancer Biology, Loyola University Chicago, Maywood, IL, 60153, USA.
Emily GornickDepartment of Cancer Biology, Loyola University Chicago, Maywood, IL, 60153, USA.
Alan M DiamondDepartment of Pathology, University of Illinois at Chicago, Chicago, IL, 60612, USA.
Irida KastratiDepartment of Cancer Biology, Loyola University Chicago, Maywood, IL, 60153, USA. ikastrati@luc.edu.ORCID http://orcid.org/0000-0002-8086-1411
Loyola University Chicago · USUniversity of Illinois Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidemiological evidence has indicated an inverse association between selenium status and various types of cancer, including breast cancer. Selenoproteins are the primary mediators of selenium effects in human health. We have previously reported loss of heterozygosity in breast tumor samples of the gene for one of the selenoproteins, SELENOF. The function of SELENOF remains unclear and whether SELENOF levels impact breast cancer risk or outcome is unknown. The mining of breast cancer patient databases revealed that SELENOF mRNA is significantly lower in late-stage tumor samples and lower levels of SELENOF also predict poor patient outcome from breast cancer. Genetically manipulating SELENOF in human breast cancer cells or in the murine mammary gland by overexpression, silencing or knockout impacted cell viability by affecting both proliferation and cell death. Restoring SELENOF can attenuate a number of aggressive cancer phenotypes in breast cancer cells, including clonogenic survival, and enhance the response to drugs or radiation used in breast cancer therapy. Importantly, enhancing SELENOF expression reduced in vivo tumor growth in a murine xenograft model of breast cancer. These data indicate that SELENOF is a new tumor suppressor in breast cancer.

Indexed as

Breast NeoplasmsSelenoproteinsAnimalsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansMiceTumor Suppressor ProteinsSELENOF protein, humanSelenoproteinsTumor Suppressor Proteins

Identifiers

PMID35082382
OpenAlexW4210249675

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.