Evidence map›Paper›PMID 28415823›Full record

ArticleOncotarget2017

Recurrent fusion RNA DUS4L-BCAP29 in non-cancer human tissues and cells.

Yue Tang, Fujun Qin, Aiqun Liu, Hui Li

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed, 39 citations in OpenAlex.

  1. Science advances · 2026
    Article
  2. Review
  3. Overexpression of Chimeric RNA by Retroviral Transduction.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  4. Article
  5. Knockdown of Chimeric RNA by RNAi.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. A Protocol for the Detection of Fusion Transcripts Using RNA-Sequencing Data.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 2 countries.

Yue TangCollege of Life Sciences, Zhengzhou University, Zhengzhou, Henan 450008, P.R. China.
Fujun QinDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Aiqun LiuDepartment of Endoscopy, The Affiliated Tumor Hospital of Guangxi Medical University, Nanning, Guangxi 530021, P.R. China.
Hui LiDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
University of Virginia · USTumor Hospital of Guangxi Medical University · CN

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Thomas P. Loughran · 1987 to 2026
$72.1M
Induction of Gene Fusions by Pre-Existing Chimeric TranscriptsR01CA190713 · NCI · UNIVERSITY OF VIRGINIA · PI LI, HUI · 2014 to 2018
$1.8M
NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA190713
6 · The paper itself

Abstract

Traditional gene fusions are involved in the development of various neoplasia. DUS4L-BCAP29, a chimeric fusion RNA, has been reported to be a cancer-fusion in prostate and gastric cancer, in addition to playing a tumorigenic role. Here, we showed that the DUS4L-BCAP29 fusion transcript exists in a variety of normal tissues. It is also present in non-cancer epithelial, as well as in fibroblast cell lines. Quantitatively, the fusion transcript has a comparable expression in non-cancerous, gastric and prostate cell lines and tissues as in the cancer cell lines and tissues. The loss-of-function approach as previously reported is not sufficient to prove the functionality of the fusion. On the other hand, the gain-of-function approach showed that overexpression of DUS4L-BCAP29 promotes cell growth and motility, even in non-cancer cells. Finally, we provide further evidence that the fusion transcript is a product of cis-splicing between adjacent genes. In summary, we believe that in contrast to traditional gene fusions, DUS4L-BCAP29 cannot be used as a cancer biomarker. Instead, it is a fusion transcript that exists in normal physiology and that its pro-growth effect is not unique to cancer cells.

Indexed as

Gene FusionRNACell LineCell Line, TumorGain of Function MutationGene ExpressionHumansLoss of Function MutationMaleMembrane ProteinsOrgan SpecificityProstatic NeoplasmsSequence Analysis, DNAStomach NeoplasmsTranscription, GeneticBCAP29 protein, humanMembrane ProteinsRNAchimeric RNAcis-SAGeDUS4L-BCAP29fusion transcript

Identifiers

PMID28415823
PMCPMC5458218
OpenAlexW2597005785

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.