Evidence map›Paper›PMID 23662285›Full record

ReviewBioMed research international2013

From notochord formation to hereditary chordoma: the many roles of Brachyury.

Yutaka Nibu, Diana S José-Edwards, Anna Di Gregorio

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
8.1field-weighted citation impact, top 2% 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, 92 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Extra-Axial Soft Tissue Chordoma of Hand: A Rare Case Report.Journal of orthopaedic case reports · 2025
    Article
  5. Review
  6. Article
  7. A rare posterior mediastinal mass: chordoma.Journal of surgical case reports · 2024
    Article
  8. Chordoma: demographics and survival analysis with a focus on racial disparities and the role of surgery, a U.S. population-based study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Frontiers in molecular biosciences · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Skull base chordomas review of current treatment paradigms.World journal of otorhinolaryngology - head and neck surgery · 2020
    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

3 authors at 1 institution in 1 country.

Yutaka NibuDepartment of Cell and Developmental Biology, Weill Medical College of Cornell University, New York, NY 10065, USA. yun2001@med.cornell.edu
Diana S José-Edwards
Anna Di Gregorio
Cornell University · US

Funding

TRAINING PROGRAM IN MOLECULAR AND CELLULAR BIOLOGYT32GM008539 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BROWN, ANTHONY M.C. · 1995 to 2020
$5.0M
Brachyury-downstream gene networks in the notochordR01HD050704 · NICHD · WEILL MEDICAL COLL OF CORNELL UNIV · PI DI GREGORIO, ANNA · 2006 to 2010
$1.8M
Brachyury-downstream gene networks in the notochordR01GM100466 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI DI GREGORIO, ANNA · 2012 to 2015
$1.4M
NICHD NIH HHS R01 HD050704NICHD NIH HHS R01HD050704-05S1NIGMS NIH HHS GM100466NIGMS NIH HHS R01 GM100466NIGMS NIH HHS T32 GM008539
6 · The paper itself

Abstract

Chordoma is a rare, but often malignant, bone cancer that preferentially affects the axial skeleton and the skull base. These tumors are both sporadic and hereditary and appear to occur more frequently after the fourth decade of life; however, modern technologies have increased the detection of pediatric chordomas. Chordomas originate from remnants of the notochord, the main embryonic axial structure that precedes the backbone, and share with notochord cells both histological features and the expression of characteristic genes. One such gene is Brachyury, which encodes for a sequence-specific transcription factor. Known for decades as a main regulator of notochord formation, Brachyury has recently gained interest as a biomarker and causative agent of chordoma, and therefore as a promising therapeutic target. Here, we review the main characteristics of chordoma, the molecular markers, and the clinical approaches currently available for the early detection and possible treatment of this cancer. In particular, we report on the current knowledge of the role of Brachyury and of its possible mechanisms of action in both notochord formation and chordoma etiogenesis.

Indexed as

Brachyury ProteinCarcinogenesisChordomaFetal ProteinsGene DosageHumansNotochordT-Box Domain ProteinsTranscription, GeneticBrachyury ProteinFetal ProteinsT-Box Domain Proteins

Identifiers

PMID23662285
PMCPMC3626178
OpenAlexW1975382013

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.