Evidence map›Paper›PMID 16299399›Full record

ReviewEndocrine pathology2005

Alterations of the BRAF gene in thyroid tumors.

Raffaele Ciampi, Yuri E Nikiforov

Abstract readReview
PubMed Publisher
In one paragraph

Review in Endocrine pathology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 113 citations in OpenAlex.

  1. Review
  2. Follicular cell-derived thyroid carcinomas harboring novel geneticArchives of endocrinology and metabolism · 2024
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. DNA methylation alterations as therapeutic prospects in thyroid cancer.Journal of endocrinological investigation · 2019
    Review
  13. Review
  14. Review
  15. Oncogenesis of Thyroid CancerAsian Pacific journal of cancer prevention : APJCP · 2017
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Frequent BRAF gain in low-grade diffuse gliomas with 1p/19q loss.Brain pathology (Zurich, Switzerland) · 2012
    Article
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

2 authors at 1 institution in 1 country.

Raffaele CiampiDepartment of Pathology and Laboratory Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267-0529, USA.
Yuri E Nikiforov
University of Cincinnati Medical Center · US

Funding

Mechanisms of RET/PTC rearrangements in thyroid cancerR01CA088041 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIKIFOROV, YURI E · 2001 to 2017
$3.8M
NCI NIH HHS R01CA88041
6 · The paper itself

Abstract

BRAF belongs to the RAF family of protein kinases that are important components of the MAPK signaling pathway mediating cell growth, differentiation and survival. Activating point mutation of the BRAF gene resulting in V600E (previously designated as V599E) is a common event in thyroid papillary carcinoma, being found in approx 40% of this tumor. It has strong association with classical papillary carcinoma and tall cell and possibly Warthin-like variants. This mutation also occurs in thyroid poorly differentiated and anaplastic carcinomas, usually those containing areas of papillary carcinoma. Alterations in the BRAF gene do not overlap with RAS mutations and RET/PTC rearrangement, indicating that activation of one of the effectors of the MAPK pathway is sufficient for papillary thyroid carcinogenesis. Recently, another mechanism of BRAF activation has been identified, which involves chromosome 7q inversion that results in the AKAP9-BRAF fusion. It is rare in sporadic papillary carcinomas and is more common in tumors associated with radiation exposure. Yet another mechanism of BRAF activation may involve copy number gain, which is seen in a significant portion of thyroid follicular tumors of both conventional and oncocytic (Hürthle cell) types.

Indexed as

Point MutationAdaptor Proteins, Signal TransducingAdultA Kinase Anchor ProteinsCarcinoma, PapillaryCytoskeletal ProteinsGene DosageGene FusionGene RearrangementHumansMiddle AgedNeoplasm StagingProto-Oncogene Proteins B-rafThyroid NeoplasmsAdaptor Proteins, Signal TransducingAKAP9 protein, humanA Kinase Anchor ProteinsBRAF protein, humanCytoskeletal ProteinsProto-Oncogene Proteins B-raf

Identifiers

PMID16299399
OpenAlexW2046468922

What OpenQuestion holds

Textmetadata
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.