Evidence map›Paper›PMID 10200298›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Roles of trk family neurotrophin receptors in medullary thyroid carcinoma development and progression.

L M McGregor, B K McCune, J R Graff, P R McDowell, K E Romans, G D Yancopoulos, D W Ball, S B Baylin, B D Nelkin

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

53 citing papers in PubMed, 140 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Activation of TrkB in Parvalbumin interneurons is required for the promotion of reversal learning in spatial and fear memory by antidepressants.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. A novel microRNA located in theThe Journal of biological chemistry · 2017
    Article
  18. Role of Nerve Growth Factor (NGF) and miRNAs in Epithelial Ovarian Cancer.International journal of molecular sciences · 2017
    Review
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

L M McGregorOncology Center, Johns Hopkins Medical Institutions, Baltimore, MD 21231, USA.
B K McCune
J R Graff
P R McDowell
K E Romans
G D Yancopoulos
D W Ball
S B Baylin
B D Nelkin
Johns Hopkins University · USRegeneron (United States) · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007309 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 1985 to 2019
$43.2M
Predoctoral Training Program in Human GeneticsT32GM007814 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VALLE, DAVID · 1985 to 2021
$10.6M
DIFFERENTIATION OF MEDULLARY THYROID CARCINOMA CELLSR01CA047480 · NCI · JOHNS HOPKINS UNIVERSITY · PI NELKIN, BARRY D. · 1988 to 2000
$398k
NCI NIH HHS R01-CA47480NIGMS NIH HHS 2T32GM07814NIGMS NIH HHS GM07309NIGMS NIH HHS T32 GM007309NIGMS NIH HHS T32 GM007814
6 · The paper itself

Abstract

Although initiating mutations in the ret protooncogene have been found in familial and sporadic medullary thyroid carcinoma (MTC), the molecular events underlying subsequent tumor progression stages are unknown. We now report that changes in trk family neurotrophin receptor expression appear to be involved in both preneoplastic thyroid C cell hyperplasia and later tumor progression. Only a subset of normal C cells expresses trk family receptors, but, in C cell hyperplasia, the affected cells consistently express trkB, with variable expression of trkA and trkC. In later stages of gross MTC tumors, trkB expression was substantially reduced, while trkC expression was increased and often intense. In a cell culture model of MTC, exogenous trkB expression resulted in severely impaired tumorigenicity and was associated with 11-fold lower levels of the angiogenesis factor vascular endothelial growth factor. These results suggest that trk family receptor genes participate in MTC development and progression, and, in particular, that trkB may limit MTC tumor growth by inhibition of angiogenesis.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCarcinoma, MedullaryDisease ProgressionFemaleGene Expression RegulationHumansHyperplasiaMiceMice, NudePregnancyProto-Oncogene ProteinsReceptor, Ciliary Neurotrophic FactorReceptor Protein-Tyrosine KinasesReceptors, Nerve Growth FactorReceptor, trkAProto-Oncogene ProteinsReceptor, Ciliary Neurotrophic FactorReceptor Protein-Tyrosine KinasesReceptors, Nerve Growth FactorReceptor, trkAReceptor, trkC

Identifiers

PMID10200298
PMCPMC16368
OpenAlexW2142157691

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.