Evidence map›Paper›PMID 28214592›Full record

ArticleMolecular and cellular endocrinology2017

Role of a p53 polymorphism in the development of nonfunctional pituitary adenomas.

Garima Yagnik, Arman Jahangiri, Rebecca Chen, Jeffrey R Wagner, Manish K Aghi

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. The hallmarks of cancer… in pituitary tumors?Reviews in endocrine & metabolic disorders · 2023
    Review
  4. Article
  5. Article
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  7. Review
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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

5 authors at 1 institution in 1 country.

Garima YagnikUniversity of California, San Francisco (UCSF) Department of Neurological Surgery and Brain Tumor Research Center, 1450 Third Street Room HD-465, San Francisco, CA 94158, USA. Electronic address: Garima.Yagnik@ucsf.edu.
Arman JahangiriUniversity of California, San Francisco (UCSF) Department of Neurological Surgery and Brain Tumor Research Center, 1450 Third Street Room HD-465, San Francisco, CA 94158, USA.
Rebecca ChenUniversity of California, San Francisco (UCSF) Department of Neurological Surgery and Brain Tumor Research Center, 1450 Third Street Room HD-465, San Francisco, CA 94158, USA.
Jeffrey R WagnerUniversity of California, San Francisco (UCSF) Department of Neurological Surgery and Brain Tumor Research Center, 1450 Third Street Room HD-465, San Francisco, CA 94158, USA.
Manish K AghiUniversity of California, San Francisco (UCSF) Department of Neurological Surgery and Brain Tumor Research Center, 1450 Third Street Room HD-465, San Francisco, CA 94158, USA. Electronic address: Manish.Aghi@ucsf.edu.
University of California, San Francisco · US

Funding

Training Program in Translational Brain Tumor ResearchT32CA151022 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2010 to 2026
$6.6M
Tumor cell and microenvironment changes causing antiangiogenic therapy resistanceR01NS079697 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AGHI, MANISH · 2013 to 2021
$3.2M
NCI NIH HHS T32 CA151022NINDS NIH HHS R01 NS079697
6 · The paper itself

Abstract

Non-functional pituitary adenomas (NFPAs) are among the commonest intracranial neoplasms. While histologically benign, NFPAs sometimes become large enough to limit therapeutic options and reduce quality of life. Investigations of the molecular etiology of NFPAs have failed to identify prevalent genetic changes and, while a role for p53 has been suggested, TP53 gene alterations have yet to be described in NFPAs. We found that the polymorphism rs1042522:C > G in codon 72 of exon 4 of the TP53 gene, whose C variant produces a proline and is more common in most ethnicities, has a G variant producing an arginine in 79.8% of NFPAs (n = 42; p < 1.411 × 10

Indexed as

Genetic Predisposition to DiseaseAdenomaCase-Control StudiesCell ProliferationHumansNeoplasm InvasivenessNeovascularization, PathologicOdds RatioPituitary NeoplasmsPolymorphism, Single NucleotideTranscription, GeneticTumor Suppressor Protein p53Tumor Suppressor Protein p53p53Pituitary adenomaPolymorphism

Identifiers

PMID28214592
PMCPMC5553295
OpenAlexW2588709043

What OpenQuestion holds

Textmetadata
LicenceTDM
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.