Evidence map›Paper›PMID 34681865›Full record

ReviewInternational journal of molecular sciences2021

Parathyroid Tumors: Molecular Signatures.

Francesca Marini, Francesca Giusti, Teresa Iantomasi, Maria Luisa Brandi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Phenotypic Profiling and Molecular Mechanisms in Hyperparathyroidism-jaw Tumor Syndrome.The Journal of clinical endocrinology and metabolism · 2023
    Article
  11. Review
  12. Article
  13. Immunohistochemical Profile of Parathyroid Tumours: A Comprehensive Review.International journal of molecular sciences · 2022
    Review
  14. 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

4 authors at 2 institutions in 1 country.

Francesca MariniDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.ORCID 0000-0002-3678-4922
Francesca GiustiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.ORCID 0000-0002-8576-9606
Teresa IantomasiDepartment of Experimental and Clinical Biomedical Sciences, University of Florence, 50139 Florence, Italy.
Maria Luisa BrandiF.I.R.M.O. Fondazione Italiana Ricerca sulle Malattie dell'Osso (Italian Foundation for the Research on Bone Diseases), 50141 Florence, Italy.ORCID 0000-0002-8741-0592
Fondazione Italiana di Ricerca per la Sclerosi Laterale Amiotrofica · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parathyroid tumors are rare endocrine neoplasms affecting 0.1-0.3% of the general population, including benign parathyroid adenomas (PAs; about 98% of cases), intermediate atypical parathyroid adenomas (aPAs; 1.2-1.3% of cases) and malignant metastatic parathyroid carcinomas (PCs; less than 1% of cases). These tumors are characterized by a variable spectrum of clinical phenotypes and an elevated cellular, histological and molecular heterogeneity that make it difficult to pre-operatively distinguish PAs, aPAs and PCs. Thorough knowledge of genetic, epigenetic, and molecular signatures, which characterize different parathyroid tumor subtypes and drive different tumorigeneses, is a key step to identify potential diagnostic biomarkers able to distinguish among different parathyroid neoplastic types, as well as provide novel therapeutic targets and strategies for these rare neoplasms, which are still a clinical and therapeutic challenge. Here, we review the current knowledge on gene mutations and epigenetic changes that have been associated with the development of different clinical types of parathyroid tumors, both in familial and sporadic forms of these endocrine neoplasms.

Indexed as

MutationAdenomaCyclin-Dependent Kinase Inhibitor p27Epigenesis, GeneticFibromaHumansHyperparathyroidismHyperparathyroidism, PrimaryJaw NeoplasmsMultiple Endocrine Neoplasia Type 1Multiple Endocrine Neoplasia Type 2aParathyroid NeoplasmsProto-Oncogene ProteinsTumor Suppressor ProteinsCDC73 protein, humanCDKN1B protein, humanCyclin-Dependent Kinase Inhibitor p27MEN1 protein, humanProto-Oncogene ProteinsTumor Suppressor Proteinsepigenetic signaturesgene mutationsparathyroid adenomasparathyroid carcinomasparathyroid tumors

Identifiers

PMID34681865
PMCPMC8540444
OpenAlexW3205551390

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.