Evidence map›Paper›PMID 33459926›Full record

ReviewEndocrine pathology2021

Molecular Pathology of Well-Differentiated Gastro-entero-pancreatic Neuroendocrine Tumors.

Sylvia L Asa, Stefano La Rosa, Olca Basturk, Volkan Adsay, Marianna Minnetti, Ashley B Grossman

Abstract readReview
PubMed Publisher
In one paragraph

Review in Endocrine pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. [Multiple neuroendocrine tumors of the pancreas].Pathologie (Heidelberg, Germany) · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Pancreatoblastomas and mixed and pure acinar cell carcinomas share epigenetic signatures distinct from other neoplasms of the pancreas.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. 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

6 authors at 6 institutions in 5 countries.

Sylvia L AsaDepartment of Pathology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH, USA. pathlady01@gmail.com.ORCID http://orcid.org/0000-0001-8418-5054
Stefano La RosaInstitute of Pathology, University Hospital and University of Lausanne, Lausanne, Switzerland.
Olca BasturkDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Volkan AdsayDepartment of Pathology and Research Center for Translational Medicine (KUTTAM), Koç University Hospital, Istanbul, Turkey.
Marianna MinnettiDepartment of Experimental Medicine, Sapienza University of Rome, Rome, Italy.
Ashley B GrossmanGreen Templeton College, University of Oxford and ENETS Centre of Excellence, Royal Free Hospital, London, UK.
Koç University · TRMemorial Sloan Kettering Cancer Center · USSapienza University of Rome · ITThe Royal Free Hospital · GBUniversity Hospitals of Cleveland · USUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Well differentiated neuroendocrine tumors (NETs) arising in the gastrointestinal and pancreaticobiliary system are the most common neuroendocrine neoplasms. Studies of the molecular basis of these lesions have identified genetic mutations that predispose to familial endocrine neoplasia syndromes and occur both as germline events and in sporadic tumors. The mutations often involve epigenetic regulators rather than the oncogenes and tumor suppressors that are affected in other malignancies. Somatic copy number alterations and miRNAs have also been implicated in the development and progression of some of these tumors. The molecular profiles differ by location, but many are shared by tumors in other sites, including those outside the gastroenteropancreatic system. The approach to therapy relies on both the neuroendocrine nature of these tumors and the identification of specific alterations that can serve as targets for precision oncologic approaches.

Indexed as

Gastrointestinal NeoplasmsHumansNeuroendocrine TumorsOncogenesPancreatic NeoplasmsPathology, MolecularStomach NeoplasmsGastrointestinalHepatobiliaryMolecularNeuroendocrine tumorPancreatic

Identifiers

PMID33459926
OpenAlexW3124388336

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.