Evidence map›Paper›PMID 37082125›Full record

ArticleFrontiers in endocrinology2023

Long-term organoid culture of a small intestinal neuroendocrine tumor.

Sabrina D'Agosto, Elena Fiorini, Francesco Pezzini, Pietro Delfino, Michele Simbolo, Caterina Vicentini, Silvia Andreani, Paola Capelli, Borislav Rusev, Rita T Lawlor and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Multifaceted modeling of small intestinal neuroendocrine tumors.Endocrine oncology (Bristol, England) · 2024
    Review
  3. Review
  4. Review
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

16 authors at 2 institutions in 1 country.

Sabrina D'AgostoDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
Elena FioriniDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
Francesco PezziniDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
Pietro DelfinoDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
Michele SimboloDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
Caterina VicentiniCentre for Applied Research on Cancer (ARC-Net) Research Centre, University of Verona, Verona, Italy.
Silvia AndreaniCentre for Applied Research on Cancer (ARC-Net) Research Centre, University of Verona, Verona, Italy.
Paola CapelliAzienda Ospedaliera Integrata dell'Università di Verona, Verona, Italy.
Borislav RusevCentre for Applied Research on Cancer (ARC-Net) Research Centre, University of Verona, Verona, Italy.
Rita T LawlorCentre for Applied Research on Cancer (ARC-Net) Research Centre, University of Verona, Verona, Italy.
Claudio BassiPancreas Institute, Department of Surgery, University and Hospital Trust of Verona, Verona, Italy.
Luca LandoniPancreas Institute, Department of Surgery, University and Hospital Trust of Verona, Verona, Italy.
Antonio PeaPancreas Institute, Department of Surgery, University and Hospital Trust of Verona, Verona, Italy.
Claudio LuchiniDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
Aldo ScarpaDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
Vincenzo CorboDepartment of Diagnostics and Public Health, University of Verona, Verona, Italy.
University of Verona · ITAzienda Ospedaliera Universitaria Integrata Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are rare and highly heterogeneous neoplasms whose incidence has markedly increased over the last decades. A grading system based on the tumor cells' proliferation index predicts high-risk for G3 NETs. However, low-to-intermediate grade (G1/G2) NETs have an unpredictable clinical course that varies from indolent to highly malignant. Cultures of human cancer cells enable to perform functional perturbation analyses that are instrumental to enhance our understanding of cancer biology. To date, no tractable and reliable long-term culture of G1/G2 NET has been reported to permit disease modeling and pharmacological screens. Here, we report of the first long-term culture of a G2 metastatic small intestinal NET that preserves the main genetic drivers of the tumor and retains expression patterns of the endocrine cell lineage. Replicating the tissue, this long-term culture showed a low proliferation index, and yet it could be propagated continuously without dramatic changes in the karyotype. The model was readily available for pharmacological screens using targeted agents and as expected, showed low tumorigenic capacity

Indexed as

Neuroendocrine TumorsHumansIntestinal NeoplasmsKi-67 AntigenNeoplasm GradingPancreatic NeoplasmsPrognosisReceptor Protein-Tyrosine KinasesStomach NeoplasmsKi-67 AntigenReceptor Protein-Tyrosine Kinases3D cultureneuroendocrine tumororganoidspreclinical modelsmall intestinal tumor

Identifiers

PMID37082125
PMCPMC10112019
OpenAlexW4362553822

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.