Evidence map›Paper›PMID 36428741›Full record

ReviewCancers2022

Preclinical Models of Neuroendocrine Neoplasia.

Andrew J H Sedlack, Kimia Saleh-Anaraki, Suresh Kumar, Po Hien Ear, Kate E Lines, Nitin Roper, Karel Pacak, Emily Bergsland, Dawn E Quelle, James R Howe and 2 more

Abstract readReview
In one paragraph

Review in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. 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

12 authors.

Andrew J H SedlackNational Institute of Biomedical Imaging and Bioengineering, National Institutes of Health (NIH), Bethesda, MD 20892, USA.ORCID 0000-0003-0139-952X
Kimia Saleh-AnarakiNational Cancer Institute, NIH, Bethesda, MD 20892, USA.
Suresh KumarNational Cancer Institute, NIH, Bethesda, MD 20892, USA.
Po Hien EarDepartment of Surgery, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0003-0823-9166
Kate E LinesOxford Center for Diabetes, Endocrinology, and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford OX3 7LE, UK.
Nitin RoperNational Cancer Institute, NIH, Bethesda, MD 20892, USA.ORCID 0000-0002-6514-5468
Karel PacakEunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892, USA.
Emily BergslandUniversity of California, San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, CA 94158, USA.
Dawn E QuelleDepartment of Neuroscience and Pharmacology, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0001-8776-0122
James R HoweDepartment of Surgery, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0001-5312-5972
Yves PommierNational Cancer Institute, NIH, Bethesda, MD 20892, USA.
Jaydira Del RiveroNational Cancer Institute, NIH, Bethesda, MD 20892, USA.ORCID 0000-0001-9710-4030

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Christopher K Laubenthal · 2000 to 2026
$70.0M
Role of RABL6A-PP2A in neuroendocrine tumorsR01CA260200 · NCI · UNIVERSITY OF IOWA · PI NARLA, GOUTHAM, QUELLE, DAWN E · 2021 to 2025
$2.6M
NCI NIH HHS R01 CA260200
6 · The paper itself

Abstract

Neuroendocrine neoplasia (NENs) are a complex and heterogeneous group of cancers that can arise from neuroendocrine tissues throughout the body and differentiate them from other tumors. Their low incidence and high diversity make many of them orphan conditions characterized by a low incidence and few dedicated clinical trials. Study of the molecular and genetic nature of these diseases is limited in comparison to more common cancers and more dependent on preclinical models, including both in vitro models (such as cell lines and 3D models) and in vivo models (such as patient derived xenografts (PDXs) and genetically-engineered mouse models (GEMMs)). While preclinical models do not fully recapitulate the nature of these cancers in patients, they are useful tools in investigation of the basic biology and early-stage investigation for evaluation of treatments for these cancers. We review available preclinical models for each type of NEN and discuss their history as well as their current use and translation.

Indexed as

castration-resistant prostate cancercell linegenetically-engineered mouse modelneuroendocrine tumororganoidsmall cell lung cancerxenograft

Identifiers

PMID36428741
PMCPMC9688518

What OpenQuestion holds

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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.