Evidence map›Paper›PMID 30765319›Full record

ArticleEBioMedicine2019

Serial patient-derived orthotopic xenografting of adenoid cystic carcinomas recapitulates stable expression of phenotypic alterations and innervation.

Ashley Cornett, Harleen K Athwal, Emily Hill, George Murphy, Kenji Yeoh, Christopher A Moskaluk, Robert L Witt, Nisha J D'Silva, Seema Agarwal, Isabelle M A Lombaert

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-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

9 citing papers in PubMed, 16 citations in OpenAlex.

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

10 authors at 4 institutions in 1 country.

Ashley CornettUniversity of Michigan, Biointerfaces Institute, Ann Arbor, MI, United States; University of Michigan, School of Dentistry, Department of Biologic and Materials Sciences, Ann Arbor, MI, United States.
Harleen K AthwalUniversity of Michigan, Biointerfaces Institute, Ann Arbor, MI, United States; University of Michigan, School of Dentistry, Department of Biologic and Materials Sciences, Ann Arbor, MI, United States.
Emily HillUniversity of Michigan, Biointerfaces Institute, Ann Arbor, MI, United States; University of Michigan, School of Dentistry, Department of Biologic and Materials Sciences, Ann Arbor, MI, United States.
George MurphyUniversity of Michigan, Biointerfaces Institute, Ann Arbor, MI, United States; University of Michigan, School of Dentistry, Department of Biologic and Materials Sciences, Ann Arbor, MI, United States.
Kenji YeohUniversity of Michigan, Biointerfaces Institute, Ann Arbor, MI, United States; University of Michigan, School of Dentistry, Department of Biologic and Materials Sciences, Ann Arbor, MI, United States.
Christopher A MoskalukUniversity of Virginia, School of Medicine, Department of Pathology, Charlottesville, VA, United States.
Robert L WittThomas Jefferson University, Department of Otolaryngology-Head and Neck Surgery, Philadelphia, PA, United States.
Nisha J D'SilvaUniversity of Michigan, School of Dentistry, Department of Periodontics and Oral Medicine, Ann Arbor, MI, United States; University of Michigan, Medical School, Department of Pathology, Ann Arbor, MI, United States.
Seema AgarwalGeorgetown University Medical Center, Department of Pathology, Center for Cell Reprogramming, Washington, DC, United States.
Isabelle M A LombaertUniversity of Michigan, Biointerfaces Institute, Ann Arbor, MI, United States; University of Michigan, School of Dentistry, Department of Biologic and Materials Sciences, Ann Arbor, MI, United States. Electronic address: lombaert@umich.edu.
University of Michigan · USGeorgetown University · USThomas Jefferson University · USUniversity of Virginia · US

Funding

Improving Survival in Oral Cancer by Disruption of Tumor ProgressionR35DE027551 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI D'SILVA, NISHA J · 2017 to 2024
$8.1M
Manipulating Stem Cells to Provide Long Term Regeneration of Irradiated Salivary GlandsR01DE027034 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOMBAERT, ISABELLE M.A. · 2018 to 2022
$1.8M
Identifying stem cells for future salivary gland stem cell therapyR00DE022557 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOMBAERT, ISABELLE M.A. · 2015 to 2017
$741k
NIDCR NIH HHS R00 DE022557NIDCR NIH HHS R01 DE027034NIDCR NIH HHS R35 DE027551
6 · The paper itself

Abstract

backgroundPatient-derived xenograft (PDX) models have significantly enhanced cancer research, and often serve as a robust model. However, enhanced growth rate and altered pathological phenotype with serial passages have repeatedly been shown in adenoid cystic carcinoma (ACC) PDX tumors, which is a major concern.

methodsWe evaluated the fidelity of ACCs in their natural habitat by performing ACC orthotopic xenotransplantation (PDOX) in salivary glands.

findingsOur PDOX model enabled solid tumors to integrate within the local epithelial, stromal and neuronal environment. Over serial passages, PDOX tumors maintained their stereotypic MYB-NFIB translocation, and FGFR2 and ATM point mutations. Tumor growth rate and histopathology were retained, including ACCs hallmark presentations of cribriform, tubular, solid areas and innervation. We also demonstrate that the PDOX model retains its capacity as a tool for drug testing.

interpretationUnlike the precedent PDX model, our data shows that the PDOX is a superior model for future cancer biology and therapy research. FUND: This work was supported by the National Institutes of Health (NIH)/National Institute of Dental and Craniofacial Research (NIDCR) grants DE022557, DE027034, and DE027551.

Indexed as

PhenotypeAnimalsAtaxia Telangiectasia Mutated ProteinsCarcinoma, Adenoid CysticHead and Neck NeoplasmsHumansMiceOncogene Proteins, FusionPoint MutationReceptor, Fibroblast Growth Factor, Type 2Salivary GlandsXenograft Model Antitumor AssaysAtaxia Telangiectasia Mutated ProteinsATM protein, humanFGFR2 protein, humanMYB-NFIB fusion protein, humanOncogene Proteins, FusionReceptor, Fibroblast Growth Factor, Type 2Adenoid cystic carcinomaDrug treatmentFidelityNeural invasionOrthotopic PDX modelSalivary gland

Identifiers

PMID30765319
PMCPMC6442226
OpenAlexW2913434140

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.