Evidence map›Paper›PMID 37703185›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2024

Osteosarcoma PDX-Derived Cell Line Models for Preclinical Drug Evaluation Demonstrate Metastasis Inhibition by Dinaciclib through a Genome-Targeted Approach.

Courtney R Schott, Amanda L Koehne, Leanne C Sayles, Elizabeth P Young, Cuyler Luck, Katherine Yu, Alex G Lee, Marcus R Breese, Stanley G Leung, Hang Xu and 17 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
7.6field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Biological Sample Collection to Advance Research and Treatment: A Fight Osteosarcoma Through European Research and Euro Ewing Consortium Statement.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
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  6. LRRC15-CAR T Cells for the Treatment of Osteosarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 3 institutions in 2 countries.

Courtney R SchottDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0003-2147-6297
Amanda L KoehneDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0002-1397-6964
Leanne C SaylesDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0003-3963-6412
Elizabeth P YoungDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0003-3953-8273
Cuyler LuckDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0002-1150-0057
Katherine YuDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0001-8310-8815
Alex G LeeDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0003-0107-5920
Marcus R BreeseDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0002-6870-0228
Stanley G LeungDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0001-9470-8760
Hang XuDepartments of Genetics and Medicine, Stanford University School of Medicine, Stanford University, Stanford, California.ORCID 0000-0002-5847-655X
Avanthi Tayi ShahDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0002-7125-3406
Heng-Yi LiuDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0009-0007-6715-9867
Aviv SpillingerDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0001-7693-2363
Inge H BehroozfardDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0009-0005-9741-3083
Kieren D MariniDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0001-8399-4757
Phuong T DinhDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0002-0273-1603
María V Pons VenturaDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0009-0003-9516-2052
Emma N VanderboonDepartment of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, Ontario, Canada.ORCID 0009-0006-1503-1768
Florette K HazardDepartment of Pathology, Stanford University School of Medicine, Stanford University, Stanford, California.ORCID 0000-0002-1538-0937
Soo-Jin ChoDepartment of Pathology, University of California San Francisco, San Francisco, California.ORCID 0000-0001-6324-6858
Raffi S AvedianDepartment of Orthopedic Surgery, Stanford University School of Medicine, Stanford University, Stanford, California.ORCID 0000-0001-6224-7410
David G MohlerDepartment of Orthopedic Surgery, Stanford University School of Medicine, Stanford University, Stanford, California.ORCID 0000-0002-8869-139X
Melissa ZimelDepartment of Orthopedic Surgery, University of California San Francisco, San Francisco, California.ORCID 0000-0003-0089-3753
Rosanna WustrackDepartment of Orthopedic Surgery, University of California San Francisco, San Francisco, California.ORCID 0000-0001-8512-5344
Christina CurtisDepartments of Genetics and Medicine, Stanford University School of Medicine, Stanford University, Stanford, California.ORCID 0000-0003-0166-3802
Marina SirotaDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0002-7246-6083
E Alejandro Sweet-CorderoDepartment of Pediatrics, University of California San Francisco, San Francisco, California.ORCID 0000-0002-9787-9351
University of California, San Francisco · USStanford University · USUniversity of Guelph · CA

Funding

Translational InformaticsP30CA082103 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Alan Ashworth · 1999 to 2026
$209.7M
Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI MICHAEL KENNEY · 2007 to 2026
$71.4M
Research Training in Childhood CancerT32CA128583 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Eric Alejandro Sweet-Cordero · 2007 to 2026
$6.0M
Restorative practice in repairing harm and promoting safe and inclusive practices in the laboratory.T32GM136547 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Adrian Erlebacher, Anita Sil · 2020 to 2026
$4.5M
Development of Advanced Preclinical Models for Pediatric Solid TumorsR01CA243555 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SWEET-CORDERO, ERIC ALEJANDRO, VASKE, OLENA MOROZOVA · 2020 to 2024
$3.0M
Utilizing Multi-omics to Facilitate Cancer Biology ResearchR50CA274213 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Alex Lee · 2023 to 2026
$935k
Illumina NovaSeq 6000 Sequencing SystemS10OD028511 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHOW, ERIC D · 2020 to 2020
$583k
PerkinElmer Quantum GX CT-imagerS10OD025022 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI AKHURST, ROSEMARY J · 2019 to 2019
$343k
NCI NIH HHS P30 CA082103NCI NIH HHS P30 CA124435NCI NIH HHS R01 CA243555NCI NIH HHS R50 CA274213NCI NIH HHS T32 CA128583NIGMS NIH HHS T32 GM136547NIH HHS S10 OD025022NIH HHS S10 OD028511
6 · The paper itself

Abstract

purposeModels to study metastatic disease in rare cancers are needed to advance preclinical therapeutics and to gain insight into disease biology. Osteosarcoma is a rare cancer with a complex genomic landscape in which outcomes for patients with metastatic disease are poor. As osteosarcoma genomes are highly heterogeneous, multiple models are needed to fully elucidate key aspects of disease biology and to recapitulate clinically relevant phenotypes. EXPERIMENTAL

designMatched patient samples, patient-derived xenografts (PDX), and PDX-derived cell lines were comprehensively evaluated using whole-genome sequencing and RNA sequencing. The in vivo metastatic phenotype of the PDX-derived cell lines was characterized in both an intravenous and an orthotopic murine model. As a proof-of-concept study, we tested the preclinical effectiveness of a cyclin-dependent kinase inhibitor on the growth of metastatic tumors in an orthotopic amputation model.

resultsPDXs and PDX-derived cell lines largely maintained the expression profiles of the patient from which they were derived despite the emergence of whole-genome duplication in a subset of cell lines. The cell lines were heterogeneous in their metastatic capacity, and heterogeneous tissue tropism was observed in both intravenous and orthotopic models. Single-agent dinaciclib was effective at dramatically reducing the metastatic burden.

conclusionsThe variation in metastasis predilection sites between osteosarcoma PDX-derived cell lines demonstrates their ability to recapitulate the spectrum of the disease observed in patients. We describe here a panel of new osteosarcoma PDX-derived cell lines that we believe will be of wide use to the osteosarcoma research community.

Indexed as

Bone NeoplasmsCyclic N-OxidesIndolizinesOsteosarcomaPyridinium CompoundsAnimalsCell Line, TumorDisease Models, AnimalDrug Evaluation, PreclinicalHumansMiceXenograft Model Antitumor AssaysCyclic N-OxidesdinaciclibIndolizinesPyridinium Compounds

Identifiers

PMID37703185
PMCPMC10870121
OpenAlexW4386708615

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.