Evidence map›Paper›PMID 37990009›Full record

ArticleNature communications2023

Genomic profiling of subcutaneous patient-derived xenografts reveals immune constraints on tumor evolution in childhood solid cancer.

Funan He, Abhik M Bandyopadhyay, Laura J Klesse, Anna Rogojina, Sang H Chun, Erin Butler, Taylor Hartshorne, Trevor Holland, Dawn Garcia, Korri Weldon and 18 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. 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
2.9field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Preclinical Activity of the B7-H3-Targeting Antibody-Drug Conjugate Vobramitamab Duocarmazine in Pediatric Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. GDF-15 Predicts Epithelioid Hemangioendothelioma Aggressiveness and Is Downregulated by Sirolimus through ATF4/ATF5 Suppression.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  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

28 authors at 3 institutions in 1 country.

Funan He *Greehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.ORCID 0000-0002-4592-4034
Abhik M Bandyopadhyay *Greehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Laura J KlesseDepartment of Pediatrics, Division of Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0003-1323-7720
Anna RogojinaGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Sang H ChunDepartment of Biochemistry and Structural Biology, University of Texas Health Science Center, San Antonio, TX, USA.
Erin ButlerDepartment of Pediatrics, Division of Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Taylor HartshorneDepartment of Pediatrics, Division of Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0009-0009-2036-9757
Trevor HollandGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Dawn GarciaGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Korri WeldonGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Luz-Nereida Perez PradoGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Anne-Marie LangevinDepartment of Pediatrics, University of Texas Health Science Center, San Antonio, TX, USA.
Allison C GrimesGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Aaron SugalskiDepartment of Pediatrics, University of Texas Health Science Center, San Antonio, TX, USA.
Shafqat ShahDepartment of Pediatrics, University of Texas Health Science Center, San Antonio, TX, USA.
Chatchawin AssanasenDepartment of Pediatrics, University of Texas Health Science Center, San Antonio, TX, USA.
Zhao LaiGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Yi ZouGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Dias KurmashevGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Lin XuDepartment of Pediatrics, Division of Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0001-5815-4457
Yang XieHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Yidong ChenGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Xiaojing WangGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.ORCID 0000-0002-2631-4708
Gail E TomlinsonGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Stephen X SkapekDepartment of Pediatrics, Division of Hematology/Oncology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Peter J HoughtonGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA.
Raushan T KurmashevaGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA. kurmasheva@uthscsa.edu.ORCID 0000-0003-3212-2363
Siyuan ZhengGreehey Children's Cancer Research Institute, University of Texas Health Science Center, San Antonio, TX, USA. zhengs3@uthscsa.edu.ORCID 0000-0002-1031-9424
The University of Texas Health Science Center at San Antonio · USChildren's Medical Center · USThe University of Texas Southwestern Medical Center · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
A Testing Program to Identify Novel Agents for Treatment of Pediatric and AYA High-Risk Sarcoma, Kidney and Liver CancerU01CA263981 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Raushan Kurmasheva · 2021 to 2026
$3.2M
Advancing Cancer Research Through Next Generation Sequencing at Mays Cancer Center of UT Health San AntonioR50CA265339 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Zhao Lai · 2022 to 2026
$957k
High Throughput DNA Sequencer: Illumina HiSeq 3000 SequencerS10OD021805 · OD · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LAI, ZHAO · 2016 to 2016
$600k
Illumina NovaSeq 6000 Sequencing SystemS10OD030311 · OD · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LAI, ZHAO · 2021 to 2021
$600k
NCI NIH HHS P30 CA054174NCI NIH HHS R50 CA265339NCI NIH HHS U01 CA263981NIH HHS S10 OD021805NIH HHS S10 OD030311
6 · The paper itself

Abstract

Subcutaneous patient-derived xenografts (PDXs) are an important tool for childhood cancer research. Here, we describe a resource of 68 early passage PDXs established from 65 pediatric solid tumor patients. Through genomic profiling of paired PDXs and patient tumors (PTs), we observe low mutational similarity in about 30% of the PT/PDX pairs. Clonal analysis in these pairs show an aggressive PT minor subclone seeds the major clone in the PDX. We show evidence that this subclone is more immunogenic and is likely suppressed by immune responses in the PT. These results suggest interplay between intratumoral heterogeneity and antitumor immunity may underlie the genetic disparity between PTs and PDXs. We further show that PDXs generally recapitulate PTs in copy number and transcriptomic profiles. Finally, we report a gene fusion LRPAP1-PDGFRA. In summary, we report a childhood cancer PDX resource and our study highlights the role of immune constraints on tumor evolution.

Indexed as

NeoplasmsAnimalsChildDisease Models, AnimalGenomicsHeterograftsHumansMutationTranscriptomeXenograft Model Antitumor Assays

Identifiers

PMID37990009
PMCPMC10663468
OpenAlexW4388900980

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.