Evidence map›Paper›PMID 37868989›Full record

ArticleFrontiers in immunology2023

A humanized orthotopic mouse model for preclinical evaluation of immunotherapy in Ewing sarcoma.

Wen Luo, Hai Hoang, Yanling Liao, Jian Pan, Janet Ayello, Mitchell S Cairo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. 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

6 authors at 1 institution in 1 country.

Wen LuoDepartment of Pediatrics, New York Medical College, Valhalla, NY, United States.
Hai HoangDepartment of Pediatrics, New York Medical College, Valhalla, NY, United States.
Yanling LiaoDepartment of Pediatrics, New York Medical College, Valhalla, NY, United States.
Jian PanDepartment of Pediatrics, New York Medical College, Valhalla, NY, United States.
Janet AyelloDepartment of Pediatrics, New York Medical College, Valhalla, NY, United States.
Mitchell S CairoDepartment of Pediatrics, New York Medical College, Valhalla, NY, United States.
New York Medical College · US

Funding

Project 4:Targeting M2-like Macrophages and MDSC with Myelolytic-VirotherapyU54CA232561 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI CRIPE, TIMOTHY P · 2019 to 2023
$12.1M
NCI NIH HHS U54 CA232561
6 · The paper itself

Abstract

The advent of novel cancer immunotherapy approaches is revolutionizing the treatment for cancer. Current small animal models for most cancers are syngeneic or genetically engineered mouse models or xenograft models based on immunodeficient mouse strains. These models have been limited in evaluating immunotherapy regimens due to the lack of functional human immune system. Development of animal models for bone cancer faces another challenge in the accessibility of tumor engraftment sites. Here, we describe a protocol to develop an orthotopic humanized mouse model for a bone and soft tissue sarcoma, Ewing sarcoma, by transplanting fresh human cord blood CD34

Indexed as

Bone NeoplasmsOsteosarcomaSarcoma, EwingAnimalsCD47 AntigenDisease Models, AnimalHumansImmunotherapyMiceT-LymphocytesCD47 Antigenbone sarcomacord bloodhumanized mouse modelimmunotherapyorthotopic modelpediatric cancer

Identifiers

PMID37868989
PMCPMC10587429
OpenAlexW4387403679

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.