Evidence map›Paper›PMID 37545523›Full record

ArticleFrontiers in immunology2023

Modeling the tumor microenvironment of anaplastic thyroid cancer: an orthotopic tumor model in C57BL/6 mice.

Zhen Xu, Hyo Shik Shin, Yoo Hyung Kim, Seong Yun Ha, Jae-Kyung Won, Su-Jin Kim, Young Joo Park, Sareh Parangi, Sun Wook Cho, Kyu Eun Lee

Abstract 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. B7-H3 and CSPG4-targeted CAR T cells as potent effectors in anaplastic thyroid cancer.Journal of experimental & clinical cancer research : CR · 2025
    Article
  2. Review
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.

Zhen XuCancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Hyo Shik ShinDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Yoo Hyung KimDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Seong Yun HaCancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jae-Kyung WonDepartment of Pathology, Seoul National University Hospital, Seoul, Republic of Korea.
Su-Jin KimCancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.
Young Joo ParkDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Sareh ParangiDepartment of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.
Sun Wook ChoDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Kyu Eun LeeCancer Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Securing a well-established mouse model is important in identifying and validating new therapeutic targets for immuno-oncology. The C57BL/6 mouse is one of the most fully characterised immune system of any animal and provides powerful platform for immuno-oncology discovery. An orthotopic tumor model has been established using TBP3743 (murine anaplastic thyroid cancer [ATC]) cells in B6129SF1 hybrid mice, this model has limited data on tumor immunology than C57BL/6 inbred mice. This study aimed to establish a novel orthotopic ATC model in C57BL/6 mice and characterize the tumor microenvironment focusing immunity in the model. Methods: Adapted TBP3743 cells were generated via Results: The adapted TBP3743 cells de-differentiated but exhibited cell morphology, viability, and migration/invasion potential comparable with those of original cells Conclusion: A novel orthotopic tumor model of ATC was established in C57BL/6 mice. Compared with the original B6129SF1 murine model, the novel model exhibited more aggressive tumor cell behaviours and strong immune responses. We expect that this novel model contributes to the understanding tumor microenvironment and provides the platform for drug development.

Indexed as

Thyroid Carcinoma, AnaplasticThyroid NeoplasmsAnimalsHumansKi-67 AntigenMiceMice, Inbred C57BLTumor MicroenvironmentKi-67 Antigenanaplastic thyroid cancerBRAF V600Eimmunotherapysyngeneictumor microenvironment

Identifiers

PMID37545523
PMCPMC10403231

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Registered trials

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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.