Evidence map›Paper›PMID 38605247›Full record

ArticleBritish journal of cancer2024

Single-cell sequencing reveals VEGFR as a potential target for CAR-T cell therapy in chordoma.

Huantong Wu, Xinqiang Li, Boyan Zhang, Penghao Liu, Maoyang Qi, Yueqi Du, Can Zhang, Wanru Duan, Zan Chen

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

9 authors at 2 institutions in 2 countries.

Huantong Wu *Department of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Xinqiang Li *Organ Transplantation Center, Affiliated Hospital of Qingdao University, Qingdao, China.
Boyan Zhang *Department of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Penghao LiuDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Maoyang QiDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Yueqi DuDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Can ZhangDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Wanru DuanDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China. duanwanru@xwhosp.org.
Zan ChenDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China. chenzan@ccmu.edu.cn.ORCID 0000-0002-0104-115X
Capital Medical University · CNQingdao University · CN

Funding

Natural Science Foundation of Beijing Municipality (Beijing Natural Science Foundation) No.L212039
6 · The paper itself

Abstract

backgroundChordomas are rare osseous neoplasms with a dismal prognosis when they recur. Here we identified cell surface proteins that could potentially serve as novel immunotherapeutic targets in patients with chordoma.

methodsFourteen chordoma samples from patients attending Xuanwu Hospital Capital Medical University were subjected to single-cell RNA sequencing. Target molecules were identified on chordoma cells and cancer metastasis-related signalling pathways characterised. VEGFR-targeting CAR-T cells and VEGFR CAR-T cells with an additional TGF-β scFv were synthesised and their in vitro antitumor activities were evaluated, including in a primary chordoma organoid model.

resultsSingle-cell transcriptome sequencing identified the chordoma-specific antigen VEGFR and TGF-β as therapeutic targets. VRGFR CAR-T cells and VEGFR/TGF-β scFv CAR-T cells recognised antigen-positive cells and exhibited significant antitumor effects through CAR-T cell activation and cytokine secretion. Furthermore, VEGFR/TGF-β scFv CAR-T cells showed enhanced and sustained cytotoxicity of chordoma cell lines in vitro compared with VRGFR CAR-T cells.

conclusionsThis study provides a comprehensive single-cell landscape of human chordoma and highlights its heterogeneity and the role played by TGF-β in chordoma progression. Our findings substantiate the potential of VEGFR as a target for CAR-T cell therapies in chordoma which, together with modulated TGF-β signalling, may augment the efficacy of CAR-T cells.

Indexed as

ChordomaImmunotherapy, AdoptiveSingle-Cell AnalysisAdultBone NeoplasmsCell Line, TumorFemaleHumansMaleMiddle AgedReceptors, Chimeric AntigenTransforming Growth Factor betaReceptors, Chimeric AntigenTransforming Growth Factor beta

Identifiers

PMID38605247
PMCPMC11091087
OpenAlexW4394724754

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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.