Evidence map›Paper›PMID 35084549›Full record

ArticleCancer immunology, immunotherapy : CII2022

Single-cell transcriptome profiling reveals intra-tumoral heterogeneity in human chordomas.

Wanru Duan, Boyan Zhang, Xinqiang Li, Wei Chen, Shanhang Jia, Zong Xin, Qiang Jian, Fengzeng Jian, Dean Chou, Zan Chen

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 37 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

10 authors at 4 institutions in 3 countries.

Wanru DuanDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Boyan ZhangDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Xinqiang LiDepartment of Liver Transplantation, The Affiliated Hospital of Qingdao University, Qingdao, China.
Wei ChenBeijing Advanced Innovation Center for Biomedical Engineering, School of Engineering Medicine, Beihang University, Beijing, China.
Shanhang JiaDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Zong XinDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Qiang JianDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Fengzeng JianDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
Dean ChouDepartment of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Zan ChenDepartment of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China. chenzan66@163.com.ORCID http://orcid.org/0000-0002-0104-115X
Capital Medical University · CNBeijing Advanced Sciences and Innovation Center · CNQingdao University · CNUniversity of California, San Francisco · US

Funding

Chinese Academy of Medical Sciences #201920200501
6 · The paper itself

Abstract

Chordoma is a rare and aggressive bone tumor. An accurate investigation of tumor heterogeneity is necessary for the development of effective therapeutic strategies. This study aims to assess the poorly understood tumor heterogeneity of chordomas and identify potential therapeutic targets. Single-cell RNA sequencing was performed to delineate the transcriptomic landscape of chordomas. Six tumor samples of chordomas were obtained, and 33,737 cells passed the quality control test and were analyzed. The main cellular populations identified with specific markers were as follows: chordoma cells (16,052 [47.6%]), fibroblasts (6945 [20.6%]), mononuclear phagocytes (4734 [14.0%]), and T/natural killer (NK) cells (3944 [11.7%]). Downstream analysis of each cell type was performed. Six subclusters of chordomas exhibited properties of an epithelial-like extracellular matrix, stem cells, and immunosuppressive activity. Although few immune checkpoints were detected on cytotoxic immune cells such as T and NK cells, a strong immunosuppressive effect was exerted on the Tregs and M2 macrophages. In addition, the cellular interactions were indicative of enhancement of the TGF-β signaling pathway being the main mechanism for tumor progression, invasion, and immunosuppression. These findings, especially from the analysis of molecular targeted therapy and tumor immune microenvironment, may help in the identification of therapeutic targets in chordomas.

Indexed as

Bone NeoplasmsChordomaGene Expression ProfilingHumansTranscriptomeTumor MicroenvironmentChordomasCytotoxic immune cellsImmunosuppressive activitySingle-cell RNA sequencing

Identifiers

PMID35084549
PMCPMC10992276
OpenAlexW4220927656

What OpenQuestion holds

Textmetadata
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.