Evidence map›Paper›PMID 38816233›Full record

ArticleJournal for immunotherapy of cancer2024

Interactions between LAMP3+ dendritic cells and T-cell subpopulations promote immune evasion in papillary thyroid carcinoma.

Zhiyuan Wang, Xiaoyu Ji, Ye Zhang, Fan Yang, Hongyue Su, Hao Zhang, Zhendong Li, Wenqian Zhang, Wei Sun

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

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  4. Cancers · 2026
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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.

Zhiyuan Wang *Department of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.
Xiaoyu Ji *Department of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.
Ye Zhang *The First Laboratory of Cancer Institute, The First Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.
Fan YangDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.
Hongyue SuDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.
Hao ZhangDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.
Zhendong LiDepartment of Head and Neck Surgery, Cancer Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.
Wenqian ZhangDepartment of Head and Neck Surgery, Cancer Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China 652603034@qq.com Sun19890208@126.com.
Wei SunDepartment of Thyroid Surgery, The First Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China 652603034@qq.com Sun19890208@126.com.ORCID http://orcid.org/0000-0003-1952-128X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of papillary thyroid cancer (PTC) continues to rise all over the world, 10-15% of the patients have a poor prognosis. Although immunotherapy has been applied in clinical practice, its therapeutic efficacy remains far from satisfactory, necessitating further investigation of the mechanism of PTC immune remodeling and exploration of novel treatment targets.

methodsThis study conducted a single-cell RNA sequencing (scRNA-seq) analysis using 18 surgical tissue specimens procured from 14 patients diagnosed with adjacent tissues, non-progressive PTC or progressive PTC. Key findings were authenticated through spatial transcriptomics RNA sequencing, immunohistochemistry, multiplex immunohistochemistry, and an independent bulk RNA-seq data set containing 502 samples.

resultsA total of 151,238 individual cells derived from 18 adjacent tissues, non-progressive PTC and progressive PTC specimens underwent scRNA-seq analysis. We found that progressive PTC exhibits the following characteristics: a significant decrease in overall immune cells, enhanced immune evasion of tumor cells, and disrupted antigen presentation function. Moreover, we identified a subpopulation of lysosomal associated membrane protein 3 (LAMP3

conclusionOur findings expound valuable insights into the role of the interaction between LAMP3

Indexed as

Dendritic CellsThyroid Cancer, PapillaryFemaleHumansLysosomal-Associated Membrane Protein 3MaleMiddle AgedNeoplasm ProteinsThyroid NeoplasmsT-Lymphocyte SubsetsTumor EscapeTumor MicroenvironmentLAMP3 protein, humanLysosomal-Associated Membrane Protein 3Neoplasm ProteinsDendriticEscape/evasionHead and Neck CancerImmunosuppressionT cell

Identifiers

PMID38816233
PMCPMC11141193

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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.