Evidence map›Paper›PMID 36003082›Full record

ArticleFrontiers in molecular biosciences2022

Single-cell transcriptomics uncover the key ferroptosis regulators contribute to cancer progression in head and neck squamous cell carcinoma.

Fei Liu, Lindong Tang, Qing Li, Leihui Chen, Yuyue Pan, Zhao Yin, Jingjun He, Junzhang Tian

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.2field-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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Integrated multi-omics elucidatesFrontiers in immunology · 2025
    Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Iron, Ferroptosis, and Head and Neck Cancer.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Article
  15. Detection of Ferroptosis by Immunohistochemistry and Immunofluorescence.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  16. 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

8 authors at 2 institutions in 1 country.

Fei LiuCancer Screening Center, Department of Health Management, Guangdong Second Provincial General Hospital, Guangdong, China.
Lindong TangInstitute of Hematology School of Medicine Jinan University, Guangdong, China.
Qing LiDepartment of Stomatology Guangdong Second Provincial General Hospital, Guangdong, China.
Leihui ChenDepartment of Stomatology Guangdong Second Provincial General Hospital, Guangdong, China.
Yuyue PanDepartment of Stomatology Guangdong Second Provincial General Hospital, Guangdong, China.
Zhao YinDepartment of Hematology Guangdong Second Provincial General Hospital, Guangdong, China.
Jingjun HeCancer Screening Center, Department of Health Management, Guangdong Second Provincial General Hospital, Guangdong, China.
Junzhang TianCancer Screening Center, Department of Health Management, Guangdong Second Provincial General Hospital, Guangdong, China.
Guangdong Provincial People's Hospital · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mechanism underlying the association between the development of head and neck squamous cell carcinoma (HNSCC) and ferroptosis is unclear. We analyzed the transcriptomes of 5902 single cells from a single-cell RNA-sequencing (scRNA-seq) dataset. They then aggregate into B cells, epithelial cells, fibroblasts, germ cells, mesenchymal cells, cancer stem cells, stem cells, T cells and endometrial cells, respectively. Our study shows that multiple pathways are significantly enriched in HNSCC development including extracellular matrix structural components, humoral immune responses, and muscle contraction. Differentially expressed genes analysis in Pseudotime analysis, pathway and biological function indicated that there was a significant correlation in the ferroptosis pathway. Furthermore, higher ferroptosis potential index (FPI) scores were significantly associated with worse overall survival prognosis in HNSCC patients. Pseudo-temporal, survival analyses and immunohistochemistry identified multiple central genes in HNSCC development, including ACSL1, SLC39A14, TFRC, and PRNP genes, and indicated associated ferroptosis. Overall, our study detected ferroptosis-related features is closely correlated with HNSCC prognosis and development, and deserved candidates suitable for immunotherapy treatment strategies determination for HNSCC patients.

Indexed as

cell heterogeneityferroptosishead and neck squamous cell carcinomaprognosticsingle cell RNA sequencing

Identifiers

PMID36003082
PMCPMC9393303
OpenAlexW4290547238

What OpenQuestion holds

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LicenceCC BY
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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.