Evidence map›Paper›PMID 38390321›Full record

ArticleFrontiers in immunology2024

Efficacy of MUC1-targeted CAR-NK cells against human tongue squamous cell carcinoma.

Xiaolan Lin, Tian Guan, Yun Li, Yanchun Lin, Guowei Huang, Yan Lin, Pingnan Sun, Congzhu Li, Jiang Gu, Haoyu Zeng and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
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  6. The Application of iPSCs in Tumour Immunotherapy.Expert reviews in molecular medicine · 2025
    Review
  7. Precision sniper for solid tumors: CAR-NK cell therapy.Cancer immunology, immunotherapy : CII · 2025
    Review
  8. Rendering NK Cells Antigen-Specific for the Therapy of Solid Tumours.International journal of molecular sciences · 2025
    Review
  9. Review
  10. Review
  11. Review
  12. MUC16: clinical targets with great potential.Clinical and experimental medicine · 2024
    Review
  13. 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

11 authors at 2 institutions in 1 country.

Xiaolan Lin *Department of Radiation Oncology, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, China.
Tian Guan *Guangdong Procapzoom Bioscience Inc., Guangzhou, China.
Yun LiGuangdong Procapzoom Bioscience Inc., Guangzhou, China.
Yanchun LinGuangdong Procapzoom Bioscience Inc., Guangzhou, China.
Guowei HuangGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Shantou University Medical College, Shantou, Guangdong, China.
Yan LinDepartment of Medical Imaging, the Second Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
Pingnan SunDepartment of Stem Cell Research Center, Shantou University Medical College, Shantou, Guangdong, China.
Congzhu LiDepartment of Gynecological Oncology, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, China.
Jiang GuGuangdong Provincial Key Laboratory of Infectious Diseases and Molecular Immunopathology, Shantou University Medical College, Shantou, Guangdong, China.
Haoyu ZengGuangdong Procapzoom Bioscience Inc., Guangzhou, China.
Changchun MaDepartment of Radiation Oncology, Cancer Hospital of Shantou University Medical College, Shantou, Guangdong, China.
Shantou University · CNGuangdong Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The clinical efficacy of CAR-NK cells against CD19-expressing blood cancers has been demonstrated, and they have shown potential for treating solid tumors as well. However, the efficacy of CAR-NK cells for treating human oral tongue squamous cell carcinoma (OTSCC) has not been examined. Methods: We assessed MUC1 expression in human OTSCC tissue and a cell line using immunohistochemistry and immunofluorescence. We constructed NK cells that express CAR targeted to MUC1 from pluripotent stem cells (iPSC-derived MUC1-targeted CAR-NK cells) and evaluated their effectiveness against OTSCC Results: MUC1 expression was detected in 79.5% (66/83) of all OTSCC patients and 72.7% (24/33) of stage III and IV. In stage III and IV MUC1 positive OTSCC, 63.6% (21/33) and 48.5% (16/33) patients had a MUC1-positive cancer cell rate of more than 50% and 80%, respectively. The iPSC-derived MUC1-targeted CAR-NK cells exhibited significant cytotoxicity against MUC1-expressing OTSCC cells Conclusion: The MUC1-targeted CAR-NK cells had significant efficacy against human OTSCC, and their promising therapeutic response warrants further clinical trials.

Indexed as

Carcinoma, Squamous CellTongue NeoplasmsAnimalsCell LineHumansKiller Cells, NaturalMiceMucin-1TongueMUC1 protein, humanMucin-1chimeric antigen receptor (CAR)induced pluripotent stem (iPS) celliPSC-derived MUC1-targeted CAR-NK cellsmucin 1NK cells therapyoral tongue squamous cell carcinoma

Identifiers

PMID38390321
PMCPMC10882221
OpenAlexW4391671173

What OpenQuestion holds

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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.