Evidence map›Paper›PMID 33539630›Full record

ArticleCancer science2021

Anti-tumor efficacy of human anti-c-met CAR-T cells against papillary renal cell carcinoma in an orthotopic model.

Jun-Ich Mori, Keishi Adachi, Yukimi Sakoda, Takahiro Sasaki, Shunsuke Goto, Hiroaki Matsumoto, Yoji Nagashima, Hideyasu Matsuyama, Koji Tamada

Abstract read
In one paragraph

Article in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
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  5. Review
  6. Article
  7. Review
  8. MET Oncogene Targeting for Cancer Immunotherapy.International journal of molecular sciences · 2024
    Review
  9. Review
  10. Article
  11. CAR-T Cell Therapy: Advances in Kidney-Related Diseases.Kidney diseases (Basel, Switzerland) · 2024
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
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  19. Article
  20. 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

9 authors.

Jun-Ich MoriDepartment of Immunology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Keishi AdachiDepartment of Immunology, Yamaguchi University Graduate School of Medicine, Ube, Japan.ORCID https://orcid.org/0000-0002-7524-2886
Yukimi SakodaDepartment of Immunology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Takahiro SasakiDepartment of Immunology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Shunsuke GotoDepartment of Immunology, Yamaguchi University Graduate School of Medicine, Ube, Japan.
Hiroaki MatsumotoDepartment of Urology, Yamaguchi University Graduate School of Medicine, Ube, Japan.ORCID https://orcid.org/0000-0003-0568-1258
Yoji NagashimaDepartment of Surgical Pathology, Tokyo Women's Medical University, Tokyo, Japan.
Hideyasu MatsuyamaDepartment of Urology, Yamaguchi University Graduate School of Medicine, Ube, Japan.ORCID https://orcid.org/0000-0001-5607-7769
Koji TamadaDepartment of Immunology, Yamaguchi University Graduate School of Medicine, Ube, Japan.ORCID https://orcid.org/0000-0002-3098-2565

Funding

Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research (C) / 18K07268
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR)-T cell therapy has shown salient efficacy in cancer immunotherapy, particularly in the treatment of B cell malignancies. However, the efficacy of CAR-T for solid tumors remains inadequate. In this study, we displayed that c-met is an appropriate therapeutic target for papillary renal cell carcinoma (PRCC) using clinical samples, developed an anti-human c-met CAR-T cells, and investigated the anti-tumor efficacy of the CAR-T cells using an orthotopic mouse model as pre-clinical research. Administration of the anti-c-met CAR-T cells induced marked infiltration of the CAR-T cells into the tumor tissue and unambiguous suppression of tumor growth. Furthermore, in combination with axitinib, the anti-tumor efficacy of the CAR-T cells was synergistically augmented. Taken together, our current study demonstrated the potential for clinical application of anti-c-met CAR-T cells in the treatment of patients with PRCC.

Indexed as

AgedAnimalsAntibodiesAntigens, NeoplasmCarcinoma, Renal CellCell Line, TumorCells, CulturedDisease Models, AnimalFemaleHumansImmunotherapyKidney NeoplasmsMaleMiceMice, Inbred NODProto-Oncogene Proteins c-metAntibodiesAntigens, NeoplasmMET protein, humanProto-Oncogene Proteins c-metReceptors, Chimeric AntigenaxitinibCAR-T cellsc-metorthotopic modelpapillary renal cell carcinoma

Identifiers

PMID33539630
PMCPMC8019206

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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.