Evidence map›Paper›PMID 37405498›Full record

ArticleMedical oncology (Northwood, London, England)2023

A novel TREM1/DAP12-based multiple chain CAR-T cell targets PTK7 in ovarian cancer therapy.

Tongpeng Xu, Chen Wang, Xiaoyan Wang, Enxiu Wang, Bo Wang, Ming Sun

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. CAR-T Cell Therapy in Ovarian Cancer: Where Are We Now?Diagnostics (Basel, Switzerland) · 2024
    Review
  11. Review
  12. 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

6 authors at 5 institutions in 2 countries.

Tongpeng Xu *Department of Oncology, First Affiliated Hospital, Nanjing Medical University, Nanjing, People's Republic of China.
Chen Wang *Nanjing CART Medical Technology Co., Ltd, Nanjing, 210032, People's Republic of China.
Xiaoyan Wang *Reproductive Center, Qingdao Women and Children's Hospital, Qingdao Women and Children's Hospital Affiliated to Qingdao University, Qingdao, 266034, China.
Enxiu WangNanjing CART Medical Technology Co., Ltd, Nanjing, 210032, People's Republic of China. wangenxiu@cart-med.com.
Bo WangDepartment of Medical Oncology, The Seventh Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518107, People's Republic of China. wangb68377@sina.com.
Ming SunSuzhou Cancer Center Core Laboratory, Nanjing Medical University Affiliated Suzhou Hospital, Suzhou Municipal Hospital, Gusu School, Baita West Road #16, Suzhou, 215001, People's Republic of China. sunming348@hotmail.com.ORCID http://orcid.org/0000-0002-1173-2288
Affiliated Hospital of Youjiang Medical University for Nationalities · CNNanjing Medical University · CNQingdao University · CNSun Yat-sen University · CNSuzhou Municipal Hospital · CN

Funding

National Natural Science Foundation of China 81970177National Natural Science Foundation of China 82060559
6 · The paper itself

Abstract

While CAR-T cell therapy has shown success against hematological tumors, its effectiveness for solid tumors, including ovarian cancer, remains unsatisfactory. This study aimed to develop and evaluate the efficacy of novel chimeric antigen receptor T (CAR-T) cells targeting PTK7 through TREM1/DAP12 signaling against ovarian cancer. The expression of PTK7 in ovarian cancer tissues and cells was evaluated using immunohistochemical staining and flow cytometric analysis. The anti-tumor effects of PTK7 CAR-T cells were assessed in vitro using real-time cell analysis and enzyme-linked immunosorbent assay, and in vivo using a xenograft tumor model. PTK7 was significantly expressed in ovarian cancer tissues and cells. PTK7-targeting CAR-T cells based on TREM1/DAP12 signaling exhibited potent cytotoxicity against ovarian cancer cells expressing PTK7 in vitro, and effectively eradicated tumors in vivo. Our findings suggest that TREM1/DAP12-based PTK7 CAR-T cells have potential as a treatment strategy for ovarian cancer. Further studies are needed to evaluate the safety and efficacy of this approach in clinical trials.

Indexed as

Ovarian NeoplasmsReceptors, Chimeric AntigenCell Adhesion MoleculesCell Line, TumorFemaleHumansImmunotherapy, AdoptiveReceptor Protein-Tyrosine KinasesT-LymphocytesTriggering Receptor Expressed on Myeloid Cells-1Xenograft Model Antitumor AssaysCell Adhesion MoleculesPTK7 protein, humanReceptor Protein-Tyrosine KinasesReceptors, Chimeric AntigenTREM1 protein, humanTriggering Receptor Expressed on Myeloid Cells-1CAR-T cellDAP12Ovarian cancerPTK7TREM1

Identifiers

PMID37405498
OpenAlexW4383186900

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.