Evidence map›Paper›PMID 28088790›Full record

ArticleOncotarget2017

Intraperitoneal immunotherapy with T cells stably and transiently expressing anti-EpCAM CAR in xenograft models of peritoneal carcinomatosis.

Wei Xia Ang, Zhendong Li, Zhixia Chi, Shou-Hui Du, Can Chen, Johan C K Tay, Han Chong Toh, John E Connolly, Xue Hu Xu, Shu Wang

Abstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing 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

72 citing papers in PubMed.

  1. Advances inMolecular therapy. Nucleic acids · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Precision sniper for solid tumors: CAR-NK cell therapy.Cancer immunology, immunotherapy : CII · 2025
    Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Prospects of Synergy: Local Interventions and CAR T Cell Therapy in Solid Tumors.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. RNA-Based Therapeutic Technology.International journal of molecular sciences · 2023
    Review
  19. Review
  20. Review

12 more citing papers are in PubMed but not listed here.

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

10 authors.

Wei Xia AngDepartment of Biological Sciences, National University of Singapore 117543, Singapore.
Zhendong LiDepartment of Biological Sciences, National University of Singapore 117543, Singapore.
Zhixia ChiDepartment of Biological Sciences, National University of Singapore 117543, Singapore.
Shou-Hui DuDepartment of Biological Sciences, National University of Singapore 117543, Singapore.
Can ChenTessa Therapeutics, Pte Ltd., 239351, Singapore.
Johan C K TayDepartment of Biological Sciences, National University of Singapore 117543, Singapore.
Han Chong TohDivision of Medical Oncology, National Cancer Centre, 169610, Singapore.
John E ConnollyProgramme in Translational Immunology, Institute for Molecular and Cell Biology 138648, Singapore.
Xue Hu XuDepartment of Gastrointestinal Surgery, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510150, China.
Shu WangDepartment of Biological Sciences, National University of Singapore 117543, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial cell adhesion molecule (EpCAM) is overexpressed in a wide variety of tumor types, including peritoneal carcinomatosis (PC) from gastrointestinal and gynecological malignancies. To develop a chimeric antigen receptor T (CART) cell therapy approach to treat patients with end-stage PC, we constructed third generation CARs specific to EpCAM using the 4D5MOC-B single chain variable fragment. CART cells were generated with lentiviral transduction and exhibited specific in vitro killing activity against EpCAM-positive human ovarian and colorectal cancer cells. A single intraperitoneal injection of the CART cells eradicated established ovarian xenografts and resulted in significantly prolonged animal survival. Since EpCAM is also expressed on normal epithelium, anti-EpCAM CART cells were generated by mRNA electroporation that display a controlled cytolytic activity with a limited CAR expression duration. Multiple repeated infusions of these RNA CAR-modified T cells delayed disease progression in immunodeficient mice bearing well-established peritoneal ovarian and colorectal xenografts. Thus, our study demonstrates the effectiveness of using anti-EpCAM CAR-expressing T cells for local treatment of PC in mice. The possibility of using this approach for clinical treatment of EpCAM-positive gastrointestinal and gynecological malignancies warrants further validation.

Indexed as

AnimalsCytotoxicity, ImmunologicEpithelial Cell Adhesion MoleculeFemaleHumansImmunotherapy, AdoptiveMicePeritoneal NeoplasmsReceptors, Antigen, T-CellT-LymphocytesXenograft Model Antitumor AssaysEPCAM protein, humanEpithelial Cell Adhesion MoleculeReceptors, Antigen, T-Celladoptive immunotherapychimeric antigen receptorEpCAMperitoneal carcinomatosisT lymphocytes

Identifiers

PMID28088790
PMCPMC5355119

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.