Evidence map›Paper›PMID 34486479›Full record

ReviewTissue barriers2022

Claudin-18.2 as a therapeutic target in cancers: cumulative findings from basic research and clinical trials.

Daisuke Kyuno, Akira Takasawa, Kumi Takasawa, Yusuke Ono, Tomoyuki Aoyama, Kazufumi Magara, Yuna Nakamori, Ichiro Takemasa, Makoto Osanai

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Tissue barriers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06464965 (A Phase I Clinical Study of Cord Blood-Derived CAR-NK Cells Targeting Claudin18.2 in the Treatment of Advanced Gastric Cancer and Advanced Pancreatic Cancer), which is not on this map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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.

NCT06464965 phase1completednot on this mapstarted 2024, after this paper: background citation

A Phase I Clinical Study of Cord Blood-Derived CAR-NK Cells Targeting Claudin18.2 in the Treatment of Advanced Gastric Cancer and Advanced Pancreatic Cancer

TypeinterventionalSponsorZhejiang Provincial People's HospitalRan2024 to 2025Enrolled9ConditionsGastric Cancer, Pancreas AdenocarcinomaArmsCB CAR-NK18.2, Cyclophosphamide, Fludarabine
3 · Its place in the literature

Who cites it

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
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  8. Review
  9. Advancements in targeted therapy for gastric cancer.Therapeutic advances in gastroenterology · 2026
    Review
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2 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

9 authors at 1 institution in 1 country.

Daisuke KyunoDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.ORCID 0000-0003-4672-535X
Akira TakasawaDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.
Kumi TakasawaDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.
Yusuke OnoDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.
Tomoyuki AoyamaDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.
Kazufumi MagaraDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.
Yuna NakamoriDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.
Ichiro TakemasaDepartment of Surgery, Surgical Oncology and Science, Sapporo Medical University, Sapporo, Japan.
Makoto OsanaiDepartment of Pathology, Sapporo Medical University, Sapporo, Japan.
Sapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Claudins are major components of tight junctions that maintain cell polarity and intercellular adhesion. The dynamics of claudins in cancer cells have attracted attention as a therapeutic target. During carcinogenesis, claudin expression is generally downregulated; however, overexpression of claudin-18.2 has been observed in several types of cancers. Upregulated and mislocalized claudin-18.2 expression in cancer cells has been suggested as a therapeutic target. Research on claudin-18.2 has revealed its involvement in carcinogenesis. Clinical trials using zolbetuximab, a monoclonal antibody targeting claudin-18.2, for patients with advanced cancer yielded positive results with few high-grade adverse events; thus, it is expected to be a novel and effective therapeutic. Here, we review current insights into the role that claudin-18.2 plays in basic cancer research and clinical applications. A better understanding of these roles will facilitate the development of new treatment strategies for cancer patients with poor prognoses.

Indexed as

ClaudinsNeoplasmsCarcinogenesisCell Adhesion MoleculesHumansTight JunctionsCell Adhesion MoleculesClaudinscancerclaudin-18.2Tight junctionzolbetuximab

Identifiers

PMID34486479
PMCPMC8794250
OpenAlexW3198165187

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.