Evidence map›Paper›PMID 40380880›Full record

ReviewHuman vaccines & immunotherapeutics2025

Research hotspots and frontier analysis of the novel immune checkpoint Nectin-4.

Yu Qiao, Wanyu Zhao, Yusen Gou, Yuwei Li, Fang Su, Rui Wang, Jiejun Wang, Haibo Zhang, Lei Sun, Feng Qian and 1 more

Abstract readReview
In one paragraph

Review in Human vaccines & immunotherapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Yu QiaoDepartment of Medical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu Medical University, Bengbu, China.
Wanyu ZhaoDepartment of Biochemistry and Molecular Biology, School of Laboratory Medicine, and Anhui Provincial Key Laboratory of Tumor Evolution and Intelligent Diagnosis and Treatment, Bengbu Medical University, Bengbu, Anhui, China.
Yusen GouShanghai Frontiers Science Center of Drug Target Identification and Delivery, Shanghai Jiao Tong University, Shanghai, China.
Yuwei LiGraduate School, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Fang SuDepartment of Medical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu Medical University, Bengbu, China.
Rui WangDepartment of Medical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu Medical University, Bengbu, China.
Jiejun WangDepartment of Medical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu Medical University, Bengbu, China.
Haibo ZhangDepartment of Medical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu Medical University, Bengbu, China.
Lei SunShanghai Frontiers Science Center of Drug Target Identification and Delivery, Shanghai Jiao Tong University, Shanghai, China.
Feng QianShanghai Frontiers Science Center of Drug Target Identification and Delivery, Shanghai Jiao Tong University, Shanghai, China.
Zishu WangDepartment of Medical Oncology, First Affiliated Hospital of Bengbu Medical University, Bengbu Medical University, Bengbu, China.ORCID 0000-0002-1625-2195

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nectin-4 has emerged as a pivotal therapeutic target for antibody-drug conjugates (ADCs), particularly in advanced urothelial carcinoma (aUC) research. Although extensive literature has been reported on Nectin-4, it is worth noting that no studies have yet systematically investigated the hotspots, cutting-edge directions, and tissue expression of this target using a combination of bibliometric analysis and bioinformatics methods. Findings reveal growing interest in Nectin-4's role in cancer immunotherapy and ADC development. Urothelial carcinoma remains the primary focus, with breast and bladder cancers gaining traction. Key research priorities include optimizing ADC safety profiles, particularly managing cutaneous adverse events. Notably, dual targeting strategies combining Nectin-4 with TROP-2 show promise for next-generation ADC therapies. The study highlights evolving clinical needs, from target validation to treatment optimization, positioning Nectin-4 as a versatile biomarker bridging multiple cancer research domains. These insights emphasize the protein's translational potential while underscoring the importance of balancing therapeutic efficacy with toxicity management in ADC development.

Indexed as

Cell Adhesion MoleculesImmune Checkpoint InhibitorsImmunoconjugatesNectinsAnimalsHumansImmunotherapyUrinary Bladder NeoplasmsCell Adhesion MoleculesImmune Checkpoint InhibitorsImmunoconjugatesNECTIN4 protein, humanNectinsCiteSpaceFrontiersNectin-4research hotspotsVOSviewer

Identifiers

PMID40380880
PMCPMC12087485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.