Evidence map›Paper›PMID 39537365›Full record

ReviewMolecular pharmaceutics2024

Trop2-Targeted Molecular Imaging in Solid Tumors: Current Advances and Future Outlook.

Yongshun Liu, Wenpeng Huang, Rachel J Saladin, Jessica C Hsu, Weibo Cai, Lei Kang

Abstract readReview
In one paragraph

Review in Molecular pharmaceutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Coordinated Expression of ADC TargetsCurrent issues in molecular biology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Visualization of the Spiral Ganglion Neuron in Vivo Using a NovelAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  10. Review
  11. [American journal of nuclear medicine and molecular imaging · 2025
    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

6 authors.

Yongshun LiuDepartment of Nuclear Medicine, Peking University First Hospital, Beijing 100034, China.
Wenpeng HuangDepartment of Nuclear Medicine, Peking University First Hospital, Beijing 100034, China.
Rachel J SaladinDepartments of Radiology and Medical Physics, University of Wisconsin─Madison, Madison, Wisconsin 53705, United States.
Jessica C HsuDepartments of Radiology and Medical Physics, University of Wisconsin─Madison, Madison, Wisconsin 53705, United States.
Weibo CaiDepartments of Radiology and Medical Physics, University of Wisconsin─Madison, Madison, Wisconsin 53705, United States.ORCID 0000-0003-4641-0833
Lei KangDepartment of Nuclear Medicine, Peking University First Hospital, Beijing 100034, China.ORCID 0000-0001-8729-4547

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
NCI NIH HHS P30 CA014520
6 · The paper itself

Abstract

Trophoblast cell surface antigen 2 (Trop2), a transmembrane glycoprotein, plays a dual role in physiological and pathological processes. In healthy tissues, Trop2 facilitates development and orchestrates intracellular calcium signaling. However, its overexpression in numerous solid tumors shifts its function toward driving cell proliferation and metastasis, thus leading to a poor prognosis. The clinical relevance of Trop2 is underscored by its utility as both a biomarker for diagnostic imaging and a target for therapy. Notably, the U.S. Food and Drug Administration (FDA) has approved sacituzumab govitecan (SG), a novel Trop2-targeted agent, for treating triple-negative breast cancer (TNBC) and refractory urothelial cancer, highlighting the significance of Trop2 in clinical oncology. Molecular imaging, a powerful tool for visualizing and quantifying biological phenomena at the molecular and cellular levels, has emerged as a critical technique for studying Trop2. This approach encompasses various modalities, including optical imaging, positron emission tomography (PET), single photon emission computed tomography (SPECT), and targeted antibodies labeled with radioactive isotopes. Incorporating Trop2-targeted molecular imaging into clinical practice is vital for the early detection, prognostic assessment, and treatment planning of a broad spectrum of solid tumors. Our review captures the latest progress in Trop2-targeted molecular imaging, focusing on both diagnostic and therapeutic applications across diverse tumor types, including lung, breast, gastric, pancreatic, prostate, and cervical cancers, as well as salivary gland carcinomas. We critically evaluate the current state by examining the relevant applications, diagnostic accuracy, therapeutic efficacy, and inherent limitations. Finally, we analyze the challenges impeding widespread clinical application and offer insights into strategies for advancing the field, thereby guiding future research endeavors.

Indexed as

Antigens, NeoplasmCell Adhesion MoleculesMolecular ImagingNeoplasmsAnimalsAntibodies, Monoclonal, HumanizedBiomarkers, TumorCamptothecinHumansImmunoconjugatesPositron-Emission TomographyTriple Negative Breast NeoplasmsAntibodies, Monoclonal, HumanizedAntigens, NeoplasmBiomarkers, TumorCamptothecinCell Adhesion MoleculesImmunoconjugatessacituzumab govitecanTACSTD2 protein, humanDiagnosticMolecular imagingSolid tumorTherapeuticTrophoblast cell surface antigen 2

Identifiers

PMID39537365
PMCPMC11832138

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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.