Evidence map›Paper›PMID 42339117›Full record

ReviewFrontiers in oncology2026

The gastrin-releasing peptide receptor in oncology: a comprehensive review of recent advances in targeted radionuclide theranostics.

YunLong Yang, Jiang Fu, ShengJie Tang, Tao Liu, HaiYang Hu, HaiYang Guo, Long Wen, Yang Yang, ChengKuan Liu, GuiYan Yi and 2 more

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

YunLong Yang *Department of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
Jiang Fu *Department of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
ShengJie Tang *Department of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
Tao LiuDepartment of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
HaiYang HuDepartment of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
HaiYang GuoDepartment of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
Long WenDepartment of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
Yang YangDepartment of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
ChengKuan LiuDepartment of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.
GuiYan YiCollege of Medical Technology, Chengdu University of Traditional Chinese Medicine, Chengdu, China.
Li YuDepartment of Physical Examination, Suining Central Hospital, Suining, Sichuan, China.
HaiNing ZhouDepartment of Thoracic Surgery, Suining Central Hospital, Suining, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gastrin-releasing peptide receptor (GRPR) is aberrantly expressed in several malignancies, including prostate cancer, breast cancer, lung cancer, and gastrointestinal stromal tumors, making it an important target for molecular imaging and targeted radionuclide therapy. In recent years, advances in radioligand design, radionuclide selection, and theranostic concepts have substantially promoted the development of GRPR-mediated oncologic applications in nuclear medicine. This review systematically summarizes recent progress in GRPR-targeted radioligands for tumor imaging and radioligand therapy, with particular emphasis on their biological rationale, representative tracers, clinical utility, and major limitations across different tumor types. Overall, GRPR-targeted imaging has demonstrated promising diagnostic value in prostate cancer, estrogen receptor-positive breast cancer, and selected gastrointestinal stromal tumors, and may complement existing imaging modalities. From a therapeutic perspective, the development of high-stability antagonists, metabolic protection strategies, and novel therapeutic radionuclides is driving GRPR-targeted radioligand therapy toward improved therapeutic index and greater translational potential. Nevertheless, several challenges remain, including receptor heterogeneity, physiologic uptake in normal tissues, optimization of pharmacokinetics, the complexity of dual-targeted constructs, and the lack of high-quality prospective clinical evidence. Future progress will likely depend on ligand engineering, dual-target strategies, individualized dosimetry, and the integration of imaging-based treatment assessment into a closed-loop precision theranostic framework.

Indexed as

cancerdiagnosisGRPRradiopharmaceuticaltargeted-therapy

Identifiers

PMID42339117
PMCPMC13283806

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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.