Evidence map›Paper›PMID 41774810›Full record

ArticleMolecular pharmaceutics2026

Investigation of Radiolabeled KISS1R Ligands as Promising Tools for Diagnosis and Treatment of Triple-Negative Breast Cancer.

Harun Taş, Martin Schäfer, Aneeba Shuja-Uddin, Ulrike Bauder-Wüst, Luciana Kovacs Dos Santos, Lisa Bartnitzky, Felix Oden, Magdalena Platzk, Tim König, Patrick Leopold Rüther and 6 more

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 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

16 authors.

Harun TaşResearch Group Translational Radiotheranostics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, Heidelberg 69120, Germany.ORCID 0000-0002-1586-5360
Martin SchäferService Unit for Radiopharmaceuticals and Preclinical Studies, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, Heidelberg 69120, Germany.
Aneeba Shuja-UddinResearch Group Translational Radiotheranostics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, Heidelberg 69120, Germany.
Ulrike Bauder-WüstResearch Group Translational Radiotheranostics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, Heidelberg 69120, Germany.
Luciana Kovacs Dos SantosResearch Group Translational Radiotheranostics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, Heidelberg 69120, Germany.
Lisa BartnitzkyBayer AG, Berlin 13342, Germany.
Felix OdenBayer AG, Berlin 13342, Germany.
Magdalena PlatzkBayer AG, Wuppertal 42113, Germany.
Tim KönigBayer AG, Wuppertal 42113, Germany.
Patrick Leopold RütherBayer AG, Wuppertal 42113, Germany.ORCID 0000-0003-4461-9828
Elisabeth PookBayer AG, Wuppertal 42113, Germany.ORCID 0000-0002-6414-3575
Kateřina Dvořáková BendováInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacký University and University Hospital Olomouc, Olomouc 77900, Czech Republic.
Zbyněk NovýInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacký University and University Hospital Olomouc, Olomouc 77900, Czech Republic.
Miloš PetříkInstitute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacký University and University Hospital Olomouc, Olomouc 77900, Czech Republic.ORCID 0000-0003-1334-5916
Urs B HagemannBayer AG, Berlin 13342, Germany.
Martina Benešová-SchäferResearch Group Translational Radiotheranostics, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, Heidelberg 69120, Germany.ORCID 0000-0002-8926-5376

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kisspeptins (KPs) and their receptor (KISS1R) promote metastasis and tumor progression in various cancers such as triple-negative breast cancer (TNBC). Targeting KISS1R holds great promise for molecular imaging and targeted radionuclide therapy of aggressively disseminated cancers. First ligand-based approaches using Ga-68/Lu-177-labeled KPs (KP-10, KP-54) have demonstrated feasibility but suffer from proteolytic degradation and low uptake in KISS1R positive tumors. However, lead structure optimization alone is insufficient, as KISS1R biology remains unexplored in a radiotheranostic context. In this study,

Indexed as

KisspeptinsRadiopharmaceuticalsReceptors, Kisspeptin-1Triple Negative Breast NeoplasmsAnimalsCell Line, TumorCHO CellsCricetulusFemaleHeterocyclic Compounds, 1-RingHumansLigandsLutetiumMolecular ImagingRadioisotopesHeterocyclic Compounds, 1-RingKISS1R protein, humanKisspeptinsLigandsLutetiumRadioisotopesRadiopharmaceuticalsReceptors, Kisspeptin-1GPR54KISS1 receptorkisspeptinradiotheranosticstargeted radionuclide therapy (TRT)triple-negative breast cancer (TNBC)

Identifiers

PMID41774810
PMCPMC13058897

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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.