Evidence map›Paper›PMID 42554513›Full record

ArticleMolecular pharmaceutics2026

Macropa-Based 225Ac-Labeled RGD Peptides for Targeted Alpha Therapy.

Hiroaki Echigo, Masayuki Munekane, Takeshi Fuchigami, Kenji Mishiro, Hidetoshi Kikunaga, Kazuaki Tsukada, Takuya Yokokita, Kenji Shirasaki, Jun Ichinose, Eiichi Hinoi and 2 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

12 authors.

Hiroaki EchigoGraduate School of Medical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa920-1192, Japan.
Masayuki MunekaneGraduate School of Medical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa920-1192, Japan.
Takeshi FuchigamiGraduate School of Medical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa920-1192, Japan.ORCID 0000-0001-8141-1212
Kenji MishiroGraduate School of Medical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa920-1192, Japan.ORCID 0000-0002-5071-7574
Hidetoshi KikunagaResearch Center for Accelerator and Radioisotope Science (RARiS), Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi982-0826, Japan.
Kazuaki TsukadaResearch Center for Accelerator and Radioisotope Science (RARiS), Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi982-0826, Japan.
Takuya YokokitaResearch Center for Accelerator and Radioisotope Science (RARiS), Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi982-0826, Japan.
Kenji ShirasakiInstitute for Radiation Sciences (IRS), The University of Osaka, 1-1 Machikaneyama-cho, Toyonaka, Osaka560-0043, Japan.
Jun IchinoseDepartment of Advanced Nuclear Medicine Sciences, National Institutes for Quantum Science and Technology (QST), 4-9-1 Anagawa, Inage-ku, Chiba263-8555, Japan.
Eiichi HinoiDepartment of Bioactive Molecules, Pharmacology, Gifu Pharmaceutical University, Gifu501-1196, Japan.
Seigo KinuyaDepartment of Nuclear Medicine, Kanazawa University Hospital, Kanazawa University, Takara-machi 13-1, Kanazawa, Ishikawa920-8641, Japan.
Kazuma OgawaGraduate School of Medical Sciences, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa920-1192, Japan.ORCID 0000-0002-1691-7302

Funding

Japan Society for the Promotion of Science 24K02394Japan Society for the Promotion of Science 24KJ1195Japan Society for the Promotion of Science 25K22607Terumo Foundation for Life Sciences and Arts NA
6 · The paper itself

Abstract

Macropa has formed more stable complexes with 225Ac, although DOTA has been extensively used as a chelator for 225Ac. This study aimed to design and synthesize two novel 225Ac-labeled RGD peptides, [225Ac]Ac-Macropa-c(RGDyK) ([225Ac]1) and [225Ac]Ac-Macropa-[c(RGDyK)]2 ([225Ac]2), and to evaluate their potential for targeted alpha therapy (TAT) of glioblastoma. Further, whether combination therapy with homoarginine (hArg), a modulator of lysosomal function, could further improve therapeutic efficacy was investigated. In Colon-26 cells, [225Ac]2 demonstrated significantly higher cellular uptake and cytotoxicity than [225Ac]1. In Colon-26 tumor-bearing mice, [225Ac]2 exhibited higher tumor accumulation and significant tumor growth inhibition. In GL261 glioblastoma cells, [225Ac]2 showed comparable cellular uptake to that in Colon-26 cells, and combination with hArg in vitro improved its cytotoxicity. However, no significant difference in therapeutic efficacy was observed between the hArg-treated and control groups in the orthotopic GL261 glioblastoma mouse model. The results of this study indicate the potential of 225Ac-labeled RGD peptides incorporating Macropa as a chelator as promising agents for TAT. However, the further optimization of combination strategies and pharmacokinetics is required.

Indexed as

ActiniumAlpha ParticlesGlioblastomaOligopeptidesAnimalsCell Line, TumorFemaleHumansMiceTissue DistributionActiniumActinium-225arginyl-glycyl-aspartic acidOligopeptidesactinium-225 (225Ac)glioblastomamacropaRGD peptidetargeted alpha therapy (TAT)

Identifiers

PMID42554513
PMCPMC13556129

What Socratic holds

Textmetadata
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 Socratic graph.