Evidence map›Paper›PMID 42010078›Full record

ArticleDoklady. Biochemistry and biophysics2026

Modular Nanotransporters Containing Anti-PSMA Nanobodies Are Able to Penetrate into the Nuclei of Prostate Cancer Cells.

Y V Khramtsov, A V Ulasov, T A Slastnikova, T N Lupanova, A A Rosenkranz, G P Georgiev, A S Sobolev

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Article in Doklady. Biochemistry and biophysics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Y V KhramtsovInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
A V UlasovInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
T A SlastnikovaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
T N LupanovaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
A A RosenkranzInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
G P GeorgievInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
A S SobolevInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia. alsobolev@yandex.ru.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polypeptide modular nanotransporters (MNTs) were engineered as a targeted delivery platform for prostate cancer cells. The constructs integrate a ligand module to facilitate specific cellular binding and internalization, and a nuclear localization signal (NLS) to enable subsequent nuclear translocation. Two distinct ligand modules were utilized: (a) a nanobody targeting prostate-specific membrane antigen (anti-PSMA) and (b) a gastrin-releasing peptide (GRP) fragment targeting the GRP receptor (GRPR). It was shown that all modules within MNT-antiPSMA and MNT-GRP retained their functional properties. The MNT-antiPSMA construct demonstrated the capacity to accumulate specifically in the nuclei of prostate cancer cells with both low and high PSMA expression. Conversely, MNT-GRP exhibited selective nuclear entry exclusively in cells characterized by high GRPR expression.

Indexed as

Antigens, SurfaceCell NucleusGlutamate Carboxypeptidase IIProstatic NeoplasmsSingle-Domain AntibodiesCell Line, TumorGastrin-Releasing PeptideHumansMaleAntigens, SurfaceFOLH1 protein, humanGastrin-Releasing PeptideGlutamate Carboxypeptidase IISingle-Domain Antibodiesantibody-like moleculesdiphtheria toxin translocation domainintracellular transportmodular nanotransportersprostate cancerprostate-specific membrane antigentargeted drug delivery

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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.