Synthesis and Preclinical Evaluation of Urea-Based Prostate-Specific Membrane Antigen-Targeted Conjugates Labeled with 177Lu; ACS Pharmacology & Translational Science; Vol. 7, iss. 5

Dettagli Bibliografici
Parent link:ACS Pharmacology & Translational Science.— .— Washington: ACS Publications
Vol. 7, iss. 5.— 2024.— P. 1457–1473
Altri autori: Machulkin A. E. Aleksei, Petrov S. A. Stanislav Aleksandrovich, Bodenko V. V. Vitalina Vasiljevna, Larkina M. S. Mariya Sergeevna, Plotnikov E. V. Evgeny Vladimirovich, Yuldasheva F. Sh. Feruza Sherzod kizi, Tretyakova (Tretjyakova) M. S. Maria Sergeevna, Bezverkhniaia E. A. Ekaterina Aleksandrovna, Zyk N. Yu. Nikolai, Stasyuk (Stasiuk) E. S. Elena Sergeyevna, Zelchan (Zeltchan) R. V. Roman Vladimirovich, Mazhuga A. G. Aleksandr Georgievich, Tolmachev V. M. Vladimir Maksimilianovich, Orlova A. M. Anna Markovna, Beloglazkina E. K. Elena Kimovna, Yusubov M. S. Mekhman Suleiman-Ogly (Suleimanovich)
Riassunto:Title screen
177Lu-labeled small-molecule prostate-specific membrane antigen (PSMA) targeted tracers are therapeutic agents for metastatic castration-resistant prostate cancer. Optimizing molecular design holds the potential to further enhance the pharmacokinetic properties of PSMA-targeted agents while preserving their potent therapeutic effects. In this study, six novel N-[N-[(S)-1,3-dicarboxypropyl]carbamoyl]-(S)-L-lysine (DCL) urea-based PSMA ligand 2,2′,2″,2‴-(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrayl)tetraacetic acid conjugates were synthesized. These conjugates feature polypeptide linkers containing the Phe-Phe peptide sequence and an aromatic fragment at the ε-NH-Lys group of the DCL fragment. The synthesis yielded products with satisfactory yields ranging from 60% to 72%, paving the way for their preclinical evaluation. The labeling of the new variants of urea-based PSMA inhibitors provided a radiochemical yield of over 95%. The 177Lu-labeled conjugates demonstrated specific and moderate affinity binding to PSMA-expressing human cancer cells PC3-pip in vitro and specific accumulation in PSMA-expressing xenografts in vivo. Based on the results, both the lipophilicity and the type of substituent in the linker significantly influence the binding properties of the PSMA inhibitor and its biodistribution profile. Specifically, the studied variants containing a bromine substituent or a hydroxyl group introduced into the aromatic fragment of the phenylalanyl residue in DCL exhibit higher affinities to PSMA compared to variants with only a chlorine-substituted aromatic fragment or variants without any substituents. The [177Lu]Lu-13C with the bromine substituent was characterized by the highest activity accumulation in blood, salivary glands, muscle, bone, and gastrointestinal tract and had inasmuch as an unfavorable pharmacokinetic profile. The negative charge of the carboxyl group in the phenyl moiety of the [177Lu]Lu-13A variant has demonstrated a positive effect on reducing the retention of activity in the liver and the kidneys (the ratio of tumor to kidneys was 1.3-fold). Low accumulation in normal tissues in vivo indicates that this novel PSMA-targeting inhibitor is a promising radioligand.
Текстовый файл
Lingua:inglese
Pubblicazione: 2024
Soggetti:
Accesso online:https://doi.org/10.1021/acsptsci.4c00070
Natura: Elettronico Capitolo di libro
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=672770

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200 1 |a Synthesis and Preclinical Evaluation of Urea-Based Prostate-Specific Membrane Antigen-Targeted Conjugates Labeled with 177Lu  |f A. E. Machulkin, S. A. Petrov, V. Bodenko [et al.] 
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330 |a 177Lu-labeled small-molecule prostate-specific membrane antigen (PSMA) targeted tracers are therapeutic agents for metastatic castration-resistant prostate cancer. Optimizing molecular design holds the potential to further enhance the pharmacokinetic properties of PSMA-targeted agents while preserving their potent therapeutic effects. In this study, six novel N-[N-[(S)-1,3-dicarboxypropyl]carbamoyl]-(S)-L-lysine (DCL) urea-based PSMA ligand 2,2′,2″,2‴-(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrayl)tetraacetic acid conjugates were synthesized. These conjugates feature polypeptide linkers containing the Phe-Phe peptide sequence and an aromatic fragment at the ε-NH-Lys group of the DCL fragment. The synthesis yielded products with satisfactory yields ranging from 60% to 72%, paving the way for their preclinical evaluation. The labeling of the new variants of urea-based PSMA inhibitors provided a radiochemical yield of over 95%. The 177Lu-labeled conjugates demonstrated specific and moderate affinity binding to PSMA-expressing human cancer cells PC3-pip in vitro and specific accumulation in PSMA-expressing xenografts in vivo. Based on the results, both the lipophilicity and the type of substituent in the linker significantly influence the binding properties of the PSMA inhibitor and its biodistribution profile. Specifically, the studied variants containing a bromine substituent or a hydroxyl group introduced into the aromatic fragment of the phenylalanyl residue in DCL exhibit higher affinities to PSMA compared to variants with only a chlorine-substituted aromatic fragment or variants without any substituents. The [177Lu]Lu-13C with the bromine substituent was characterized by the highest activity accumulation in blood, salivary glands, muscle, bone, and gastrointestinal tract and had inasmuch as an unfavorable pharmacokinetic profile. The negative charge of the carboxyl group in the phenyl moiety of the [177Lu]Lu-13A variant has demonstrated a positive effect on reducing the retention of activity in the liver and the kidneys (the ratio of tumor to kidneys was 1.3-fold). Low accumulation in normal tissues in vivo indicates that this novel PSMA-targeting inhibitor is a promising radioligand. 
336 |a Текстовый файл 
461 1 |t ACS Pharmacology & Translational Science  |c Washington  |n ACS Publications 
463 1 |t Vol. 7, iss. 5  |v P. 1457–1473  |d 2024 
610 1 |a труды учёных ТПУ 
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701 1 |a Machulkin  |b A. E.  |g Aleksei 
701 1 |a Petrov  |b S. A.  |g Stanislav Aleksandrovich 
701 1 |a Bodenko  |b V. V.  |c pharmacist  |c engineer at Tomsk Polytechnic University  |f 1997-  |g Vitalina Vasiljevna  |9 88553 
701 1 |a Larkina  |b M. S.  |g Mariya Sergeevna  |f 1984-  |c pharmacist  |c Professor; Senior Researcher of the Tomsk Polytechnic University, Doctor of Pharmaceutical Sciences  |9 22417 
701 1 |a Plotnikov  |b E. V.  |c chemist  |c Associate Professor of Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1983-  |g Evgeny Vladimirovich  |9 16417 
701 1 |a Yuldasheva  |b F. Sh.  |g Feruza Sherzod kizi 
701 1 |a Tretyakova (Tretjyakova)  |b M. S.  |c Medical technology specialist  |c Research Engineer of Tomsk Polytechnic University  |f 1994-  |g Maria Sergeevna  |9 22127 
701 1 |a Bezverkhniaia  |b E. A.  |c pharmacist  |c Research Engineer Tomsk Polytechnic University  |f 1994-  |g Ekaterina Aleksandrovna  |9 22467 
701 1 |a Zyk  |b N. Yu.  |g Nikolai 
701 1 |a Stasyuk (Stasiuk)  |b E. S.  |c Specialist in the field of nuclear power engineering  |c Researcher of Tomsk Polytechnic University, Candidate of technical sciences  |f 1978-  |g Elena Sergeyevna  |9 16555 
701 1 |a Zelchan (Zeltchan)  |b R. V.  |c specialist in the field of medical technology  |c Researcher of the Tomsk Polytechnic University, Candidate of Medical Sciences  |f 1984-  |g Roman Vladimirovich  |9 17728 
701 1 |a Mazhuga  |b A. G.  |g Aleksandr Georgievich 
701 1 |a Tolmachev  |b V. M.  |c specialist in the field of medical technology  |c Director of the Research Center "Oncoteranostika", Tomsk Polytechnic University, Ph.D  |f 1961-  |g Vladimir Maksimilianovich  |9 22210 
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701 1 |a Yusubov  |b M. S.  |c chemist  |c Professor of Tomsk Polytechnic University, Doctor of chemical sciences  |f 1961-  |g Mekhman Suleiman-Ogly (Suleimanovich)  |9 15928 
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