Comparative Preclinical Evaluation of the Tumor-Targeting Properties of Radioiodine and Technetium-Labeled Designed Ankyrin Repeat Proteins for Imaging of Epidermal Growth Factor Receptor Expression in Malignant Tumors; International Journal of Molecular Sciences; Vol. 26, iss. 21

Dades bibliogràfiques
Parent link:International Journal of Molecular Sciences.— .— Basel: MDPI AG
Vol. 26, iss. 21.— 2025.— Article number 10609, 22 p.
Altres autors: Larkina M. S. Mariya Sergeevna, Yanovich G. Gleb, Hasnowo L. A. Lutfi Aditya (Hasnowo Lutfi Aditya, Varvashenya R. N. Ruslan Nikolaevich, Yuldasheva F. Sh. Feruza Sherzod kizi, Tretyakova (Tretjyakova) M. S. Maria Sergeevna, Plotnikov E. V. Evgeny Vladimirovich, Zelchan (Zeltchan) R. V. Roman Vladimirovich, Shulga (Schulga) A. A. Aleksey Anatolievich, Konovalova E. V. Elena Valerjevna, Ziganshin R. Rustam, Belousov M. V. Mikhail Valerievich, Tolmachev V. Vladimir, Deev S. M. Sergey Mikhaylovich
Sumari:Title screen
Radionuclide molecular imaging of epidermal growth factor receptor (EGFR) expression might permit the selection of patients for EGFR-targeting therapies. Designed ankyrin repeat protein (DARPin) E01 with a high affinity to the ectodomain III of the EGFR is a possible EGFR imaging probe. The goal of this study was to evaluate the potential of radiolabeled DARPin E01 for in vivo imaging of EGFR. DARPin E01 containing the (HE)3-tag was site-specifically labeled with a residualizing 99mTc (using 99mTc]Tc(CO)3). Two methods providing non-residualizing 123I labels, direct electrophilic radioiodination and indirect radioiodination using [123I]I-para-iodobenzoate (PIB), were tested. [99mTc]Tc-(HE)3-E01 and [123I]I-(HE)3-E01-PIB preserved specific binding to EGFR-expressing cells and affinity in the single-digit nanomolar range. Direct labeling with 123I resulted in a substantial loss of binding. In vitro cellular processing studies showed that both [99mTc]Tc-(HE)3-E01 and [123I]I-(HE)3-E01-PIB had rapid binding and relatively slow internalization. Evaluation of [99mTc]Tc-(HE)3-E01 biodistribution in normal CD1 mice showed that its hepatic uptake was non-saturable, suggesting that this tracer does not bind to murine EGFR. A side-by-side comparison of biodistribution and tumor targeting of [99mTc]Tc-(HE)3-E01 and [123I]I-(HE)3-E01-PIB was performed in Nu/j mice bearing EGFR-positive A-431 and EGFR-negative Ramos human cancer xenografts. Both radiolabeled DARPins demonstrated EGFR-specific tumor uptake. However, [123I]I-(HE)3-E01-PIB had appreciably lower uptake in normal organs compared to [99mTc]Tc-(HE)3-E01, which provided significantly (p < 0.05) higher tumor-to-organ ratios. Gamma-camera imaging confirmed that [123I]I-(HE)3-E01-PIB demonstrated a higher imaging contrast in preclinical models than [99mTc]Tc-(HE)3-E01. In conclusion, DARPin (HE)3-E01 labeled using a non-residualizing [123I]I-para-iodobenzoate (PIB) label is the preferred radiotracer for in vivo imaging of EGFR expression in cancer
Текстовый файл
Idioma:anglès
Publicat: 2025
Matèries:
Accés en línia:https://doi.org/10.3390/ijms262110609
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=684383

MARC

LEADER 00000naa0a2200000 4500
001 684383
005 20260311104142.0
090 |a 684383 
100 |a 20260122d2025 k||y0rusy50 ca 
101 1 |a eng 
102 |a CH 
135 |a drcn ---uucaa 
181 0 |a i   |b  e  
182 0 |a b 
183 0 |a cr  |2 RDAcarrier 
200 1 |a Comparative Preclinical Evaluation of the Tumor-Targeting Properties of Radioiodine and Technetium-Labeled Designed Ankyrin Repeat Proteins for Imaging of Epidermal Growth Factor Receptor Expression in Malignant Tumors  |f Mariia Larkina, Gleb Yanovich, Lutfi Aditya Hasnowo [et al.] 
203 |a Текст  |b визуальный  |c электронный 
283 |a online_resource  |2 RDAcarrier 
300 |a Title screen 
320 |a References: 64 tit 
330 |a Radionuclide molecular imaging of epidermal growth factor receptor (EGFR) expression might permit the selection of patients for EGFR-targeting therapies. Designed ankyrin repeat protein (DARPin) E01 with a high affinity to the ectodomain III of the EGFR is a possible EGFR imaging probe. The goal of this study was to evaluate the potential of radiolabeled DARPin E01 for in vivo imaging of EGFR. DARPin E01 containing the (HE)3-tag was site-specifically labeled with a residualizing 99mTc (using 99mTc]Tc(CO)3). Two methods providing non-residualizing 123I labels, direct electrophilic radioiodination and indirect radioiodination using [123I]I-para-iodobenzoate (PIB), were tested. [99mTc]Tc-(HE)3-E01 and [123I]I-(HE)3-E01-PIB preserved specific binding to EGFR-expressing cells and affinity in the single-digit nanomolar range. Direct labeling with 123I resulted in a substantial loss of binding. In vitro cellular processing studies showed that both [99mTc]Tc-(HE)3-E01 and [123I]I-(HE)3-E01-PIB had rapid binding and relatively slow internalization. Evaluation of [99mTc]Tc-(HE)3-E01 biodistribution in normal CD1 mice showed that its hepatic uptake was non-saturable, suggesting that this tracer does not bind to murine EGFR. A side-by-side comparison of biodistribution and tumor targeting of [99mTc]Tc-(HE)3-E01 and [123I]I-(HE)3-E01-PIB was performed in Nu/j mice bearing EGFR-positive A-431 and EGFR-negative Ramos human cancer xenografts. Both radiolabeled DARPins demonstrated EGFR-specific tumor uptake. However, [123I]I-(HE)3-E01-PIB had appreciably lower uptake in normal organs compared to [99mTc]Tc-(HE)3-E01, which provided significantly (p < 0.05) higher tumor-to-organ ratios. Gamma-camera imaging confirmed that [123I]I-(HE)3-E01-PIB demonstrated a higher imaging contrast in preclinical models than [99mTc]Tc-(HE)3-E01. In conclusion, DARPin (HE)3-E01 labeled using a non-residualizing [123I]I-para-iodobenzoate (PIB) label is the preferred radiotracer for in vivo imaging of EGFR expression in cancer 
336 |a Текстовый файл 
461 1 |t International Journal of Molecular Sciences  |c Basel  |n MDPI AG 
463 1 |t Vol. 26, iss. 21  |v Article number 10609, 22 p.  |d 2025 
610 1 |a EGFR imaging 
610 1 |a DARPin E01 
610 1 |a radiolabeling 
610 1 |a technetium-99m 
610 1 |a iodine-123 
610 1 |a residualizing label 
610 1 |a non-residualizing label 
610 1 |a tumor targeting 
610 1 |a biodistribution 
610 1 |a SPECT imaging 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
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 Yanovich  |b G.  |c Pharmacist  |c engineer of Tomsk Polytechnic University  |f 1999-  |g Gleb  |9 89205 
701 1 |a Hasnowo  |b L. A.  |g Lutfi Aditya (Hasnowo Lutfi Aditya 
701 1 |a Varvashenya  |b R. N.  |c pharmacist  |c engineer at Tomsk Polytechnic University  |f 1997-  |g Ruslan Nikolaevich  |9 88559 
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 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 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 Shulga (Schulga)  |b A. A.  |c biologist  |c Researcher, Tomsk Polytechnic University, Candidate of Biological Sciences  |f 1960-  |g Aleksey Anatolievich  |9 22432 
701 1 |a Konovalova  |b E. V.  |c specialist in the field of chemical technology and biotechnology  |c engineer at Tomsk Polytechnic University  |f 1985-  |g Elena Valerjevna  |9 88562 
701 1 |a Ziganshin  |b R.  |g Rustam 
701 1 |a Belousov  |b M. V.  |c chemist  |c Professor of Tomsk Polytechnic University, Doctor of Pharmaceutical Sciences  |f 1963-  |g Mikhail Valerievich  |9 21924 
701 1 |a Tolmachev  |b V.  |g Vladimir 
701 1 |a Deev  |b S. M.  |c biologist  |c Leading Researcher, Tomsk Polytechnic University, Doctor of Biological Sciences  |f 1951-  |g Sergey Mikhaylovich  |9 20959 
801 0 |a RU  |b 63413507  |c 20260122 
850 |a 63413507 
856 4 0 |u https://doi.org/10.3390/ijms262110609  |z https://doi.org/10.3390/ijms262110609 
942 |c CF