Comparison of tumor‑targeting properties of directly and indirectly radioiodinated designed ankyrin repeat protein (DARPin) G3 variants for molecular imaging of HER2.


Journal

International journal of oncology
ISSN: 1791-2423
Titre abrégé: Int J Oncol
Pays: Greece
ID NLM: 9306042

Informations de publication

Date de publication:
04 2019
Historique:
received: 27 09 2018
accepted: 25 01 2019
pubmed: 11 4 2019
medline: 27 8 2019
entrez: 11 4 2019
Statut: ppublish

Résumé

Evaluation of human epidermal growth factor receptor 2 (HER2) expression levels in breast and gastroesophageal cancer is used for the stratification of patients for HER2‑targeting therapies. The use of radionuclide molecular imaging may facilitate such evaluation in a non‑invasive way. Designed ankyrin repeat proteins (DARPins) are engineered scaffold proteins with high potential as probes for radionuclide molecular imaging. DARPin G3 binds with high affinity to HER2 and may be used to visualize this important therapeutic target. Studies on other engineered scaffold proteins have demonstrated that selection of the optimal labeling approach improves the sensitivity and specificity of radionuclide imaging. The present study compared two methods of labeling G3, direct and indirect radioiodination, to select an approach providing the best imaging contrast. G3‑H6 was labeled with iodine‑124, iodine‑125 and iodine‑131 using a direct method. A novel construct bearing a C‑terminal cysteine, G3‑GGGC, was site‑specifically labeled using [125I]I‑iodo‑[(4‑hydroxyphenyl)ethyl]maleimide (HPEM). The two radiolabeled G3 variants preserved binding specificity and high affinity to HER2‑expressing cells. The specificity of tumor targeting in vivo was demonstrated. Biodistribution comparison of [131I]I‑G3‑H6 and [125I]I‑HPEM‑G3‑GGGC in mice, bearing HER2‑expressing SKOV3 xenografts, demonstrated an appreciable contribution of hepatobiliary excretion to the clearance of [125I]I‑HPEM‑G3‑GGGC and a decreased tumor uptake compared to [131I]I‑G3‑H6. The direct label provided higher tumor‑to‑blood and tumor‑to‑organ ratios compared with the indirect label at 4 h post‑injection. The feasibility of high contrast PET/CT imaging of HER2 expression in SKOV3 xenografts in mice using [124I]I‑G3‑H6 was demonstrated. In conclusion, direct radioiodination is the preferable approach for labeling DARPin G3 with iodine‑123 and iodine‑124 for clinical single photon emission computed tomography and positron emission tomography imaging.

Identifiants

pubmed: 30968147
doi: 10.3892/ijo.2019.4712
pmc: PMC6411343
doi:

Substances chimiques

Iodine Radioisotopes 0
Recombinant Proteins 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Comparative Study Journal Article

Langues

eng

Pagination

1209-1220

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Auteurs

Anzhelika Vorobyeva (A)

Department of Immunology, Genetics and Pathology, Uppsala University, SE 75185 Uppsala, Sweden.

Alexey Sсhulga (A)

Molecular Immunology Laboratory, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia.

Elena Konovalova (E)

Molecular Immunology Laboratory, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia.

Rezan Güler (R)

Department of Protein Science, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, SE 10691 Stockholm, Sweden.

Bogdan Mitran (B)

Department of Medicinal Chemistry, Uppsala University, SE 75183 Uppsala, Sweden.

Javad Garousi (J)

Department of Immunology, Genetics and Pathology, Uppsala University, SE 75185 Uppsala, Sweden.

Sara Rinne (S)

Department of Medicinal Chemistry, Uppsala University, SE 75183 Uppsala, Sweden.

John Löfblom (J)

Department of Protein Science, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institute of Technology, SE 10691 Stockholm, Sweden.

Anna Orlova (A)

Department of Medicinal Chemistry, Uppsala University, SE 75183 Uppsala, Sweden.

Sergey Deyev (S)

Molecular Immunology Laboratory, Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia.

Vladimir Tolmachev (V)

Department of Immunology, Genetics and Pathology, Uppsala University, SE 75185 Uppsala, Sweden.

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Classifications MeSH