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001-es BibID:BIBFORM057386
Első szerző:Máté Gábor (gyógyszerész)
Cím:In vivo imaging of Aminopeptidase N (CD13) receptors in experimental renal tumors using the novel radiotracer 68Ga-NOTA-c(NGR) / Gábor Máté, István Kertész, Kata Nóra Enyedi, Gábor Mezo, János Angyal, Nikolett Vasas, Adrienn Kis, Éva Szabó, Miklós Emri, Tamás Bíró, László Galuska, György Trencsényi
Dátum:2015
ISSN:0928-0987
Megjegyzések:Purpose: Aminopeptidase N (APN/CD13) plays an important role in tumor neoangiogenic process and the development of metastases. Furthermore, it may serve as a potential target for cancer diagnosis and therapy. Previous studies have already shown that asparagine-glycine-arginine (NGR) peptides specifically bind to APN/CD13. The aim of the study was to synthesize and investigate the APN/CD13 specificity of a novel 68Ga-labeled NOTA-c(NGR) molecule in vivo using miniPET. Methods: c[KNGRE]-NH2 peptide was conjugated with p-SCN-Bn-NOTA and was labeled with Ga-68 ( 68Ga-NOTA-c(NGR)). Orthotopic and heterotopic transplanted mesoblastic nephroma (NeDe) bearing Fischer-344 rats were prepared, on which biodistribution studies and miniPET scans were performed for both 68Ga-NOTA-c(NGR) and amb3 integrin selective 68Ga-NODAGA-[c(RGD)]2 tracers. APN/CD13 receptor expression of NeDe tumors and metastases was analyzed by western blot. Results: 68Ga-NOTA-c(NGR) was produced with high specific activity (5.13-5.92 GBq/lmol) and with excellent radiochemical purity (95%<), at all cases. Biodistribution studies in normal rats showed that uptake of the 68Ga-NOTA-c(NGR) was significantly (p 6 0.05) lower in abdominal organs in comparison with 68Ga-NODAGA-[c(RGD)]2. Both radiotracers were mainly excreted from the kidney. In NeDe tumor bearing rats higher 68Ga-NOTA-c(NGR) accumulation was found in the tumors than that of the 68Ga-NODAGA-[c(RGD)]2. Using orthotopic transplantation, metastases were developed which showed specific 68Ga-NOTA-c(NGR) uptake. Western blot analysis confirmed the presence of APN/CD13 expression in NeDe tumors and metastases.
Tárgyszavak:Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Megjelenés:European Journal Of Pharmaceutical Sciences. - 69 (2015), p. 61-71. -
További szerzők:Kertész István (1966-) (vegyész) Enyedi Kata Nóra (1987-) (vegyész) Mező Gábor (1959-) (vegyész) Angyal János (1962-) (fogszakorvos) Molnárné Vasas Nikolett (1987-) (élettanász) Kis Adrienn (1991-) (molekuláris biológus) Szabó Éva Emri Miklós (1962-) (fizikus) Bíró Tamás (1968-) (élettanász) Galuska László (1946-) (belgyógyász, izotópdiagnoszta) Trencsényi György (1978-) (biológus, biokémikus, molekuláris biológus)
Pályázati támogatás:TÁMOP-4.2.4.A/2-11/1-2012-0001
TÁMOP
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001-es BibID:BIBFORM102628
035-os BibID:(WOS)000818925800013 (Scopus)85132685973
Első szerző:Péli-Szabó Judit (vegyész)
Cím:In Vivo Imaging of Neo-angiogenesis of Transplanted Metastases in Subrenal Capsule Assay Induced Rat Model / Judit P. Szabo, Noemi Denes, Viktoria Arato, Szilvia Racz, Adrienn Kis, Gabor Opposits, Zita Kepes, Istvan Hajdu, Istvan Joszai, Miklos Emri, Istvan Kertesz, Gabor Mezo, Gyorgy Trencsenyi
Dátum:2022
ISSN:0258-851X
Megjegyzések:Abstract Background/Aim: Changes in the expression of neo-angiogenic molecules in the primary tumor and its metastases may significantly affect the efficacy of therapies. The aim of this study was to evaluate the alterations in aminopeptidase N (APN/CD13) and ?v?3 integrin receptor expression in serially transplanted mesoblastic nephroma tumor (Ne/De) metastases using 68Gallium (68Ga)-labeled NOTA-cNGR and NODAGA-RGD radiotracers and preclinical positron emission tomography (PET) imaging. Materials and Methods: Primary and metastatic mesoblastic nephroma (Ne/De) tumors were induced by subrenal capsule assay (SRCA) in Fischer-344 rats. In vivo PET imaging experiments were performed 8?1 days after the SRCA surgery using intravenously injected 68Ga-NOTA-c(NGR), 68Ga-NODAGA-RGD, and [18F]FDG radiotracers. Results: Among the examined neo-angiogenic molecules, the expression of ?v?3 integrin in the tumors was significantly lower than that of APN/CD13. This observation was confirmed by the PET data analysis, where a 2-6-fold higher APN/CD13-specific 68Ga-NOTA-cNGR accumulation was observed in both primary malignancies and metastases. However, a steadily increased accumulation of [18F]FDG, 68Ga-NODAGA-RGD, and 68Ga-NOTA-cNGR was observed in the tumors growing under the renal capsule and in the metastatic parathymic lymph nodes during serial transplantations. The observed increase in 68Ga- NOTA-cNGR accumulation during serial transplantations correlated well with the western blot analysis, where APN/CD13 protein levels were also elevated in the metastatic parathymic lymph nodes. Conclusion: The observed increase in glucose metabolism and the up-regulated expression of ?v?3 integrin and APN/CD13 during serial transplantations of metastases may indicate enhanced malignancy.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Aminopeptidase N
angiogenesis
68Ga-NOTA-c(NGR)
metastasis
NGR peptide
positron emission tomography
Megjelenés:In Vivo. - 36 : 4 (2022), p. 1667-1675. -
További szerzők:Dénes Noémi (1992-) (vegyész) Arató Viktória Zsófia (1989-) (gyógyszerész) Rácz Szilvia (1989-) (molekulársi biológus) Kis Adrienn (1991-) (molekuláris biológus) Opposits Gábor (1974-) (fizikus, szoftver fejlesztő) Képes Zita (1991-) (orvos) Hajdu István (1981-) (vegyész) Jószai István (1978-) (vegyész) Emri Miklós (1962-) (fizikus) Kertész István (1966-) (vegyész) Mező Gábor (1959-) (vegyész) Trencsényi György (1978-) (biológus, biokémikus, molekuláris biológus)
Pályázati támogatás:EFOP-3.6.3-VEKOP-162017-00009
Egyéb
NKFIH-K-119552
Egyéb
TKP2020-NKA-04
Egyéb
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DOI
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