Identification of a PET Radiotracer for Imaging of the Folate Receptor-α: A Potential Tool to Select Patients for Targeted Tumor Therapy
The aim of this study was to identify a folate receptor-α (FRα)-selective PET agent potentially suitable for the selection of patients who might profit from FRα-targeted therapies. The 6 and 6 isomers of F-aza-5-methyltetrahydrofolate (MTHF) were assessed regarding their binding to FRα and FRβ, expr...
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Published in | Journal of Nuclear Medicine Vol. 62; no. 10; pp. 1475 - 1481 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Society of Nuclear Medicine
01.10.2021
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Subjects | |
Online Access | Get full text |
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Summary: | The aim of this study was to identify a folate receptor-α (FRα)-selective PET agent potentially suitable for the selection of patients who might profit from FRα-targeted therapies. The 6
and 6
isomers of
F-aza-5-methyltetrahydrofolate (MTHF) were assessed regarding their binding to FRα and FRβ, expressed on cancer and inflammatory cells, respectively, and compared with
F-AzaFol, the folic acid-based analog.
FR selectivity was investigated using FRα-transfected (RT16) and FRβ-transfected (D4) CHO cells. The cell uptake of
F-folate tracers was investigated, and receptor-binding affinities were determined with the nonradioactive analogs. In vitro autoradiography of the
F-folate tracers was performed using RT16 and D4 tissue sections. Biodistribution studies and PET/CT imaging of the radiotracers were performed on mice bearing RT16 and D4 xenografts.
The uptake of
F-6
-aza-5-MTHF was high when using RT16 cells (62% ± 10% of added activity) but much lower when using D4 cells (5% ± 2%). The FRα selectivity of
F-6
-aza-5-MTHF was further demonstrated by its approximately 43-fold higher binding affinity to FRα (half-maximal inhibitory concentration [IC
], 1.8 ± 0.1 nM) than to FRβ (IC
, 77 ± 27 nM). The uptake of
F-6
-aza-5-MTHF and
F-AzaFol was equal in both cell lines (52%-70%), with similar affinities to FRα (IC
, 2.1 ± 0.4 nM and 0.6 ± 0.3 nM, respectively) and FRβ (0.8 ± 0.2 nM and 0.3 ± 0.1 nM, respectively). The autoradiography signal obtained with
F-6
-aza-5-MTHF was 11-fold more intense for RT16 than for D4 tissue sections. Biodistribution data showed high uptake of
F-6
-aza-5-MTHF in RT16 xenografts (81% ± 20% injected activity per gram [IA]/g 1 h after injection) but significantly lower accumulation in D4 xenografts (7.3% ± 2.1% IA/g 1 h after injection), which was also visualized using PET. The uptake of
F-6
-aza-5-MTHF and
F-AzaFol was similar in RT16 (53% ± 10% IA/g and 45% ± 2% IA/g, respectively) and D4 xenografts (77% ± 10% IA/g and 52% ± 7% IA/g, respectively).
This study demonstrated FRα selectivity for
F-6
-aza-5-MTHF but not for
F-6
-aza-5-MTHF or
F-AzaFol. This characteristic, together with its favorable tissue distribution, makes
F-6
-aza-5-MTHF attractive for clinical translation to enable detection of FRα-positive cancer while preventing undesired accumulation in FRβ-expressing inflammatory cells. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Published online January 15, 2021. |
ISSN: | 0161-5505 1535-5667 1535-5667 2159-662X |
DOI: | 10.2967/jnumed.120.255760 |