Abstract | BACKGROUND: METHODS: 18F-FES uptake in vivo was evaluated in ZR-75-1 tumor-bearing mice, using MCF-7 tumor-bearing mice as a positive control. Competitive inhibition experiment was also performed, using ER down-regulator fulvestrant. Biodistribution of 18F-FES was observed in ZR-75-1 breast tumor-bearing mice scanning by 18F-FES-PET/CT in vivo and γ counter ex vivo. The expression of ER was also determined by immunohistochemistry. An abnormal toxicity test was performed in ICR male mice whose behavior and vital signs were observed within 48 hours of 18F-FES injection. OLINDA/EXM 2.0 software was used to calculate the absorbed doses of adult female body phantoms. RESULTS: There was no significant difference in FES uptake between ZR-75-1 and MCF-7 tumor-bearing mice. Intervention with fulvestrant decreased the uptake of 18F-FES. Biodistribution studies demonstrated that the uptake of 18F-FES was high in the liver and kidneys but low in the brain. Other than excretory organs, the uptake of 18F-FES in ER-positive breast tumors was significantly higher than in ER-negative tissues. The estimated human effective dose was 0.016 mSv/MBq for the adult female body model. CONCLUSIONS: The 18F-FES tracer could have suitable properties for imaging ER-positive breast tumors. It may provide an important evidence for individualized treatment of patients with breast cancer.
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Authors | Ziteng Ding, Xudang Xu, Tiannv Li, Jia Wang, Jin Sun, Lijun Tang |
Journal | Translational cancer research
(Transl Cancer Res)
Vol. 10
Issue 3
Pg. 1430-1438
(Mar 2021)
ISSN: 2219-6803 [Electronic] China |
PMID | 35116468
(Publication Type: Journal Article)
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Copyright | 2021 Translational Cancer Research. All rights reserved. |