Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.

There is an increasing need to characterize biological processes for early prediction and monitoring of response to endocrine therapy in breast cancer using multiple positron emission tomography (PET) imaging probes. However, use of more than two PET tracers in a single clinical trial is quite chall...

Full description

Bibliographic Details
Main Authors: SiMin He, MingWei Wang, ZhongYi Yang, JianPing Zhang, YongPing Zhang, JianMin Luo, YingJian Zhang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4965120?pdf=render
_version_ 1818526346095099904
author SiMin He
MingWei Wang
ZhongYi Yang
JianPing Zhang
YongPing Zhang
JianMin Luo
YingJian Zhang
author_facet SiMin He
MingWei Wang
ZhongYi Yang
JianPing Zhang
YongPing Zhang
JianMin Luo
YingJian Zhang
author_sort SiMin He
collection DOAJ
description There is an increasing need to characterize biological processes for early prediction and monitoring of response to endocrine therapy in breast cancer using multiple positron emission tomography (PET) imaging probes. However, use of more than two PET tracers in a single clinical trial is quite challenging. In this study we carried out a longitudinal investigation of 18F-FES, 18F-FDG, and 18F-FMISO PET imaging probes for early prediction and monitoring of response to endocrine therapy in a mouse xenograft model of estrogen receptor (ER)-positive breast cancer.ER+ human breast cancer ZR-75-1 models were established in female mice that were then randomly assigned to a treatment (fulvestrant, 5.0 mg/week for 21 days) or vehicle group. Micro-PET/CT imaging with 18F-FES, 18F-FDG, and 18F-FMISO was performed on days 0, 3, 14, and 21 after treatment. The uptake value (percentage injected dose per gram, %ID/g) for each probe in tumor (T) tissue and contralateral muscle (M) was measured for quantitative analysis and T/M calculation. Tumor volume was measured to record tumor growth at each time point. Tumor tissues were sampled for immunohistochemical staining of ER expression. Correlations for tumor volume and ERα levels with uptake data for the probe were tested.Uptake data for 18F-FES in ZR-75-1 tumor tissues corresponded well with tumor response to endocrine therapy, but not for 18F-FDG and 18F-FMISO, according to longitudinal micro-PET/CT imaging and quantitative correlation analysis. There was a significant positive correlation between 18F-FES uptake and ER levels (%ID/gmax r2 = 0.76, P< 0.05; T/M r2 = 0.82, P<0.05). Notably, 18F-FES uptake on day 3 was significantly correlated with the day 21/baseline tumor volume ratio (%ID/gmax r2 = 0.74, P < 0.05; T/M r2 = 0.78, P < 0.05).Comparison of 18F-FES, 18F-FDG, and 18F-FMISO probes revealed that 18F-FES PET/CT molecular imaging can provide a precise early prediction of tumor response to endocrine therapy in ER+ breast cancer in a ZR-75-1 xenograft model. This molecular imaging strategy with 18F-FES PET/CT will be useful in evaluating the efficacy of endocrine therapies and in developing new endocrine drugs.
first_indexed 2024-12-11T06:21:43Z
format Article
id doaj.art-fdd69c32a83a4baaa2803ba603c3527a
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-11T06:21:43Z
publishDate 2016-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-fdd69c32a83a4baaa2803ba603c3527a2022-12-22T01:17:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01117e015991610.1371/journal.pone.0159916Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.SiMin HeMingWei WangZhongYi YangJianPing ZhangYongPing ZhangJianMin LuoYingJian ZhangThere is an increasing need to characterize biological processes for early prediction and monitoring of response to endocrine therapy in breast cancer using multiple positron emission tomography (PET) imaging probes. However, use of more than two PET tracers in a single clinical trial is quite challenging. In this study we carried out a longitudinal investigation of 18F-FES, 18F-FDG, and 18F-FMISO PET imaging probes for early prediction and monitoring of response to endocrine therapy in a mouse xenograft model of estrogen receptor (ER)-positive breast cancer.ER+ human breast cancer ZR-75-1 models were established in female mice that were then randomly assigned to a treatment (fulvestrant, 5.0 mg/week for 21 days) or vehicle group. Micro-PET/CT imaging with 18F-FES, 18F-FDG, and 18F-FMISO was performed on days 0, 3, 14, and 21 after treatment. The uptake value (percentage injected dose per gram, %ID/g) for each probe in tumor (T) tissue and contralateral muscle (M) was measured for quantitative analysis and T/M calculation. Tumor volume was measured to record tumor growth at each time point. Tumor tissues were sampled for immunohistochemical staining of ER expression. Correlations for tumor volume and ERα levels with uptake data for the probe were tested.Uptake data for 18F-FES in ZR-75-1 tumor tissues corresponded well with tumor response to endocrine therapy, but not for 18F-FDG and 18F-FMISO, according to longitudinal micro-PET/CT imaging and quantitative correlation analysis. There was a significant positive correlation between 18F-FES uptake and ER levels (%ID/gmax r2 = 0.76, P< 0.05; T/M r2 = 0.82, P<0.05). Notably, 18F-FES uptake on day 3 was significantly correlated with the day 21/baseline tumor volume ratio (%ID/gmax r2 = 0.74, P < 0.05; T/M r2 = 0.78, P < 0.05).Comparison of 18F-FES, 18F-FDG, and 18F-FMISO probes revealed that 18F-FES PET/CT molecular imaging can provide a precise early prediction of tumor response to endocrine therapy in ER+ breast cancer in a ZR-75-1 xenograft model. This molecular imaging strategy with 18F-FES PET/CT will be useful in evaluating the efficacy of endocrine therapies and in developing new endocrine drugs.http://europepmc.org/articles/PMC4965120?pdf=render
spellingShingle SiMin He
MingWei Wang
ZhongYi Yang
JianPing Zhang
YongPing Zhang
JianMin Luo
YingJian Zhang
Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.
PLoS ONE
title Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.
title_full Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.
title_fullStr Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.
title_full_unstemmed Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.
title_short Comparison of 18F-FES, 18F-FDG, and 18F-FMISO PET Imaging Probes for Early Prediction and Monitoring of Response to Endocrine Therapy in a Mouse Xenograft Model of ER-Positive Breast Cancer.
title_sort comparison of 18f fes 18f fdg and 18f fmiso pet imaging probes for early prediction and monitoring of response to endocrine therapy in a mouse xenograft model of er positive breast cancer
url http://europepmc.org/articles/PMC4965120?pdf=render
work_keys_str_mv AT siminhe comparisonof18ffes18ffdgand18ffmisopetimagingprobesforearlypredictionandmonitoringofresponsetoendocrinetherapyinamousexenograftmodeloferpositivebreastcancer
AT mingweiwang comparisonof18ffes18ffdgand18ffmisopetimagingprobesforearlypredictionandmonitoringofresponsetoendocrinetherapyinamousexenograftmodeloferpositivebreastcancer
AT zhongyiyang comparisonof18ffes18ffdgand18ffmisopetimagingprobesforearlypredictionandmonitoringofresponsetoendocrinetherapyinamousexenograftmodeloferpositivebreastcancer
AT jianpingzhang comparisonof18ffes18ffdgand18ffmisopetimagingprobesforearlypredictionandmonitoringofresponsetoendocrinetherapyinamousexenograftmodeloferpositivebreastcancer
AT yongpingzhang comparisonof18ffes18ffdgand18ffmisopetimagingprobesforearlypredictionandmonitoringofresponsetoendocrinetherapyinamousexenograftmodeloferpositivebreastcancer
AT jianminluo comparisonof18ffes18ffdgand18ffmisopetimagingprobesforearlypredictionandmonitoringofresponsetoendocrinetherapyinamousexenograftmodeloferpositivebreastcancer
AT yingjianzhang comparisonof18ffes18ffdgand18ffmisopetimagingprobesforearlypredictionandmonitoringofresponsetoendocrinetherapyinamousexenograftmodeloferpositivebreastcancer