Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer Imaging

It has been reported that dysregulation of microRNA-155 expression and function is associated with tumorigenesis, growth, tumor subtypes, invasion, and poor survival rates. Peptide nucleic acid (PNA), an artificially synthesized nucleic acid mimic, has been applied for molecular diagnosis. In this s...

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Main Authors: Yaqun Jiang MD, Yongkang Gai PhD, Yu Long MD, Qingyao Liu PhD, Chunbao Liu MD, PhD, Yongxue Zhang MD, Xiaoli Lan MD, PhD
Format: Article
Language:English
Published: SAGE Publishing 2020-06-01
Series:Molecular Imaging
Online Access:https://doi.org/10.1177/1536012120916124
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author Yaqun Jiang MD
Yongkang Gai PhD
Yu Long MD
Qingyao Liu PhD
Chunbao Liu MD, PhD
Yongxue Zhang MD
Xiaoli Lan MD, PhD
author_facet Yaqun Jiang MD
Yongkang Gai PhD
Yu Long MD
Qingyao Liu PhD
Chunbao Liu MD, PhD
Yongxue Zhang MD
Xiaoli Lan MD, PhD
author_sort Yaqun Jiang MD
collection DOAJ
description It has been reported that dysregulation of microRNA-155 expression and function is associated with tumorigenesis, growth, tumor subtypes, invasion, and poor survival rates. Peptide nucleic acid (PNA), an artificially synthesized nucleic acid mimic, has been applied for molecular diagnosis. In this study, a PNA sequence that undergoes complementary binding to miR-155 was labeled with 99m Tc to evaluate whether the tracer could visualize the expression of miR-155 in breast cancer. Both antisense PNA (anti-PNA, fully complementary bound to human mature miR-155 , referred to as “anti-PNA-155”) and mismatched PNA (referred to as “mis-PNA”) single strands containing 23-mer were synthesized. The relative expression of miR-155 in MCF-7 cells and tumors was higher than that in MDA-MB-231 cells and tumors. Single-photon emission computed tomography (SPECT) scan showed that radioactivity mainly accumulated in kidney. MCF-7 tumors, but not MDA-MB-231 tumors, were clearly visualized after [ 99m Tc]anti-PNA-155 injection. MCF-7 tumors were less visible when coinjected with 100-fold excess of anti-PNA-155 or injected with [ 99m Tc]mis-PNA, which suggested specific binding. Biodistribution study results were consistent with SPECT imaging. We successfully demonstrated that [ 99m Tc]anti-PNA-155 could visualize miR-155 expression in vivo, suggesting it may be a promising probe applied in breast cancer.
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spelling doaj-art-d00ef43246ae43dbb9b808f01465e9702025-02-03T10:07:51ZengSAGE PublishingMolecular Imaging1536-01212020-06-011910.1177/1536012120916124Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer ImagingYaqun Jiang MD0Yongkang Gai PhD1Yu Long MD2Qingyao Liu PhD3Chunbao Liu MD, PhD4Yongxue Zhang MD5Xiaoli Lan MD, PhD6 Hubei Province Key Laboratory of Molecular Imaging, Wuhan, China Hubei Province Key Laboratory of Molecular Imaging, Wuhan, China Hubei Province Key Laboratory of Molecular Imaging, Wuhan, China Hubei Province Key Laboratory of Molecular Imaging, Wuhan, China Department of Nuclear Medicine, the Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China Hubei Province Key Laboratory of Molecular Imaging, Wuhan, China Hubei Province Key Laboratory of Molecular Imaging, Wuhan, ChinaIt has been reported that dysregulation of microRNA-155 expression and function is associated with tumorigenesis, growth, tumor subtypes, invasion, and poor survival rates. Peptide nucleic acid (PNA), an artificially synthesized nucleic acid mimic, has been applied for molecular diagnosis. In this study, a PNA sequence that undergoes complementary binding to miR-155 was labeled with 99m Tc to evaluate whether the tracer could visualize the expression of miR-155 in breast cancer. Both antisense PNA (anti-PNA, fully complementary bound to human mature miR-155 , referred to as “anti-PNA-155”) and mismatched PNA (referred to as “mis-PNA”) single strands containing 23-mer were synthesized. The relative expression of miR-155 in MCF-7 cells and tumors was higher than that in MDA-MB-231 cells and tumors. Single-photon emission computed tomography (SPECT) scan showed that radioactivity mainly accumulated in kidney. MCF-7 tumors, but not MDA-MB-231 tumors, were clearly visualized after [ 99m Tc]anti-PNA-155 injection. MCF-7 tumors were less visible when coinjected with 100-fold excess of anti-PNA-155 or injected with [ 99m Tc]mis-PNA, which suggested specific binding. Biodistribution study results were consistent with SPECT imaging. We successfully demonstrated that [ 99m Tc]anti-PNA-155 could visualize miR-155 expression in vivo, suggesting it may be a promising probe applied in breast cancer.https://doi.org/10.1177/1536012120916124
spellingShingle Yaqun Jiang MD
Yongkang Gai PhD
Yu Long MD
Qingyao Liu PhD
Chunbao Liu MD, PhD
Yongxue Zhang MD
Xiaoli Lan MD, PhD
Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer Imaging
Molecular Imaging
title Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer Imaging
title_full Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer Imaging
title_fullStr Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer Imaging
title_full_unstemmed Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer Imaging
title_short Application and Evaluation of [Tc]-Labeled Peptide Nucleic Acid Targeting in Breast Cancer Imaging
title_sort application and evaluation of tc labeled peptide nucleic acid targeting in breast cancer imaging
url https://doi.org/10.1177/1536012120916124
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