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In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis
INTRODUCTION: Integrin αvβ6, which is upregulated in malignancies and remains absent or weak in normal tissue, is a promising target in molecular imaging therapeutics. In vivo imaging of integrin αvβ6 could therefore be valuable for early tumor detection and intraoperative guidance. METHODS: In this...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036820/ https://www.ncbi.nlm.nih.gov/pubmed/36968997 http://dx.doi.org/10.3389/fonc.2023.1070967 |
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author | Fan, Di Zhang, Chengkai Luo, Qi Li, Baowang Ai, Lin Li, Deling Jia, Wang |
author_facet | Fan, Di Zhang, Chengkai Luo, Qi Li, Baowang Ai, Lin Li, Deling Jia, Wang |
author_sort | Fan, Di |
collection | PubMed |
description | INTRODUCTION: Integrin αvβ6, which is upregulated in malignancies and remains absent or weak in normal tissue, is a promising target in molecular imaging therapeutics. In vivo imaging of integrin αvβ6 could therefore be valuable for early tumor detection and intraoperative guidance. METHODS: In this study, integrin αvβ6-targeting probe G2-SFLAP3 was labeled with near-infrared (NIR) dye Cy5.5 or radioisotope 68Ga. The resulting probes were evaluated in integrin αvβ6-positive A549 and αvβ6-negative H1703 xenograft mice models. RESULTS: The cellar uptake of G2-SFLAP3-Cy5.5 was consistent with the expression of integrin αvβ6. Both subcutaneous and brain metastatic A549 tumors could be clearly visualized by NIR fluorescent imaging of G2-SFLAP3-Cy5.5. A549 tumors demonstrated the highest G2-SFLAP3-Cy5.5 accumulation at 4h post-injection (p.i.) and remain detectable at 84h p.i. The fluorescent signal of G2-SFLAP3-Cy5.5 was significantly reduced in H1703 and A549-blocking groups. Consistently, small-animal PET imaging showed tumor-specific accumulation of 68Ga-DOTA-G2-SFLAP3. DISCUSSION: G2-SFLAP3 represents a promising agent for noninvasive imaging of non-small cell lung cancer (NSCLC) and brain metastases. |
format | Online Article Text |
id | pubmed-10036820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100368202023-03-25 In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis Fan, Di Zhang, Chengkai Luo, Qi Li, Baowang Ai, Lin Li, Deling Jia, Wang Front Oncol Oncology INTRODUCTION: Integrin αvβ6, which is upregulated in malignancies and remains absent or weak in normal tissue, is a promising target in molecular imaging therapeutics. In vivo imaging of integrin αvβ6 could therefore be valuable for early tumor detection and intraoperative guidance. METHODS: In this study, integrin αvβ6-targeting probe G2-SFLAP3 was labeled with near-infrared (NIR) dye Cy5.5 or radioisotope 68Ga. The resulting probes were evaluated in integrin αvβ6-positive A549 and αvβ6-negative H1703 xenograft mice models. RESULTS: The cellar uptake of G2-SFLAP3-Cy5.5 was consistent with the expression of integrin αvβ6. Both subcutaneous and brain metastatic A549 tumors could be clearly visualized by NIR fluorescent imaging of G2-SFLAP3-Cy5.5. A549 tumors demonstrated the highest G2-SFLAP3-Cy5.5 accumulation at 4h post-injection (p.i.) and remain detectable at 84h p.i. The fluorescent signal of G2-SFLAP3-Cy5.5 was significantly reduced in H1703 and A549-blocking groups. Consistently, small-animal PET imaging showed tumor-specific accumulation of 68Ga-DOTA-G2-SFLAP3. DISCUSSION: G2-SFLAP3 represents a promising agent for noninvasive imaging of non-small cell lung cancer (NSCLC) and brain metastases. Frontiers Media S.A. 2023-03-10 /pmc/articles/PMC10036820/ /pubmed/36968997 http://dx.doi.org/10.3389/fonc.2023.1070967 Text en Copyright © 2023 Fan, Zhang, Luo, Li, Ai, Li and Jia https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Fan, Di Zhang, Chengkai Luo, Qi Li, Baowang Ai, Lin Li, Deling Jia, Wang In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis |
title |
In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis |
title_full |
In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis |
title_fullStr |
In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis |
title_full_unstemmed |
In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis |
title_short |
In vivo evaluation of integrin αvβ6-targeting peptide in NSCLC and brain metastasis |
title_sort | in vivo evaluation of integrin αvβ6-targeting peptide in nsclc and brain metastasis |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036820/ https://www.ncbi.nlm.nih.gov/pubmed/36968997 http://dx.doi.org/10.3389/fonc.2023.1070967 |
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