Cargando…

Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts

Positron emission tomography (PET) imaging with [F-18]-fluoro-2-deoxy-D-glucose ((18)F-FDG) is extensively applied in clinical practice. However, in animal experiments, the application of clinical PET is difficult, due to limitations in sensitivity and spatial resolution. This study aimed to determi...

Descripción completa

Detalles Bibliográficos
Autores principales: XU, OU, LI, XIAOMING, SHAN, CHUNGUANG, YANG, XING, ZHANG, LIN, WANG, JINGMIAO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786834/
https://www.ncbi.nlm.nih.gov/pubmed/24137257
http://dx.doi.org/10.3892/etm.2013.1200
_version_ 1782477782511517696
author XU, OU
LI, XIAOMING
SHAN, CHUNGUANG
YANG, XING
ZHANG, LIN
WANG, JINGMIAO
author_facet XU, OU
LI, XIAOMING
SHAN, CHUNGUANG
YANG, XING
ZHANG, LIN
WANG, JINGMIAO
author_sort XU, OU
collection PubMed
description Positron emission tomography (PET) imaging with [F-18]-fluoro-2-deoxy-D-glucose ((18)F-FDG) is extensively applied in clinical practice. However, in animal experiments, the application of clinical PET is difficult, due to limitations in sensitivity and spatial resolution. This study aimed to determine the potential of (18)F-FDG PET with regard to the imaging of human laryngeal squamous cell carcinoma (LSCC) xenografts. Twenty-seven LSCC tumor-bearing nude mice were divided randomly into seven groups which were each handled differently; the anesthetization, fasting, warming and the time point at which scanning was initiated were varied. The size of each xenograft was measured prior to conducting the scan. Using the RAMLA 3D image reconstruction method, images were acquired. The region of interest (ROI) technology was adopted to calculate target and non-target (T/N) ratios. The results were subsequently analyzed by semiquantitative analysis. The analysis showed that there was no significant correlation between tumor size and PET image quality (r=0.381, P>0.05); however, the handling conditions of the mice had a greater influence on the tumor image quality. Fasting increased (18)F-FDG uptake (T/N, 1.153±0.008) to a certain degree, although the effect was unstable. By contrast, combining warming and fasting increased (18)F-FDG uptake significantly (T/N, 2.0±0.29; P<0.05). The acquisition time had no impact on the tumor image quality. The study demonstrated that the application of clinical PET scanning has potential in the study of human LSCC xenografts in nude mice, and that the quality of the image of the tumor is greatly influenced by the handling conditions of the animals.
format Online
Article
Text
id pubmed-3786834
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-37868342013-10-17 Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts XU, OU LI, XIAOMING SHAN, CHUNGUANG YANG, XING ZHANG, LIN WANG, JINGMIAO Exp Ther Med Articles Positron emission tomography (PET) imaging with [F-18]-fluoro-2-deoxy-D-glucose ((18)F-FDG) is extensively applied in clinical practice. However, in animal experiments, the application of clinical PET is difficult, due to limitations in sensitivity and spatial resolution. This study aimed to determine the potential of (18)F-FDG PET with regard to the imaging of human laryngeal squamous cell carcinoma (LSCC) xenografts. Twenty-seven LSCC tumor-bearing nude mice were divided randomly into seven groups which were each handled differently; the anesthetization, fasting, warming and the time point at which scanning was initiated were varied. The size of each xenograft was measured prior to conducting the scan. Using the RAMLA 3D image reconstruction method, images were acquired. The region of interest (ROI) technology was adopted to calculate target and non-target (T/N) ratios. The results were subsequently analyzed by semiquantitative analysis. The analysis showed that there was no significant correlation between tumor size and PET image quality (r=0.381, P>0.05); however, the handling conditions of the mice had a greater influence on the tumor image quality. Fasting increased (18)F-FDG uptake (T/N, 1.153±0.008) to a certain degree, although the effect was unstable. By contrast, combining warming and fasting increased (18)F-FDG uptake significantly (T/N, 2.0±0.29; P<0.05). The acquisition time had no impact on the tumor image quality. The study demonstrated that the application of clinical PET scanning has potential in the study of human LSCC xenografts in nude mice, and that the quality of the image of the tumor is greatly influenced by the handling conditions of the animals. D.A. Spandidos 2013-09 2013-07-03 /pmc/articles/PMC3786834/ /pubmed/24137257 http://dx.doi.org/10.3892/etm.2013.1200 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
XU, OU
LI, XIAOMING
SHAN, CHUNGUANG
YANG, XING
ZHANG, LIN
WANG, JINGMIAO
Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts
title Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts
title_full Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts
title_fullStr Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts
title_full_unstemmed Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts
title_short Application of clinical PET imaging to human laryngeal squamous cell carcinoma xenografts
title_sort application of clinical pet imaging to human laryngeal squamous cell carcinoma xenografts
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786834/
https://www.ncbi.nlm.nih.gov/pubmed/24137257
http://dx.doi.org/10.3892/etm.2013.1200
work_keys_str_mv AT xuou applicationofclinicalpetimagingtohumanlaryngealsquamouscellcarcinomaxenografts
AT lixiaoming applicationofclinicalpetimagingtohumanlaryngealsquamouscellcarcinomaxenografts
AT shanchunguang applicationofclinicalpetimagingtohumanlaryngealsquamouscellcarcinomaxenografts
AT yangxing applicationofclinicalpetimagingtohumanlaryngealsquamouscellcarcinomaxenografts
AT zhanglin applicationofclinicalpetimagingtohumanlaryngealsquamouscellcarcinomaxenografts
AT wangjingmiao applicationofclinicalpetimagingtohumanlaryngealsquamouscellcarcinomaxenografts