Investigation of tumor metastatic potential with N-[18F]fluoroacetyl-d-glucosamine

Kazuo Kubota , Kiichi Ishiwata , Masao Tada , Susumu Yamada , Roko Kubota , Ren Iwata , Kazunori Sato , Koji Kimata , Tatsuo Ido
{"title":"Investigation of tumor metastatic potential with N-[18F]fluoroacetyl-d-glucosamine","authors":"Kazuo Kubota ,&nbsp;Kiichi Ishiwata ,&nbsp;Masao Tada ,&nbsp;Susumu Yamada ,&nbsp;Roko Kubota ,&nbsp;Ren Iwata ,&nbsp;Kazunori Sato ,&nbsp;Koji Kimata ,&nbsp;Tatsuo Ido","doi":"10.1016/0883-2897(92)90135-L","DOIUrl":null,"url":null,"abstract":"<div><p>In order to investigate the metastatic potential of tumors <em>in vivo</em> by measuring hyaluronic acid metabolism, C57BL/6 mice with B16 melanoma variants and C3H/He mice with FM3A tumor variants were evaluated using <em>N</em>-[<sup>18</sup>F]fluoroacetyl-<span>d</span>-glucosamine (<sup>18</sup>F-GlcNFAc). The uptake of <sup>18</sup>F-GlcNFAc was slightly higher (<em>P</em> &lt; 0.05) in B16-F10 tumors (high metastatic potential) than in B16-F1 (low metastatic potential). Analysis of metabolites showed that acid-insoluble fraction was the largest one in the liver by 60 min, whereas in the tumors, phosphates fraction was the major metabolite. Slower metabolism in tumors was suggested, and it may be one of the reasons for the difficulty of detecting the characteristics of their hyaluronic acid synthesis. <sup>18</sup>F-GlcNFAc uptake by FM3A variants showed no significant correlation with their metastatic potential. In addition, <em>N</em>-acetyl-<span>d</span>-[l-<sup>14</sup>C]glucosamine, 2-deoxy-<span>d</span>-[l-<sup>14</sup>C]glucose and [6-<sup>3</sup>H]thymidine failed to demonstrate any difference between tumors' metastatic variants <em>in vivo</em>.</p></div>","PeriodicalId":14328,"journal":{"name":"International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology","volume":"19 7","pages":"Pages 747-752"},"PeriodicalIF":0.0000,"publicationDate":"1992-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0883-2897(92)90135-L","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/088328979290135L","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

In order to investigate the metastatic potential of tumors in vivo by measuring hyaluronic acid metabolism, C57BL/6 mice with B16 melanoma variants and C3H/He mice with FM3A tumor variants were evaluated using N-[18F]fluoroacetyl-d-glucosamine (18F-GlcNFAc). The uptake of 18F-GlcNFAc was slightly higher (P < 0.05) in B16-F10 tumors (high metastatic potential) than in B16-F1 (low metastatic potential). Analysis of metabolites showed that acid-insoluble fraction was the largest one in the liver by 60 min, whereas in the tumors, phosphates fraction was the major metabolite. Slower metabolism in tumors was suggested, and it may be one of the reasons for the difficulty of detecting the characteristics of their hyaluronic acid synthesis. 18F-GlcNFAc uptake by FM3A variants showed no significant correlation with their metastatic potential. In addition, N-acetyl-d-[l-14C]glucosamine, 2-deoxy-d-[l-14C]glucose and [6-3H]thymidine failed to demonstrate any difference between tumors' metastatic variants in vivo.

N-[18F]氟乙酰-d-氨基葡萄糖对肿瘤转移潜能的研究
为了通过测量透明质酸代谢来研究肿瘤在体内的转移潜力,我们使用N-[18F]氟乙酰基-d-葡萄糖胺(18F- glcnfac)对B16黑色素瘤变异的C57BL/6小鼠和FM3A肿瘤变异的C3H/He小鼠进行了评估。18F-GlcNFAc的摄取略高(P <B16-F10肿瘤(高转移潜能)比B16-F1肿瘤(低转移潜能)高0.05。代谢物分析显示,60 min时肝脏中酸不溶性部分最大,而肿瘤中主要代谢物为磷酸盐部分。肿瘤中代谢较慢,这可能是难以检测其透明质酸合成特征的原因之一。FM3A变异体对18F-GlcNFAc的摄取与其转移潜能无显著相关性。此外,n -乙酰-d-[l-14C]葡萄糖、2-脱氧-d-[l-14C]葡萄糖和[6-3H]胸腺嘧啶在体内肿瘤转移变异之间没有任何差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信