Jing Zhao, Zhanwen Zhang, Dahong Nie, Hui Ma, Gongjun Yuan, Shu Su, Shaoyu Liu, Sheng Liu, Ganghua Tang
{"title":"肝细胞癌的PET成像:18f -氟丙酸作为18f -氟脱氧葡萄糖的补充放射性示踪剂","authors":"Jing Zhao, Zhanwen Zhang, Dahong Nie, Hui Ma, Gongjun Yuan, Shu Su, Shaoyu Liu, Sheng Liu, Ganghua Tang","doi":"10.1177/1536012118821032","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To evaluate the preclinical value of <sup>18</sup>F-fluoropropionic acid (<sup>18</sup>F-FPA) and <sup>18</sup>F-fluorodeoxyglucose (<sup>18</sup>F-FDG) positron emission tomography (PET) for imaging HCCs.</p><p><strong>Methods: </strong>The <sup>18</sup>F-FPA and <sup>18</sup>F-FDG uptake patterns in 3 HCC cell lines (Hep3B, HepG2, and SK-Hep1) were assessed in vitro and in vivo. The <sup>18</sup>F-FPA uptake mechanism was investigated using inhibition experiments with orlistat and 5-tetradecyloxy-2-furoic acid. The <sup>18</sup>F-FPA PET imaging was performed in different tumor animal models and compared with <sup>18</sup>F-FDG. We also evaluated the expressions of glucose transporter-1 (GLUT1), fatty acid synthase (FASN), and matrix metalloproteinase-2 (MMP2) in these cell lines.</p><p><strong>Results: </strong>In vitro experiments showed that the radiotracer uptake patterns were complementary in the HCC cell lines. Orlistat and 5-tetradecyloxy-2-furoic acid decreased the uptake of <sup>18</sup>F-FPA. The tumor-to-liver ratio of <sup>18</sup>F-FPA was superior to that of <sup>18</sup>F-FDG in the SK-Hep1 and HepG2 tumors ( P < .05). However, in the Hep3B tumors, the tumor-to-liver normalized uptake of <sup>18</sup>F-FDG was higher than <sup>18</sup>F-FPA ( P < .01). FASN was highly expressed in cell lines with high <sup>18</sup>F-FPA uptake, whereas GLUT1 was highly expressed in cell lines with high <sup>18</sup>F-FDG uptake. The <sup>18</sup>F-FPA uptake correlated with FASN ( r = 0.89, P = .014) and MMP2 ( r = 0.77, P = .002) expressions.</p><p><strong>Conclusions: </strong>PET imaging with <sup>18</sup>F-FPA combined with <sup>18</sup>F-FDG can be an alternative for detecting HCC.</p>","PeriodicalId":18855,"journal":{"name":"Molecular Imaging","volume":null,"pages":null},"PeriodicalIF":2.2000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/1536012118821032","citationCount":"7","resultStr":"{\"title\":\"PET Imaging of Hepatocellular Carcinomas: <sup>18</sup>F-Fluoropropionic Acid as a Complementary Radiotracer for <sup>18</sup>F-Fluorodeoxyglucose.\",\"authors\":\"Jing Zhao, Zhanwen Zhang, Dahong Nie, Hui Ma, Gongjun Yuan, Shu Su, Shaoyu Liu, Sheng Liu, Ganghua Tang\",\"doi\":\"10.1177/1536012118821032\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To evaluate the preclinical value of <sup>18</sup>F-fluoropropionic acid (<sup>18</sup>F-FPA) and <sup>18</sup>F-fluorodeoxyglucose (<sup>18</sup>F-FDG) positron emission tomography (PET) for imaging HCCs.</p><p><strong>Methods: </strong>The <sup>18</sup>F-FPA and <sup>18</sup>F-FDG uptake patterns in 3 HCC cell lines (Hep3B, HepG2, and SK-Hep1) were assessed in vitro and in vivo. The <sup>18</sup>F-FPA uptake mechanism was investigated using inhibition experiments with orlistat and 5-tetradecyloxy-2-furoic acid. The <sup>18</sup>F-FPA PET imaging was performed in different tumor animal models and compared with <sup>18</sup>F-FDG. We also evaluated the expressions of glucose transporter-1 (GLUT1), fatty acid synthase (FASN), and matrix metalloproteinase-2 (MMP2) in these cell lines.</p><p><strong>Results: </strong>In vitro experiments showed that the radiotracer uptake patterns were complementary in the HCC cell lines. Orlistat and 5-tetradecyloxy-2-furoic acid decreased the uptake of <sup>18</sup>F-FPA. The tumor-to-liver ratio of <sup>18</sup>F-FPA was superior to that of <sup>18</sup>F-FDG in the SK-Hep1 and HepG2 tumors ( P < .05). However, in the Hep3B tumors, the tumor-to-liver normalized uptake of <sup>18</sup>F-FDG was higher than <sup>18</sup>F-FPA ( P < .01). FASN was highly expressed in cell lines with high <sup>18</sup>F-FPA uptake, whereas GLUT1 was highly expressed in cell lines with high <sup>18</sup>F-FDG uptake. The <sup>18</sup>F-FPA uptake correlated with FASN ( r = 0.89, P = .014) and MMP2 ( r = 0.77, P = .002) expressions.</p><p><strong>Conclusions: </strong>PET imaging with <sup>18</sup>F-FPA combined with <sup>18</sup>F-FDG can be an alternative for detecting HCC.</p>\",\"PeriodicalId\":18855,\"journal\":{\"name\":\"Molecular Imaging\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2019-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1177/1536012118821032\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Imaging\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/1536012118821032\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Imaging","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/1536012118821032","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
PET Imaging of Hepatocellular Carcinomas: 18F-Fluoropropionic Acid as a Complementary Radiotracer for 18F-Fluorodeoxyglucose.
Objective: To evaluate the preclinical value of 18F-fluoropropionic acid (18F-FPA) and 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET) for imaging HCCs.
Methods: The 18F-FPA and 18F-FDG uptake patterns in 3 HCC cell lines (Hep3B, HepG2, and SK-Hep1) were assessed in vitro and in vivo. The 18F-FPA uptake mechanism was investigated using inhibition experiments with orlistat and 5-tetradecyloxy-2-furoic acid. The 18F-FPA PET imaging was performed in different tumor animal models and compared with 18F-FDG. We also evaluated the expressions of glucose transporter-1 (GLUT1), fatty acid synthase (FASN), and matrix metalloproteinase-2 (MMP2) in these cell lines.
Results: In vitro experiments showed that the radiotracer uptake patterns were complementary in the HCC cell lines. Orlistat and 5-tetradecyloxy-2-furoic acid decreased the uptake of 18F-FPA. The tumor-to-liver ratio of 18F-FPA was superior to that of 18F-FDG in the SK-Hep1 and HepG2 tumors ( P < .05). However, in the Hep3B tumors, the tumor-to-liver normalized uptake of 18F-FDG was higher than 18F-FPA ( P < .01). FASN was highly expressed in cell lines with high 18F-FPA uptake, whereas GLUT1 was highly expressed in cell lines with high 18F-FDG uptake. The 18F-FPA uptake correlated with FASN ( r = 0.89, P = .014) and MMP2 ( r = 0.77, P = .002) expressions.
Conclusions: PET imaging with 18F-FPA combined with 18F-FDG can be an alternative for detecting HCC.
Molecular ImagingBiochemistry, Genetics and Molecular Biology-Biotechnology
自引率
3.60%
发文量
21
期刊介绍:
Molecular Imaging is a peer-reviewed, open access journal highlighting the breadth of molecular imaging research from basic science to preclinical studies to human applications. This serves both the scientific and clinical communities by disseminating novel results and concepts relevant to the biological study of normal and disease processes in both basic and translational studies ranging from mice to humans.