Katharina Marten , Frauke Alves , Tim Feuerstein , Matthias Funke , Christoph Engelke , Lutz F. Tietze , Klaus Nebendahl , Lorenz Trümper , Christiane Jakob , Eckhardt Grabbe
{"title":"原位严重联合免疫缺陷小鼠肺腺癌模型的多层螺旋计算机断层扫描","authors":"Katharina Marten , Frauke Alves , Tim Feuerstein , Matthias Funke , Christoph Engelke , Lutz F. Tietze , Klaus Nebendahl , Lorenz Trümper , Christiane Jakob , Eckhardt Grabbe","doi":"10.1016/S0939-8600(03)80001-9","DOIUrl":null,"url":null,"abstract":"<div><h3>Background and Aim:</h3><p>In recent years, much research interest has been rightfully directed towards modelling human disease. The increasing demand of laboratory animals has led to a major impetus in small animal imaging. We evaluated the feasibility of using multislice spiral CT (MSCT) technology in a severe combined immunodeficiency (SCID) mouse model for non-small cell lung cancer.</p></div><div><h3>Materials and Methods:</h3><p>Mice (n = 14) were implanted orthotopically with the human non-small cell lung adenocarcinoma cell line A 549. Mice were scanned with MSCT and sacrificed 7 days (n = 3), 14 days (n = 3), and 21 days (n = 5) after tumor cell implantation, respectively. Histopathology was performed. Tumor size as revealed by imaging and pathology was correlated. A group of animals (n = 3) received anti-cancer treatment with seco-CBI-Q-galatoside. Those mice were scanned with MSCT 21 days after tumor implantation and sacrificed, and histopathologic work-up was performed.</p></div><div><h3>Results:</h3><p>A total of 14 mice with 14 macroscopically visible and 5 microscopically appreciable adenocarcinomas of the lung were examined. All macroscopically visible tumors were readily depicted with MSCT except from 2 lesions of 1 mm in diameter. MSCT accurately displayed the different tumor sizes in treated vs. non-treated animals.</p></div><div><h3>Discussion:</h3><p>MSCT proved to be a valuable tool for imaging of a murine lung cancer model. This evidences a potential use of this technology in small animal lung cancer imaging.</p></div>","PeriodicalId":77206,"journal":{"name":"Journal of experimental animal science","volume":"42 4","pages":"Pages 181-191"},"PeriodicalIF":0.0000,"publicationDate":"2003-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0939-8600(03)80001-9","citationCount":"0","resultStr":"{\"title\":\"Multislice spiral computed tomography of an orthotopic severe combined immunodeficient mouse model for lung adenocarcinoma\",\"authors\":\"Katharina Marten , Frauke Alves , Tim Feuerstein , Matthias Funke , Christoph Engelke , Lutz F. Tietze , Klaus Nebendahl , Lorenz Trümper , Christiane Jakob , Eckhardt Grabbe\",\"doi\":\"10.1016/S0939-8600(03)80001-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background and Aim:</h3><p>In recent years, much research interest has been rightfully directed towards modelling human disease. The increasing demand of laboratory animals has led to a major impetus in small animal imaging. We evaluated the feasibility of using multislice spiral CT (MSCT) technology in a severe combined immunodeficiency (SCID) mouse model for non-small cell lung cancer.</p></div><div><h3>Materials and Methods:</h3><p>Mice (n = 14) were implanted orthotopically with the human non-small cell lung adenocarcinoma cell line A 549. Mice were scanned with MSCT and sacrificed 7 days (n = 3), 14 days (n = 3), and 21 days (n = 5) after tumor cell implantation, respectively. Histopathology was performed. Tumor size as revealed by imaging and pathology was correlated. A group of animals (n = 3) received anti-cancer treatment with seco-CBI-Q-galatoside. Those mice were scanned with MSCT 21 days after tumor implantation and sacrificed, and histopathologic work-up was performed.</p></div><div><h3>Results:</h3><p>A total of 14 mice with 14 macroscopically visible and 5 microscopically appreciable adenocarcinomas of the lung were examined. All macroscopically visible tumors were readily depicted with MSCT except from 2 lesions of 1 mm in diameter. MSCT accurately displayed the different tumor sizes in treated vs. non-treated animals.</p></div><div><h3>Discussion:</h3><p>MSCT proved to be a valuable tool for imaging of a murine lung cancer model. This evidences a potential use of this technology in small animal lung cancer imaging.</p></div>\",\"PeriodicalId\":77206,\"journal\":{\"name\":\"Journal of experimental animal science\",\"volume\":\"42 4\",\"pages\":\"Pages 181-191\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0939-8600(03)80001-9\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of experimental animal science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0939860003800019\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of experimental animal science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0939860003800019","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Multislice spiral computed tomography of an orthotopic severe combined immunodeficient mouse model for lung adenocarcinoma
Background and Aim:
In recent years, much research interest has been rightfully directed towards modelling human disease. The increasing demand of laboratory animals has led to a major impetus in small animal imaging. We evaluated the feasibility of using multislice spiral CT (MSCT) technology in a severe combined immunodeficiency (SCID) mouse model for non-small cell lung cancer.
Materials and Methods:
Mice (n = 14) were implanted orthotopically with the human non-small cell lung adenocarcinoma cell line A 549. Mice were scanned with MSCT and sacrificed 7 days (n = 3), 14 days (n = 3), and 21 days (n = 5) after tumor cell implantation, respectively. Histopathology was performed. Tumor size as revealed by imaging and pathology was correlated. A group of animals (n = 3) received anti-cancer treatment with seco-CBI-Q-galatoside. Those mice were scanned with MSCT 21 days after tumor implantation and sacrificed, and histopathologic work-up was performed.
Results:
A total of 14 mice with 14 macroscopically visible and 5 microscopically appreciable adenocarcinomas of the lung were examined. All macroscopically visible tumors were readily depicted with MSCT except from 2 lesions of 1 mm in diameter. MSCT accurately displayed the different tumor sizes in treated vs. non-treated animals.
Discussion:
MSCT proved to be a valuable tool for imaging of a murine lung cancer model. This evidences a potential use of this technology in small animal lung cancer imaging.