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In vivo 18F‑fluorodeoxyglucose‑positron emission tomography/computed tomography imaging of pancreatic tumors in a transgenic rat model carrying the human KRASG12V oncogene
https://repo.qst.go.jp/records/47133
https://repo.qst.go.jp/records/47133c95aea76-4aa8-4011-97c6-d4a43b9a13b2
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2015-05-11 | |||||
タイトル | ||||||
タイトル | In vivo 18F‑fluorodeoxyglucose‑positron emission tomography/computed tomography imaging of pancreatic tumors in a transgenic rat model carrying the human KRASG12V oncogene | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Shibata, Koji
× Shibata, Koji× Fukamachi, Katsumi× Tsuji, Atsushi× Saga, Tsuneo× Futakuchi, Mitsuru× Nagino, Masato× Tsuda, Hiroyuki× Suzuki, Masumi× 辻 厚至× 佐賀 恒夫 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | A novel KRAS‑mediated transgenic rat model has previously been demonstrated, in which animals develop multiple pancreatic ductal adenocarcinoma (PDAC) that is histologically similar to human PDAC within two weeks. Positron emission tomography (PET)/computed tomography (CT) is commonly used for the diagnosis and staging of PDAC in humans, and can be adopted for optimal use in animal experiments. The aim of the present study was to evaluate the carcinogenic process in a rat pancreatic carcinoma model using small‑animal multimodality imaging systems. The utility of fluorodeoxyglucose (FDG)‑PET/CT in detecting the location and size of PDAC during tumor development in the present transgenic rat model was assessed. A small animal multimodality PET/CT system and contrast‑enhanced CT (CECT) system were used for the imaging analysis of KRASG12V male transgenic rats (n=6), which developed pancreatic tumors following the administration of an injection of Cre recombinase (Cre)‑carrying adenovirus. Laparotomies performed at six weeks post‑treatment revealed that all three (100%) Cre‑expressing rats developed pancreatic tumors that were <2 mm in diameter, none of which were detected by 18F‑FDG PET/CT or CECT. At eight weeks post‑treatment, the pancreatic tumors were heterogeneously visualized by 18F‑FDG‑PET/CT and CECT in two of the three rats. Furthermore, the autopsies confirmed that all three rats had developed pancreatic tumors. These novel findings provide evidence that the FDG‑PET/CT imaging system is a valuable tool for the evaluation of the carcinogenic process, and one which may aid in treatment and preventive methods for pancreatic tumors in mammalian models. A limitation associated with the early detection of PDACs warrants further investigation. | |||||
書誌情報 |
Oncology Letters 巻 9, 号 5, p. 2112-2118, 発行日 2015-03 |
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出版者 | ||||||
出版者 | Spandidos Publications | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1792-1074 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.3892/ol.2015.3053 |