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Comparison of Conventional and Novel PET Tracers for Imaging Mesothelioma in Nude Mice with Subcutaneous and Intrapleural Xenografts
https://repo.qst.go.jp/records/45528
https://repo.qst.go.jp/records/45528a2f311af-09dc-4279-8022-9e4d8bdeca16
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2009-06-09 | |||||
タイトル | ||||||
タイトル | Comparison of Conventional and Novel PET Tracers for Imaging Mesothelioma in Nude Mice with Subcutaneous and Intrapleural Xenografts | |||||
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 |
Tsuji, Atsushi
× Tsuji, Atsushi× Sogawa, Chizuru× Sugyou, Aya× Sudou, Hitomi× Koizumi, Mitsuru× Hino, Okio× Harada, Yoshinobu× Furukawa, Takako× Suzuki, Kazutoshi× Saga, Tsuneo× et.al× 辻 厚至× 曽川 千鶴× 須尭 綾× 須藤 仁美× 小泉 満× 原田 良信× 古川 高子× 鈴木 和年× 佐賀 恒夫 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Introduction Malignant mesothelioma is a highly aggressive tumor originating in the pleura, peritoneum and pericardium, and the prognosis of patients undergoing current treatment remains poor. To develop new therapies, it is important to have a noninvasive imaging system for evaluating the efficacy of such prospective treatments. We have established clinically relevant mouse models and evaluated conventional and novel positron emission tomography (PET) tracers. \nMethods Epithelioid and sarcomatoid mesothelioma cells were inoculated subcutaneously and intrapleurally into nude mice. Biodistribution and PET imaging studies were conducted by injecting [18F]fluoro-2-deoxy-d-glucose (FDG), 3'-[18F]fluoro-3'-doxythymidine (FLT) or 4'-methyl-[11C]thiothymidine (S-dThd) into the mouse models. In vitro cellular uptake of [14C]FDG and [3H]FLT and thymidine kinase 1 (TK1) activity in both cell lines were measured. Expression of glucose transporter 1 (GLUT-1) and Ki-67 in xenografted tumors was evaluated by immunohistochemical staining. \nResults In epithelioid mesothelioma models, biodistribution experiments showed that tumor uptake of [11C]S-dThd was significantly higher than that of [18F]FDG. On the other hand, in sarcomatoid models, [18F]FDG showed significantly higher accumulation than the other two tracers. These differential uptakes of the three tracers were confirmed by PET imaging. The cellular uptake of [14C]FDG and [3H]FLT and TK1 activity in sarcomatoid cells were higher than those of epithelioid cells. GLUT-1 protein was strongly expressed in sarcomatoid but not in epithelioid tumor. We observed a high percentage of Ki-67-positive cells in both epithelioid and sarcomatoid tumors. \nConclusions We established nude mouse models of epithelioid and sarcomatoid subtypes of mesothelioma. PET tracers applicable for the evaluation of epithelioid and sarcomatoid mesothelioma would vary: [18F]FLT and [11C]S-dThd seemed suitable for the epithelioid subtype and [18F]FDG seemed suitable for the sarcomatoid subtype in our mouse models. Our results indicated that cellular uptake and TK1 activity in vitro are not always consistent with tracer uptake of [18F]FLT and [11C]S-dThd in vivo. These mouse models and PET imaging might be useful tools for evaluating new and effective treatments in mesothelioma. |
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書誌情報 |
Nuclear Medicine and Biology 巻 36, 号 4, p. 379-388, 発行日 2009-03 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 0969-8051 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1016/j.nucmedbio.2009.01.018 |