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11C放射性药物在仓鼠格林黑色素瘤中的定位。

Localization of 11C-radiopharmaceuticals in the Greene melanoma of hamsters.

作者信息

Turner J H, Maziere M, Comar D

出版信息

Eur J Nucl Med. 1985;10(9-10):392-7. doi: 10.1007/BF00256577.

DOI:10.1007/BF00256577
PMID:3159576
Abstract

Seventy Syrian golden hamsters bearing SC transplants of Greene melanoma were used to evaluate the degree of tumour uptake of several 11C-radiopharmaceuticals selected for their potential specificity for melanoma. Tissue distribution studies were performed at 30 and 60 min after IV injection of 11C-compounds and compared with the 24-h uptake of 67Ga-citrate. Gamma camera images were also compared. The highest tumour uptake at 1 h was observed with 11C-methionine (2.42% +/- 0.72%) and although activity in liver, spleen and kidney exceeded that in melanoma the tumour was demonstrated on gamma camera imaging. Melanoma localisation of 11C-chlorpromazine, 11C-flunitrazepam and 11C-ketanserine was comparable at 1% of the dose injected per gram of tumour. High activity in other organs, particularly liver, exceeded uptake in melanoma and attempts at tumour imaging were unsuccessful. Tumour accumulation of 11C-methiodide quinuclidinyl benzylate (MQNB), an 11C-imidazobenzodiazepine (Ro-15-1788) and 14C-pimozide was low and imaging studies were not attempted. None of the 11C-radiopharmaceuticals evaluated for melanoma affinity matched that of 67Ga-citrate. The 24-h tumour uptake of 67Ga-citrate was 4.07% +/- 1.37% dose injected per gram which allowed delineation of the melanoma by gamma camera imaging.

摘要

选用70只皮下移植了格林黑色素瘤的叙利亚金黄地鼠,以评估几种因对黑色素瘤具有潜在特异性而挑选出的11C放射性药物的肿瘤摄取程度。在静脉注射11C化合物后30分钟和60分钟进行组织分布研究,并与67Ga枸橼酸盐的24小时摄取情况进行比较。还比较了γ相机图像。11C-蛋氨酸在1小时时肿瘤摄取最高(2.42%±0.72%),尽管肝脏、脾脏和肾脏中的活性超过黑色素瘤,但在γ相机成像中仍可显示出肿瘤。11C-氯丙嗪、11C-氟硝西泮和11C-酮色林在黑色素瘤中的定位相当,每克肿瘤摄取量为注射剂量的1%。其他器官,特别是肝脏中的高活性超过了黑色素瘤中的摄取,肿瘤成像尝试未成功。11C-甲基碘化奎宁环苄酯(MQNB)、一种11C-咪唑并苯二氮䓬(Ro-15-1788)和14C-匹莫齐特在肿瘤中的蓄积较低,未进行成像研究。所评估的用于黑色素瘤亲和力的11C放射性药物均无法与67Ga枸橼酸盐相匹配。67Ga枸橼酸盐在24小时时每克肿瘤的摄取量为注射剂量的4.07%±1.37%,这使得γ相机成像能够勾勒出黑色素瘤的轮廓。

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2
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Active melanogenesis in non-S phase melanocytes in B16 melanomas in vivo investigated by double-tracer microautoradiography with 18F-fluorodopa and 3H-thymidine.

本文引用的文献

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A spontaneous melanoma in the hamster with a propensity for amelanotic alteration and sarcomatous transformation during transplantation.一只仓鼠身上的自发性黑色素瘤,在移植过程中倾向于无黑色素改变和肉瘤样转化。
Cancer Res. 1958 May;18(4):422-5.
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Synthesis of a 11C-labelled neuroleptic drug: pimozide.一种11C标记的抗精神病药物:匹莫齐特的合成。
采用18F-氟多巴和3H-胸腺嘧啶核苷双示踪显微放射自显影技术对体内B16黑色素瘤中非S期黑色素细胞的活跃黑色素生成进行研究。
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Int J Appl Radiat Isot. 1980 Sep;31(9):545-8. doi: 10.1016/0020-708x(80)90095-2.
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Studies on the transport of tyrosine, leucine, and methionine in cultured B-16 mouse melanoma cells.关于培养的B - 16小鼠黑色素瘤细胞中酪氨酸、亮氨酸和蛋氨酸转运的研究。
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Effects of dopamine agonists and antagonists on murine melanoma: correlation with dopamine binding activity.多巴胺激动剂和拮抗剂对小鼠黑色素瘤的影响:与多巴胺结合活性的相关性。
Cancer. 1982 Mar 15;49(6):1178-84. doi: 10.1002/1097-0142(19820315)49:6<1178::aid-cncr2820490619>3.0.co;2-h.
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Narrower margins for clinical stage I malignant melanoma.临床I期恶性黑色素瘤的切缘更窄。
N Engl J Med. 1982 Feb 25;306(8):479-82. doi: 10.1056/NEJM198202253060810.
7
Chlorpromazine distribution in hamsters and mice bearing transplantable melanoma.氯丙嗪在携带可移植性黑色素瘤的仓鼠和小鼠体内的分布。
Cancer Res. 1982 Feb;42(2):556-62.
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