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7α-甲基-17α-(E-2'-[¹²⁵I]碘乙烯基)-19-去甲睾酮:一种用于检测雄激素受体的新型放射性配体。

7 alpha-Methyl-17 alpha-(E-2'-[125I]iodovinyl)-19-nortestosterone: a new radioligand for the detection of androgen receptor.

作者信息

Hoyte R M, Brown T J, MacLusky N J, Hochberg R B

机构信息

Department of Chemistry, State University of New York, Old Westbury.

出版信息

Steroids. 1993 Jan;58(1):13-23. doi: 10.1016/0039-128x(93)90012-c.

Abstract

We have synthesized two gamma-emitting, 125I-labeled steroids, E- and Z-7 alpha-methyl-17 alpha-(2'-[125I]iodovinyl)-19-nortestosterone [125I](E- and Z-MIVNT) for specific labeling of androgen receptors. [125I]E- and [125I]Z-MIVNT were synthesized stereospecifically from E- and Z-7 alpha-methyl-17 alpha-(2'-tri-n-butylstannyl-vinyl)-19-nortestosterone. The tin adducts were prepared by addition of tri-n-butyltin hydride to 7 alpha-methyl-17 alpha-ethynyl-19-nortestosterone, and after purification they were converted in high yield to the [125I]MIVNT isomers by reaction with 125I (generated in situ by oxidation of [125I]iodide with chloramine T). The 125I-labeled products were purified by high-performance liquid chromatography, and their mass determined with an ultraviolet detector (specific activity of both, approximately 2,200 Ci/mmol). In rat prostate cytosol, [125I]E-MIVNT bound with high affinity to a single class of binding sites. Nonspecific binding in the presence of 5 alpha-dihydrotestosterone was relatively low, and compared favorably with that obtained in parallel studies with [3H]methyltrienolone (R1881). The E-isomer bound prostate cytosol with at least twice the affinity of the Z-isomer; therefore, the interaction of the E-isomer with the androgen receptor as well as other steroid receptors was studied in greater detail. Complexes of the androgen receptor with [125I]E-MIVNT as well as [3H]R1881 dissociate very slowly at 4C (kdiss for both = 0.04 h-1). Displacement studies showed that the interaction of [125I]E-MIVNT with the androgen receptor is highly specific. Competition studies showed that unlabeled E-MIVNT binds poorly to other steroid receptors in rat tissue cytosols. These binding properties make [125I]E-MIVNT a promising ligand for study of the androgen receptor, and [123I]E-MIVNT a potential imaging agent for the detection of androgen-dependent tumors, such as prostate cancer.

摘要

我们合成了两种发射γ射线的、125I标记的甾体化合物,即E-和Z-7α-甲基-17α-(2'-[125I]碘代乙烯基)-19-去甲睾酮125I,用于特异性标记雄激素受体。[125I]E-和[125I]Z-MIVNT是由E-和Z-7α-甲基-17α-(2'-三正丁基锡基-乙烯基)-19-去甲睾酮立体定向合成的。通过将三正丁基氢化锡加到7α-甲基-17α-乙炔基-19-去甲睾酮上制备锡加合物,纯化后,通过与125I(由氯胺T氧化[125I]碘化物原位生成)反应,以高产率将其转化为[125I]MIVNT异构体。125I标记的产物通过高效液相色谱法纯化,并用紫外检测器测定其质量(两者的比活度约为2,200 Ci/mmol)。在大鼠前列腺胞质溶胶中,[125I]E-MIVNT与一类单一的结合位点具有高亲和力结合。在5α-二氢睾酮存在下的非特异性结合相对较低,与用[3H]甲基三烯olone(R1881)进行的平行研究中获得的结果相比具有优势。E-异构体与前列腺胞质溶胶的结合亲和力至少是Z-异构体的两倍;因此,对E-异构体与雄激素受体以及其他甾体受体的相互作用进行了更详细的研究。雄激素受体与[125I]E-MIVNT以及[3H]R1881形成的复合物在4℃下解离非常缓慢(kdiss两者均为0.04 h-1)。置换研究表明,[125I]E-MIVNT与雄激素受体的相互作用具有高度特异性。竞争研究表明,未标记的E-MIVNT与大鼠组织胞质溶胶中的其他甾体受体结合较差。这些结合特性使[125I]E-MIVNT成为研究雄激素受体的有前景的配体,而[123I]E-MIVNT成为检测雄激素依赖性肿瘤(如前列腺癌)的潜在显像剂。

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