Suppr超能文献

非活性/活性维生素D类似物与酮康唑对甲状旁腺细胞的增强作用。

Potentiating effects of nonactive/active vitamin D analogues and ketoconazole in parathyroid cells.

作者信息

Segersten Ulrika, Björklund Peyman, Hellman Per, Akerström Göran, Westin Gunnar

机构信息

Department of Surgical Sciences, Endocrine Unit, Uppsala University Hospital, Sweden.

出版信息

Clin Endocrinol (Oxf). 2007 Mar;66(3):399-404. doi: 10.1111/j.1365-2265.2006.02746.x.

Abstract

BACKGROUND AND OBJECTIVE

1,25-dihydroxyvitamin D(3)[1alpha,25(OH)(2)D(3), calcitriol], and its less calcaemic synthetic analogues have therapeutic potential in several diseases, including hyperparathyroidism (HPT). We have suggested that non-1alpha-hydroxylated (nonactive) vitamin D analogues may present an alternative in tumour cells expressing 25-hydroxyvitamin D(3) 1alpha-hydroxylase (1alpha-hydroxylase). The aim of this study was to investigate biological effects of a non-1alpha-hydroxylated vitamin D analogue in normal and tumour parathyroid cells.

PATIENTS AND METHODS

Effects of vitamin D analogues and ketoconazole on parathyroid hormone (PTH) secretion (radioimmunoassay) and PTH mRNA expression (reverse transcription-polymerase chain reaction) were studied in primary bovine parathyroid cells. Proliferation of tumour cells isolated from HPT patients was determined by thymidine incorporation.

RESULTS

EB1285, non-1alpha-hydroxylated precursor of the vitamin D analogue EB1089, suppressed PTH secretion and PTH mRNA level as well as increased expression of 25-hydroxyvitamin D(3)-24-hydroxylase (24-hydroxylase) in bovine parathyroid cells. EB1285 also inhibited cell proliferation of parathyroid tumour cells from primary (pHPT) and secondary HPT (sHPT) patients. Combined treatment with the cytochrome P450-dependent enzyme inhibitor ketoconazole and EB1285 or with active vitamin D compounds potentiated the suppressive effect on PTH secretion from bovine parathyroid cells. Ketaconazole alone displayed PTH suppression and increased 24-hydroxylase expression.

CONCLUSION

The results support the idea that a non-1alpha-hydroxylated vitamin D analogue may elicit vitamin D receptor (VDR) effects in 1alpha-hydroxylase expressing parathyroid tumour cells. Further studies are warranted to elucidate whether precursor vitamin D analogues as well as inhibitors of 24-hydroxylase present therapeutic alternatives in patients suffering from HPT.

摘要

背景与目的

1,25 - 二羟基维生素D(3)[1α,25(OH)(2)D(3),骨化三醇]及其钙血症较轻的合成类似物在包括甲状旁腺功能亢进症(HPT)在内的多种疾病中具有治疗潜力。我们曾提出,非1α - 羟基化(无活性)的维生素D类似物可能为表达25 - 羟基维生素D(3) 1α - 羟化酶(1α - 羟化酶)的肿瘤细胞提供一种替代选择。本研究的目的是探讨一种非1α - 羟基化维生素D类似物对正常及肿瘤甲状旁腺细胞的生物学效应。

患者与方法

在原代牛甲状旁腺细胞中,研究了维生素D类似物和酮康唑对甲状旁腺激素(PTH)分泌(放射免疫测定法)及PTH mRNA表达(逆转录 - 聚合酶链反应)的影响。通过胸腺嘧啶核苷掺入法测定从HPT患者分离的肿瘤细胞的增殖情况。

结果

维生素D类似物EB1089的非1α - 羟基化前体EB1285抑制了牛甲状旁腺细胞中的PTH分泌和PTH mRNA水平,并增加了25 - 羟基维生素D(3)-24 - 羟化酶(24 - 羟化酶)的表达。EB1285还抑制了原发性(pHPT)和继发性HPT(sHPT)患者甲状旁腺肿瘤细胞的增殖。细胞色素P450依赖性酶抑制剂酮康唑与EB1285联合治疗,或与活性维生素D化合物联合治疗,增强了对牛甲状旁腺细胞PTH分泌的抑制作用。单独使用酮康唑可抑制PTH分泌并增加24 - 羟化酶的表达。

结论

结果支持这样一种观点,即非1α - 羟基化维生素D类似物可能在表达1α - 羟化酶的甲状旁腺肿瘤细胞中引发维生素D受体(VDR)效应。有必要进一步研究以阐明前体维生素D类似物以及24 - 羟化酶抑制剂是否为HPT患者提供治疗选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验