Segersten Ulrika, Björklund Peyman, Hellman Per, Akerström Göran, Westin Gunnar
Department of Surgical Sciences, Endocrine Unit, Uppsala University Hospital, Sweden.
Clin Endocrinol (Oxf). 2007 Mar;66(3):399-404. doi: 10.1111/j.1365-2265.2006.02746.x.
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.
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.
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.
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.
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。
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。
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。