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去势抵抗性前列腺癌细胞对1α-羟基维生素D5(一种骨化三醇类似物)反应中雄激素受体对维生素D受体的调节作用

Androgen Receptor regulation of Vitamin D receptor in response of castration-resistant prostate cancer cells to 1α-Hydroxyvitamin D5 - a calcitriol analog.

作者信息

Mooso Benjamin, Madhav Anisha, Johnson Sherra, Roy Mohana, Moore Mary E, Moy Christabel, Loredo Grace A, Mehta Rajendra G, Vaughan Andrew T M, Ghosh Paramita M

机构信息

VA Northern California Health Care System, Mather, CA.

出版信息

Genes Cancer. 2010 Nov 16;1(9):927-940. doi: 10.1177/1947601910385450.

Abstract

Calcitriol (1,25(OH)(2)D3) is cytostatic for prostate cancer (CaP), but had limited therapeutic utility due to hypercalcemia-related toxicities, leading to the development of low-calcemic calcitriol analogs. We show that one analog, 1-α-Hydroxyvitamin-D5 (1α(OH)D5), induced apoptosis in castration-sensitive LNCaP prostate cancer cells, but unlike calcitriol, did not increase androgen receptor (AR) transcriptional activity. LNCaP-AI, a castrate-resistant (CRCaP) LNCaP subline, was resistant to 1α(OH)D5 in the presence of androgens; however, androgen withdrawal (AWD), although ineffective by itself, sensitized LNCaP-AI cells to 1α(OH)D5. Investigation of the mechanism revealed that the vitamin D receptor (VDR), which mediates the effects of 1α(OH)D5, is downregulated in LNCaP-AI cells compared to LNCaP in the presence of androgens, whereas AWD restored VDR expression. Since LNCaP-AI cells expressed higher AR compared to LNCaP and AWD decreased AR, this indicated an inverse relationship between VDR and AR. Further, AR stimulation (by increased androgen) suppressed VDR, while AR downregulation (by ARsiRNA) stimulated VDR levels and sensitized LNCaP-AI cells to 1α(OH)D5 similar to AWD. Another cell line, pRNS-1-1, although isolated from a normal prostate, had lost AR expression in culture and adapted to androgen-independent growth. These cells expressed the VDR and were sensitive to 1α(OH)D5, but restoration of AR expression suppressed VDR levels and induced resistance to 1α(OH)D5 treatment. Taken together, these results demonstrate negative regulation of VDR by AR in CRCaP cells. This effect is likely mediated by prohibitin (PHB), which was inhibited by AR transcriptional activity and stimulated VDR in CRCaP, but not castrate-sensitive cells. Therefore, in castration sensitive cells, although the AR negatively regulates PHB, this does not affect VDR expression, whereas in CRCaP cells, negative regulation of PHB by the AR results in concomitant negative regulation of the VDR by the AR. These data demonstrate a novel mechanism by which 1α(OH)D5 prolong the effectiveness of AWD in CaP cells.

摘要

骨化三醇(1,25(OH)(2)D3)对前列腺癌(CaP)具有细胞抑制作用,但由于与高钙血症相关的毒性,其治疗效用有限,这促使了低钙血症骨化三醇类似物的研发。我们发现,一种类似物1-α-羟基维生素D5(1α(OH)D5)可诱导去势敏感的LNCaP前列腺癌细胞凋亡,但与骨化三醇不同的是,它不会增加雄激素受体(AR)的转录活性。LNCaP-AI是一种去势抵抗性(CRCaP)LNCaP亚系,在雄激素存在的情况下对1α(OH)D5具有抗性;然而,雄激素撤除(AWD)虽然自身无效,但可使LNCaP-AI细胞对1α(OH)D5敏感。机制研究表明,介导1α(OH)D5作用的维生素D受体(VDR)在雄激素存在的情况下,与LNCaP相比,在LNCaP-AI细胞中表达下调,而AWD可恢复VDR表达。由于LNCaP-AI细胞与LNCaP相比表达更高水平的AR,且AWD可降低AR水平,这表明VDR与AR之间存在负相关关系。此外,AR刺激(通过增加雄激素)可抑制VDR,而AR下调(通过ARsiRNA)可刺激VDR水平,并使LNCaP-AI细胞对1α(OH)D5敏感,类似于AWD。另一种细胞系pRNS-1-1虽然从正常前列腺中分离得到,但在培养过程中失去了AR表达,并适应了雄激素非依赖性生长。这些细胞表达VDR,对1α(OH)D5敏感,但AR表达的恢复会抑制VDR水平,并诱导对1α(OH)D5治疗的抗性。综上所述,这些结果表明在CRCaP细胞中AR对VDR具有负调控作用。这种效应可能由抑制素(PHB)介导,在CRCaP细胞中,AR转录活性可抑制PHB并刺激VDR,但在去势敏感细胞中则不然。因此,在去势敏感细胞中,虽然AR对PHB具有负调控作用,但这并不影响VDR表达,而在CRCaP细胞中,AR对PHB的负调控导致AR对VDR的负调控。这些数据证明了1α(OH)D5延长AWD在CaP细胞中有效性的一种新机制。

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