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GADD45γ:一种新的维生素 D 调控基因,可抑制前列腺癌细胞增殖。

GADD45gamma: a new vitamin D-regulated gene that is antiproliferative in prostate cancer cells.

机构信息

Department of Molecular and Cellular Pharmacology, University of Miami Miller School of Medicine, 1600 NW 10th Avenue, R-189, Room 6155 Rosenstiel Building, Miami, Florida 33136, USA.

出版信息

Endocrinology. 2010 Oct;151(10):4654-64. doi: 10.1210/en.2010-0434. Epub 2010 Aug 25.

Abstract

1,25-dihydroxyvitamin D3 [1,25-(OH)2D3] inhibits proliferation of normal and malignant prostate epithelial cells at least in part through inhibition of G1 to S phase cell cycle progression. The mechanisms of the antiproliferative effects of 1,25-(OH)2D3 have yet to be fully elucidated but are known to require the vitamin D receptor. We previously developed a 1,25-(OH)2D3-resistant derivative of the human prostate cancer cell line, LNCaP, which retains active vitamin D receptors but is not growth inhibited by 1,25-(OH)2D3. Gene expression profiling revealed two novel 1,25-(OH)2D3-inducible genes, growth arrest and DNA damage-inducible gene gamma (GADD45γ) and mitogen induced gene 6 (MIG6), in LNCaP but not in 1,25-(OH)2D3-resistant cells. GADD45γ up-regulation was associated with growth inhibition by 1,25-(OH)2D3 in human prostate cancer cells. Ectopic expression of GADD45γ in either LNCaP or ALVA31 cells resulted in G1 accumulation and inhibition of proliferation equal to or greater than that caused by 1,25-(OH)2D3 treatment. In contrast, ectopic expression of MIG6 had only minimal effects on cell cycle distribution and proliferation. Whereas GADD45γ has been shown to be induced by androgens in prostate cancer cells, up-regulation of GADD45γ by 1,25-(OH)2D3 was not dependent on androgen receptor signaling, further refuting a requirement for androgens/androgen receptor in vitamin D-mediated growth inhibition. These data introduce two novel 1,25-(OH)2D3-regulated genes and establish GADD45γ as a growth-inhibitory protein in prostate cancer. Furthermore, the induction of GADD45γ gene expression by 1,25-(OH)2D3 may mark therapeutic response in prostate cancer.

摘要

1,25-二羟维生素 D3[1,25-(OH)2D3] 通过抑制 G1 期到 S 期细胞周期进程至少部分抑制正常和恶性前列腺上皮细胞的增殖。1,25-(OH)2D3 的抗增殖作用的机制尚未完全阐明,但已知需要维生素 D 受体。我们之前开发了一种人前列腺癌细胞系 LNCaP 的 1,25-(OH)2D3 抗性衍生物,该细胞保留有活性的维生素 D 受体,但不受 1,25-(OH)2D3 的生长抑制。基因表达谱分析显示,LNCaP 中有两个新的 1,25-(OH)2D3 诱导基因,生长停滞和 DNA 损伤诱导基因γ(GADD45γ)和有丝分裂原诱导基因 6(MIG6),但在 1,25-(OH)2D3 抗性细胞中则没有。GADD45γ 的上调与 1,25-(OH)2D3 在人前列腺癌细胞中的生长抑制有关。在 LNCaP 或 ALVA31 细胞中外源表达 GADD45γ 导致 G1 期积累和增殖抑制,与 1,25-(OH)2D3 处理引起的增殖抑制相当或更大。相比之下,MIG6 的异位表达对细胞周期分布和增殖只有很小的影响。虽然 GADD45γ 已被证明在前列腺癌细胞中受到雄激素的诱导,但 1,25-(OH)2D3 对 GADD45γ 的上调不依赖于雄激素受体信号,进一步反驳了维生素 D 介导的生长抑制需要雄激素/雄激素受体。这些数据引入了两个新的 1,25-(OH)2D3 调节基因,并确立 GADD45γ 为前列腺癌中的生长抑制蛋白。此外,1,25-(OH)2D3 诱导 GADD45γ 基因表达可能标志着前列腺癌的治疗反应。

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