Zhou Xuanzhu, Zheng Wei, Nagana Gowda G A, Raftery Daniel, Donkin Shawn S, Bequette Brian, Teegarden Dorothy
Interdepartmental Nutrition Program, Purdue University, West Lafayette, IN 47906, United States.
Department of Chemistry, Purdue University, West Lafayette, IN 47906, United States.
J Steroid Biochem Mol Biol. 2016 Oct;163:147-56. doi: 10.1016/j.jsbmb.2016.04.022. Epub 2016 May 3.
Breast cancer is the second most common cancer among women in the US. The active form of vitamin D, 1,25-dihydroxyvitamin D (1,25(OH)2D), is proposed to inhibit cellular processes and to prevent breast cancer. The current studies investigated the effect of 1,25(OH)2D on glutamine metabolism during cancer progression employing Harvey-ras oncogene transformed MCF10A human breast epithelial cells (MCF10A-ras). Treatment with 1,25(OH)2D significantly reduced intracellular glutamine and glutamate levels measured by nuclear magnetic resonance (NMR) by 23±2% each. Further, 1,25(OH)2D treatment reduced glutamine and glutamate flux, determined by [U-(13)C5] glutamine tracer kinetics, into the TCA cycle by 31±0.2% and 17±0.4%, respectively. The relative levels of mRNA and protein abundance of the major glutamine transporter, solute linked carrier family 1 member A5 (SLC1A5), was significantly decreased by 1,25(OH)2D treatment in both MCF10A-ras cells and MCF10A which overexpress ErbB2 (HER-2/neu). Consistent with these results, glutamine uptake was reduced by 1,25(OH)2D treatment and the impact was eliminated with the SLC1A5 inhibitor L-γ-Glutamyl-p-nitroanilide (GPNA). A consensus sequence to the vitamin D responsive element (VDRE) was identified in silico in the SLC1A5 gene promoter, and site-directed mutagenesis analyses with reporter gene studies demonstrate a functional negative VDRE in the promoter of the SLC1A5 gene. siRNA-SLC1A5 transfection in MCF10A-ras cells significantly reduced SLC1A5 mRNA expression as well as decreased viable cell number similar to 1,25(OH)2D treatment. SLC1A5 knockdown also induced an increase in apoptotic cells in MCF10A-ras cells. These results suggest 1,25(OH)2D alters glutamine metabolism in MCF10A-ras cells by inhibiting glutamine uptake and utilization, in part through down-regulation of SLC1A5 transcript abundance. Thus, 1,25(OH)2D down-regulation of the glutamine transporter, SLC1A5, may facilitate vitamin D prevention of breast cancer.
乳腺癌是美国女性中第二常见的癌症。维生素D的活性形式,即1,25 - 二羟基维生素D(1,25(OH)2D),被认为可以抑制细胞进程并预防乳腺癌。目前的研究利用哈维 - 拉斯癌基因转化的MCF10A人乳腺上皮细胞(MCF10A - ras),研究了1,25(OH)2D在癌症进展过程中对谷氨酰胺代谢的影响。用1,25(OH)2D处理后,通过核磁共振(NMR)测量,细胞内谷氨酰胺和谷氨酸水平显著降低,各降低了23±2%。此外,通过[U-(13)C5]谷氨酰胺示踪动力学测定,1,25(OH)2D处理使进入三羧酸循环的谷氨酰胺和谷氨酸通量分别降低了31±0.2%和17±0.4%。在MCF10A - ras细胞和过表达ErbB2(HER - 2/neu)的MCF10A细胞中,主要谷氨酰胺转运体溶质连接载体家族1成员A5(SLC1A5)的mRNA和蛋白质丰度相对水平经1,25(OH)2D处理后均显著降低。与这些结果一致,1,25(OH)2D处理降低了谷氨酰胺摄取,而SLC1A5抑制剂L - γ - 谷氨酰 - 对硝基苯胺(GPNA)消除了这种影响。在SLC1A5基因启动子中通过计算机模拟鉴定出维生素D反应元件(VDRE)的共有序列,并且通过报告基因研究进行的定点诱变分析表明SLC1A5基因启动子中存在功能性负VDRE。在MCF10A - ras细胞中进行siRNA - SLC1A5转染显著降低了SLC1A5 mRNA表达,并且与1,25(OH)2D处理类似,降低了活细胞数量。SLC1A5基因敲低还诱导了MCF10A - ras细胞中凋亡细胞的增加。这些结果表明,1,25(OH)2D通过抑制谷氨酰胺摄取和利用来改变MCF10A - ras细胞中的谷氨酰胺代谢,部分是通过下调SLC1A5转录本丰度实现的。因此,1,25(OH)2D对谷氨酰胺转运体SLC1A5的下调可能有助于维生素D预防乳腺癌。