Tang Yong, Wang Man-Tzu, Chen Yakun, Yang Dianer, Che Mingxin, Honn Kenneth V, Akers Gregory D, Johnson Stephen R, Nie Daotai
Department of Medical Microbiology, Immunology, and Cell Biology, Southern Illinois University School of Medicine and SimmonsCooper Cancer Institute, Springfield, IL 62794-9626, USA.
Int J Cancer. 2009 Apr 1;124(7):1545-51. doi: 10.1002/ijc.24118.
The enzyme 15-lipoxygenase-2 (15-LOX-2) utilizes arachidonic acid, a polyunsaturated fatty acid, to synthesize 15(S)-hydroxyeicosatetraenoic acid. Abundantly expressed in normal prostate epithelium but frequently suppressed in the cancerous tissues, 15-LOX-2 has been suggested as a functional suppressor of prostate cancer, but the mechanism(s) involved remains unknown. To study the functional role of 15-LOX-2 in prostate cancer, we expressed 15-LOX-2 as a fusion protein with GFP in DU145 and PC-3 cells and found that 15-LOX-2 increased cell cycle arrest at G0/G1 phase. When injected into athymic nu/nu mice, prostate cancer cells with 15-LOX-2 expression could still form palpable tumors without significant changes in tumorigenicity. But, the tumors with 15-LOX-2 expression grew significantly slower than those derived from vector controls and were kept dormant for a long period of time. Histological evaluation revealed an increase in cell death in tumors derived from prostate cancer cells with 15-LOX-2 expression, while in vitro cell culture conditions, no such increase in apoptosis was observed. Further studies found that the expression of vascular endothelial growth factor A (VEGF-A) was significantly reduced in prostate cancer cells with 15-LOX-2 expression restored. Our studies suggest that 15-LOX-2 suppresses VEGF gene expression and sustains tumor dormancy in prostate cancer. Loss of 15-LOX-2 functionalities, therefore, represents a key step for prostate cancer cells to exit from dormancy and embark on malignant progression in vivo.
15-脂氧合酶-2(15-LOX-2)利用多不饱和脂肪酸花生四烯酸合成15(S)-羟基二十碳四烯酸。15-LOX-2在正常前列腺上皮中大量表达,但在癌组织中常被抑制,有人提出它是前列腺癌的功能性抑制因子,但其相关机制尚不清楚。为了研究15-LOX-2在前列腺癌中的功能作用,我们在DU145和PC-3细胞中将15-LOX-2表达为与绿色荧光蛋白(GFP)的融合蛋白,发现15-LOX-2增加了细胞在G0/G1期的周期阻滞。当将表达15-LOX-2的前列腺癌细胞注射到无胸腺裸鼠体内时,仍可形成可触及的肿瘤,且致瘤性无明显变化。但是,表达15-LOX-2的肿瘤生长明显慢于载体对照来源的肿瘤,并长时间保持休眠状态。组织学评估显示,表达15-LOX-2的前列腺癌细胞衍生的肿瘤中细胞死亡增加,而在体外细胞培养条件下,未观察到凋亡增加。进一步研究发现,恢复15-LOX-2表达的前列腺癌细胞中血管内皮生长因子A(VEGF-A)的表达显著降低。我们的研究表明,15-LOX-2抑制VEGF基因表达并维持前列腺癌的肿瘤休眠。因此,15-LOX-2功能丧失是前列腺癌细胞在体内从休眠状态转变为恶性进展的关键步骤。