Gallardo-Williams Maria T, Maronpot Robert R, Wine Robert N, Brunssen Susan H, Chapin Robert E
Laboratory of Molecular Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
Prostate. 2003 Jan 1;54(1):44-9. doi: 10.1002/pros.10166.
Prostate specific antigen (PSA) is a well-established marker of prostate cancer, but it can also degrade extracellular matrix proteins such as fibronectin and could be involved in tumor progression and metastasis. In this study, we have addressed the use of boric acid and 3-nitrophenyl boronic acid (NPBA) as PSA inhibitors in vitro.
The inhibition of PSA by boric acid was studied by using specific fluorogenic substrates. Fibronectin, a biologically relevant substrate for PSA, was used as a substrate in a zymographic assay, and the degradation of fibronectin by PSA in the presence of boric acid and NPBA was followed by Western Blot.
Low concentrations of boric acid partially inhibited the proteolytic activity of PSA toward a synthetic fluorogenic substrate. Also, by Western blot, we have found significant inhibition in the proteolysis of fibronectin by PSA in the presence of boric acid as well as NPBA. Results indicate that the boronated compounds used in this study can be used for the modulation of PSA activity.
PSA activity is inhibited in vitro by boric acid and NPBA. If degradation of fibronectin by PSA were, in fact, an important step in the progression of prostate cancer, then borate-induced inhibition of PSA activity should help reduce the development and proliferation of prostate carcinomas.
前列腺特异性抗原(PSA)是一种公认的前列腺癌标志物,但它也能降解细胞外基质蛋白,如纤连蛋白,并且可能参与肿瘤进展和转移。在本研究中,我们探讨了硼酸和3-硝基苯硼酸(NPBA)作为体外PSA抑制剂的用途。
通过使用特异性荧光底物研究硼酸对PSA的抑制作用。纤连蛋白是PSA的一种生物学相关底物,在酶谱分析中用作底物,通过蛋白质印迹法观察在硼酸和NPBA存在下PSA对纤连蛋白的降解情况。
低浓度硼酸部分抑制了PSA对合成荧光底物的蛋白水解活性。此外,通过蛋白质印迹法,我们发现在硼酸和NPBA存在下,PSA对纤连蛋白的蛋白水解有显著抑制作用。结果表明,本研究中使用的硼化合物可用于调节PSA活性。
硼酸和NPBA在体外抑制PSA活性。如果PSA对纤连蛋白的降解实际上是前列腺癌进展中的一个重要步骤,那么硼酸盐诱导的PSA活性抑制应有助于减少前列腺癌的发生和增殖。