Xu S, Adisetiyo H, Tamura S, Grande F, Garofalo A, Roy-Burman P, Neamati N
Department of Medicinal Chemistry, College of Pharmacy, Translational Oncology Program, University of Michigan, Ann Arbor, MI 48109, USA.
Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Br J Cancer. 2015 Jul 14;113(2):242-51. doi: 10.1038/bjc.2015.228. Epub 2015 Jun 23.
Survivin and monoamine oxidase A (MAOA) levels are elevated in prostate cancer (PCa) compared to normal prostate glands. However, the relationship between survivin and MAOA in PCa is unclear.
We examined MAOA expression in the prostate lobes of a conditional PTEN-deficient mouse model mirroring human PCa, with or without survivin knockout. We also silenced one gene at a time and examined the expression of the other. We further evaluated the combination of MAOA inhibitors and survivin suppressants on the growth, viability, migration and invasion of PCa cells.
Survivin and MAOA levels are both increased in clinical PCa tissues and significantly associated with patients' survival. Survivin depletion delayed MAOA increase during PCa progression, and silencing MAOA decreased survivin expression. The combination of MAOA inhibitors and the survivin suppressants (YM155 and SC144) showed significant synergy on the inhibition of PCa cell growth, migration and invasion with concomitant decrease in survivin and MMP-9 levels.
There is a positive feedback loop between survivin and MAOA expression in PCa. Considering that survivin suppressants and MAOA inhibitors are currently available in clinical trials and clinical use, their synergistic effects in PCa support a rapid translation of this combination to clinical practice.
与正常前列腺组织相比,前列腺癌(PCa)中生存素和单胺氧化酶A(MAOA)水平升高。然而,PCa中生存素与MAOA之间的关系尚不清楚。
我们在模拟人类PCa的条件性PTEN缺陷小鼠模型的前列腺叶中检测了MAOA的表达,该模型有或没有生存素基因敲除。我们还一次沉默一个基因并检测另一个基因的表达。我们进一步评估了MAOA抑制剂和生存素抑制剂联合使用对PCa细胞生长、活力、迁移和侵袭的影响。
临床PCa组织中生存素和MAOA水平均升高,且与患者生存显著相关。在PCa进展过程中,生存素缺失延迟了MAOA的升高,而沉默MAOA则降低了生存素的表达。MAOA抑制剂与生存素抑制剂(YM155和SC144)联合使用对抑制PCa细胞生长、迁移和侵袭具有显著协同作用,同时生存素和MMP-9水平降低。
PCa中生存素与MAOA表达之间存在正反馈回路。鉴于目前生存素抑制剂和MAOA抑制剂已进入临床试验和临床应用阶段,它们在PCa中的协同作用支持将这种联合治疗迅速转化为临床实践。