Balanathan P, Williams E D, Wang H, Pedersen J S, Horvath L G, Achen M G, Stacker S A, Risbridger G P
Centre for Urological Research, Monash Institute of Medical Research, Monash University, Melbourne, Victoria 3168, Australia.
Br J Cancer. 2009 Jun 2;100(11):1784-93. doi: 10.1038/sj.bjc.6605089. Epub 2009 May 12.
The biological function of inhibin-alpha subunit (INH alpha) in prostate cancer (PCa) is currently unclear. A recent study associated elevated levels of INH alpha in PCa patients with a higher risk of recurrence. This prompted us to use clinical specimens and functional studies to investigate the pro-tumourigenic and pro-metastatic function of INH alpha. We conducted a cross-sectional study to determine a link between INH alpha expression and a number of clinicopathological parameters including Gleason score, surgical margin, extracapsular spread, lymph node status and vascular endothelial growth factor receptor-3 expression, which are well-established prognostic factors of PCa. In addition, using two human PCa cell lines (LNCaP and PC3) representing androgen-dependent and -independent PCa respectively, we investigated the biological function of elevated levels of INH alpha in advanced cancer. Elevated expression of INH alpha in primary PCa tissues showed a higher risk of PCa patients being positive for clinicopathological parameters outlined above. Over-expressing INH alpha in LNCaP and PC3 cells demonstrated two different and cell-type-specific responses. INH alpha-positive LNCaP demonstrated reduced tumour growth whereas INH alpha-positive PC3 cells demonstrated increased tumour growth and metastasis through the process of lymphangiogenesis. This study is the first to demonstrate a pro-tumourigenic and pro-metastatic function for INH alpha associated with androgen-independent stage of metastatic prostate disease. Our results also suggest that INH alpha expression in the primary prostate tumour can be used as a predictive factor for prognosis of PCa.
抑制素α亚基(INHα)在前列腺癌(PCa)中的生物学功能目前尚不清楚。最近的一项研究表明,PCa患者中INHα水平升高与复发风险较高有关。这促使我们利用临床标本和功能研究来探究INHα的促肿瘤发生和促转移功能。我们进行了一项横断面研究,以确定INHα表达与一些临床病理参数之间的联系,这些参数包括 Gleason评分、手术切缘、包膜外扩散、淋巴结状态和血管内皮生长因子受体-3表达,它们都是公认的PCa预后因素。此外,我们使用分别代表雄激素依赖性和非依赖性PCa的两个人类PCa细胞系(LNCaP和PC3),研究了晚期癌症中INHα水平升高的生物学功能。原发性PCa组织中INHα的高表达表明PCa患者出现上述临床病理参数阳性的风险更高。在LNCaP和PC3细胞中过表达INHα表现出两种不同的、细胞类型特异性的反应。INHα阳性的LNCaP表现出肿瘤生长减少,而INHα阳性的PC3细胞则通过淋巴管生成过程表现出肿瘤生长和转移增加。本研究首次证明了INHα在转移性前列腺疾病雄激素非依赖性阶段具有促肿瘤发生和促转移功能。我们的结果还表明,原发性前列腺肿瘤中INHα的表达可作为PCa预后的预测因子。