Gann P H, Klein K G, Chatterton R T, Ellman A E, Grayhack J T, Nadler R B, Lee C
Department of Preventive Medicine and Robert H. Lurie Cancer Center, Northwestern University Medical School, Chicago, Illinois, USA.
Prostate. 1999 Sep 1;40(4):248-55. doi: 10.1002/(sici)1097-0045(19990901)40:4<248::aid-pros6>3.0.co;2-m.
Although growth factors such as epidermal growth factor (EGF), transforming growth factor (TGF)-alpha, and TGF-beta are important regulators of prostate cell growth in vitro and in animal models, evidence to support their role in human prostate cancer development remains sparse. We previously showed that men without prostate cancer have concentrations of EGF and TGF-alpha in expressed prostatic fluid (EPF) that are individually distinct and stable over time. This study addressed whether growth factor levels in EPF are associated with the presence or progression of prostate cancer.
We measured levels of immunoreactive EGF, TGF-alpha, and TGF-beta1 in stored EPF samples from three age-matched groups: 19 men with untreated, histologically diagnosed prostate cancer (CaP), 38 with benign prostate hyperplasia (BPH), and 19 with normal prostate glands (NPD).
Median TGF-alpha was lower in the BPH group (0.45 ng/ml) than in either CaP (0.63 ng/ml) or NPD (0.58 ng/ml) groups (P = 0.03 and 0.12, respectively). For EGF, the median was lowest in the CaP group and highest in the NPD group (92.5 ng/ml vs. 175.5 ng/ml, P = 0.006). For TGF-beta1, the median level in CaP was 2.7 times higher than the median level among all controls (6.65 ng/ml vs. 2.46 ng/ml, P = 0.002). Growth factor levels were not associated with tumor stage or Gleason score. However, the single case with distant metastases had TGF-beta1 levels 23-fold higher than the CaP median.
The results suggest that at the time of CaP diagnosis, EGF levels in EPF are significantly lower, and TGF-beta1 levels significantly higher, than normal. Marked overexpression of TGF-beta1 in advanced CaP might be reflected in extremely high EPF levels.
尽管诸如表皮生长因子(EGF)、转化生长因子(TGF)-α和TGF-β等生长因子在体外和动物模型中是前列腺细胞生长的重要调节因子,但支持它们在人类前列腺癌发生中作用的证据仍然稀少。我们之前表明,没有前列腺癌的男性前列腺液(EPF)中EGF和TGF-α的浓度各自独特且随时间稳定。本研究探讨了EPF中的生长因子水平是否与前列腺癌的存在或进展相关。
我们测量了来自三个年龄匹配组的储存EPF样本中免疫反应性EGF、TGF-α和TGF-β1的水平:19名未经治疗、经组织学诊断为前列腺癌(CaP)的男性,38名患有良性前列腺增生(BPH)的男性,以及19名前列腺正常(NPD)的男性。
BPH组中TGF-α的中位数(0.45 ng/ml)低于CaP组(0.63 ng/ml)和NPD组(0.58 ng/ml)(P分别为0.03和0.12)。对于EGF,中位数在CaP组中最低,在NPD组中最高(92.5 ng/ml对175.5 ng/ml,P = 0.006)。对于TGF-β1,CaP组的中位数水平比所有对照组的中位数水平高2.7倍(6.65 ng/ml对2.46 ng/ml,P = 0.002)。生长因子水平与肿瘤分期或Gleason评分无关。然而,有远处转移的单个病例的TGF-β1水平比CaP组中位数高23倍。
结果表明,在CaP诊断时,EPF中的EGF水平显著低于正常水平,而TGF-β1水平显著高于正常水平。晚期CaP中TGF-β1的明显过表达可能反映在EPF水平极高。