Steiner Thomas, Junker Kerstin, Burkhardt Frank, Braunsdorf Andreas, Janitzky Volker, Schubert Joerg
Department of Urology, Friedrich-Schiller-University, Jena, Germany.
Eur Urol. 2002 Feb;41(2):167-71. doi: 10.1016/s0302-2838(01)00030-6.
Development and especially hormone refractant progression of prostate cancer are incompletely understood. Clinical studies evaluating genetic aberrations of prior therapy biopsies in correlation with progression data in patients receiving hormone therapy for prostate cancer have not been performed until now.
After DNA isolation from histological sections of primary prostate cancer biopsies, comparative genomic hybridization (CGH) was performed according to standard protocols. Primary staging, clinical course and PSA levels of the patients were assessed.
CGH was performed on 28 primary prostate cancer samples. After a mean follow-up of 36 months 11 (39%) of the patients showed progression of disease under hormonal treatment. In patients without and with progression we found the following results, respectively: losses of 6q (41/36%), 8p (41/45%), 16q (23/18%), 18q (30/9%), and gains of 8q (12/64%; P < 0.0001) and 17 (47/26%).
Gain of 8q is found predominantly in primary core biopsies of local advanced or metastasized prostate cancers. It shows in univariate analysis significant correlation with progression in hormone treated prostate cancer. This fact suggests that gain in 8q represents a marker of aggressiveness in prostate cancer.
前列腺癌的发展,尤其是激素抵抗性进展尚未完全明确。迄今为止,尚未开展临床研究评估接受前列腺癌激素治疗患者先前治疗活检的基因畸变与进展数据之间的相关性。
从原发性前列腺癌活检组织切片中分离DNA后,按照标准方案进行比较基因组杂交(CGH)。评估患者的初始分期、临床病程和前列腺特异抗原(PSA)水平。
对28例原发性前列腺癌样本进行了CGH检测。平均随访36个月后,11例(39%)患者在激素治疗期间出现疾病进展。在无进展和有进展的患者中,我们分别发现了以下结果:6q缺失(41/36%)、8p缺失(41/45%)、16q缺失(23/18%)、18q缺失(30/9%),以及8q增益(12/64%;P < 0.0001)和17增益(47/26%)。
8q增益主要见于局部晚期或转移性前列腺癌的原发性穿刺活检中。单因素分析显示,其与激素治疗的前列腺癌进展显著相关。这一事实表明,8q增益代表前列腺癌侵袭性的一个标志物。