Sowalsky Adam G, Sager Rebecca, Schaefer Rachel J, Bratslavsky Gennady, Pandolfi Pier Paolo, Balk Steven P, Kotula Leszek
Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA.
Cancer Research Institute, Beth Israel Deaconess Cancer Center, Harvard Medical School, Boston, MA 02215, USA.
Oncotarget. 2015 May 20;6(14):12383-91. doi: 10.18632/oncotarget.3564.
Genetic alterations involving TMPRSS2-ERG alterations and deletion of key tumor suppressor genes are associated with development and progression of prostate cancer (PCa). However, less defined are early events that may contribute to the development of high-risk metastatic prostate cancer. Bioinformatic analysis of existing tumor genomic data from PCa patients revealed that WAVE complex gene alterations are associated with a greater likelihood of prostate cancer recurrence. Further analysis of primary vs. castration resistant prostate cancer indicate that disruption of WAVE complex gene expression, and particularly WAVE1 gene (WASF1) loss, is also associated with castration resistance, where WASF1 is frequently co-deleted with PTEN and resists androgen deprivation therapy (ADT). Hence, we propose that WASF1 status defines a subtype of ADT-resistant patients. Better understanding of the effects of WAVE pathway disruption will lead to development of better diagnostic and treatment modalities.
涉及TMPRSS2-ERG改变以及关键肿瘤抑制基因缺失的基因改变与前列腺癌(PCa)的发生和进展相关。然而,对于可能导致高危转移性前列腺癌发生的早期事件,人们了解较少。对来自PCa患者的现有肿瘤基因组数据进行生物信息学分析发现,WAVE复合体基因改变与前列腺癌复发的可能性更大相关。对原发性与去势抵抗性前列腺癌的进一步分析表明,WAVE复合体基因表达的破坏,尤其是WAVE1基因(WASF1)缺失,也与去势抵抗相关,其中WASF1经常与PTEN共同缺失并抵抗雄激素剥夺治疗(ADT)。因此,我们提出WASF1状态定义了一类去势抵抗患者亚型。更好地了解WAVE通路破坏的影响将有助于开发更好的诊断和治疗方法。