Cheng J, Ondracek R P, Mehedint D C, Kasza K A, Xu B, Gill S, Azabdaftari G, Yao S, Morrison C D, Mohler J L, Marshall J R
1] Department of Cancer Prevention and Population Science, Roswell Park Cancer Institute, Buffalo, NY, USA [2] Department of Pathology, University at Buffalo, Buffalo, NY, USA.
Department of Cancer Prevention and Population Science, Roswell Park Cancer Institute, Buffalo, NY, USA.
Prostate Cancer Prostatic Dis. 2015 Jun;18(2):182-9. doi: 10.1038/pcan.2015.11. Epub 2015 Apr 14.
Fatty-acid synthase (FASN), selectively overexpressed in prostate cancer (PCa) cells, has been described as linked to the aggressiveness of PCa. Constitutional genetic variation of the FASN gene and the expression levels of FASN protein in cancer cells could thus be expected to predict outcome after radical prostatectomy (RP). This study evaluates the associations of malignant tissue status, neoadjuvant androgen deprivation therapy (NADT) and single-nucleotide polymorphisms (SNPs) of FASN with FASN protein expression in prostate tissue. The study then examines the associations of FASN SNPs and gene expression with three measures of post-prostatectomy outcome.
Seven tagging FASN SNPs were genotyped in 659 European American men who underwent RP at Roswell Park Cancer Institute between 1993 and 2005. FASN protein expression was assessed using immunohistochemistry. The patients were followed for an average of 6.9 years (range: 0.1-20.6 years). Outcome was assessed using three end points: biochemical failure, treatment failure and development of distant metastatic PCa. Cox proportional hazards analyses were used to evaluate the associations of the tagging SNPs and FASN expression with these end points. Bivariate associations with outcomes were considered; the associations also were controlled for known aggressiveness indicators.
Overall, no SNPs were associated with any known aggressiveness indicators. FASN staining intensity was stronger in malignant than in benign tissue, and NADT was associated with decreased FASN staining in both benign and malignant tissue. The relationships of FASN SNPs and staining intensity with outcome were less clear. One SNP, rs4246444, showed a weak association with outcome. FASN staining intensity also showed a weak and seemingly contradictory relationship with outcome.
Additional study with longer follow-up and populations that include more metastatic patients is warranted.
脂肪酸合酶(FASN)在前列腺癌细胞中选择性过表达,已被描述为与前列腺癌的侵袭性相关。因此,FASN基因的体质性遗传变异以及癌细胞中FASN蛋白的表达水平有望预测根治性前列腺切除术(RP)后的预后。本研究评估了FASN的恶性组织状态、新辅助雄激素剥夺治疗(NADT)和单核苷酸多态性(SNP)与前列腺组织中FASN蛋白表达的相关性。然后,该研究检查了FASN SNP和基因表达与前列腺切除术后三种预后指标的相关性。
对1993年至2005年间在罗斯威尔帕克癌症研究所接受RP的659名欧美男性进行了7个FASN标签SNP的基因分型。使用免疫组织化学评估FASN蛋白表达。对患者进行了平均6.9年的随访(范围:0.1 - 20.6年)。使用三个终点评估预后:生化失败、治疗失败和远处转移性前列腺癌的发生。使用Cox比例风险分析来评估标签SNP和FASN表达与这些终点的相关性。考虑了与预后的双变量相关性;这些相关性也针对已知的侵袭性指标进行了控制。
总体而言,并无可与任何已知侵袭性指标相关的SNP。FASN染色强度在恶性组织中比在良性组织中更强,并且NADT与良性和恶性组织中FASN染色的降低相关。FASN SNP与染色强度和预后的关系不太明确。一个SNP,rs4246444,与预后显示出微弱的相关性。FASN染色强度与预后也显示出微弱且看似矛盾的关系。
有必要进行更长随访时间以及纳入更多转移性患者的人群的进一步研究。