Boman Karolina, Andersson Gustav, Wennersten Christoffer, Nodin Björn, Ahlgren Göran, Jirström Karin
Department of Clinical Sciences Lund, Division of Oncology and Pathology, Lund University, Lund, Sweden.
Department of Translational Medicine, Lund University, Malmö, Sweden.
Biomark Res. 2017 Mar 14;5:10. doi: 10.1186/s40364-017-0090-y. eCollection 2017.
Urothelial bladder cancer (UBC) is a disease that often is discovered when the tumour is non-muscle invasive, i.e. in Ta or T1 stage. Some patients will progress into muscle-invasive disease, a potentially deadly condition. Although there are some prognostic models, the need for prognostic and predictive biomarkers is considerate and urgent. Membranous expression of podocalyxin-like protein 1 (PODXL) and low expression of the RNA-binding motif 3 (RBM3) has previously been shown to be associated with an aggressive tumour phenotype and poor prognosis in several forms of cancer, including UBC. In this study, we sought to validate the prognostic impact of PODXL and RBM3 in an independent cohort of UBC.
Using tissue microarrays and immunohistochemistry, PODXL and RBM3 expression was evaluated in 272 incident UBC cases from the prospective, population-based cohort study Malmö Diet and Cancer. Kaplan-Meier analysis and Cox proportional hazards modelling were used to evaluate the prognostic impact of these markers on 5-year overall survival (OS).
In line with previous studies, both membranous PODXL expression and low RBM3 expression was significantly associated with disadvantageous clinicopathological features. Membranous PODXL expression was significantly associated with a reduced 5-year overall survival in the entire cohort (univariable HR 3.28; 95% CI 1.89-5.69), but this association did not remain significant in multivariable analysis. In T1 tumours, PODXL was significantly associated with reduced survival in univariable analysis (HR = 2.83; 95% CI 1.04-7.72) and borderline significant in multivariable analysis (HR = 2.60; 95% CI 0.91-7.39). Low RBM3 expression was an independent predictor of a reduced survival in the entire cohort (univariable HR 3.19; 95% CI 2.02-5.04, and multivariable HR 1.85; 95% CI 1.11-3.09), and in T1 tumours (univariable HR 2.64; 95% CI 1.11-6.27, and multivariable HR 2.63; 95% CI 1.01-6.84).
A link between membranous PODXL expression and clinically more aggressive tumours was further confirmed, but PODXL expression was not an independent prognostic biomarker in this study. Low RBM3 expression was validated as an independent factor of poor prognosis in UBC, including T1 disease. These findings suggest that these biomarkers could be useful in stratifying patients with non-muscle invasive disease for more aggressive first line treatment.
尿路上皮膀胱癌(UBC)通常在肿瘤为非肌层浸润性时被发现,即处于Ta或T1期。一些患者会进展为肌层浸润性疾病,这是一种潜在的致命状况。尽管存在一些预后模型,但对预后和预测生物标志物的需求仍然迫切。此前研究表明,足突融合蛋白样蛋白1(PODXL)的膜表达和RNA结合基序3(RBM3)的低表达与包括UBC在内的多种癌症的侵袭性肿瘤表型及不良预后相关。在本研究中,我们试图在一个独立的UBC队列中验证PODXL和RBM3的预后影响。
使用组织微阵列和免疫组织化学方法,对来自前瞻性、基于人群的队列研究“马尔默饮食与癌症”中的272例新发UBC病例的PODXL和RBM3表达进行评估。采用Kaplan-Meier分析和Cox比例风险模型评估这些标志物对5年总生存期(OS)的预后影响。
与先前研究一致,PODXL的膜表达和RBM3的低表达均与不利的临床病理特征显著相关。PODXL膜表达与整个队列中5年总生存期降低显著相关(单变量HR 3.28;95%CI 1.89 - 5.69),但在多变量分析中这种关联不再显著。在T1期肿瘤中,PODXL在单变量分析中与生存期降低显著相关(HR = 2.83;95%CI 1.04 - 7.72),在多变量分析中接近显著(HR = 2.60;95%CI 0.91 - 7.39)。RBM3低表达是整个队列(单变量HR 3.19;95%CI 2.02 - 5.04,多变量HR 1.85;95%CI 1.11 - 3.09)以及T1期肿瘤(单变量HR
2.64;95%CI 1.11 - 6.27,多变量HR 2.63;95%CI 1.01 - 6.84)生存期降低的独立预测因素。
进一步证实了PODXL膜表达与临床上侵袭性更强的肿瘤之间的联系,但在本研究中PODXL表达不是一个独立的预后生物标志物。RBM3低表达被验证为UBC包括T1期疾病预后不良的独立因素。这些发现表明,这些生物标志物可能有助于对非肌层浸润性疾病患者进行分层,以便采取更积极的一线治疗。