Department of Biochemistry and Molecular Biology, Faculty of Biology, National and Kapodostrian University of Athens, Athens, Greece.
First Department of Urology, "Laiko" General Hospital, Medical School, National and Kapodostrian University of Athens, Athens, Greece.
Br J Cancer. 2018 Dec;119(12):1477-1486. doi: 10.1038/s41416-018-0320-6. Epub 2018 Oct 30.
Bladder cancer (BlCa) heterogeneity and the lack of personalised prognosis lead to patients' highly variable treatment outcomes. Here, we have analysed the utility of the GAS5 tumour-suppressor lncRNA in improving BlCa prognosis.
GAS5 was quantified in a screening cohort of 176 patients. Hedegaard et al. (2016) (n = 476) and TCGA provisional (n = 413) were used as validation cohorts. Survival analysis was performed using recurrence and progression for NMIBC, or death for MIBC. Internal validation was performed by bootstrap analysis, and decision curve analysis was used to evaluate the clinical benefit on disease prognosis.
GAS5 levels were significantly downregulated in BlCa and associated with invasive high-grade tumours, and high EORTC-risk NMIBC patients. GAS5 loss was strongly and independently correlated with higher risk for NMIBC early relapse (HR = 2.680, p = 0.011) and progression (HR = 6.362, p = 0.035). Hedegaard et al. and TCGA validation cohorts' analysis clearly confirmed the association of GAS5 loss with NMIBC worse prognosis. Finally, multivariate models incorporating GAS5 with disease established markers resulted in higher clinical benefit for NMIBC prognosis.
GAS5 loss is associated with adverse outcome of NMIBC and results in improved positive prediction of NMIBC patients at higher risk for short-term relapse and progression, supporting personalised prognosis and treatment decisions.
膀胱癌(BlCa)的异质性和缺乏个性化预后导致患者的治疗结果差异很大。在这里,我们分析了 GAS5 肿瘤抑制 lncRNA 在改善膀胱癌预后方面的效用。
在 176 名患者的筛查队列中定量分析了 GAS5。Hedegaard 等人(2016 年)(n=476)和 TCGA 临时队列(n=413)被用作验证队列。使用非肌层浸润性膀胱癌(NMIBC)的复发和进展或肌层浸润性膀胱癌(MIBC)的死亡进行生存分析。通过自举分析进行内部验证,决策曲线分析用于评估对疾病预后的临床获益。
GAS5 水平在膀胱癌中显著下调,与侵袭性高级别肿瘤和高 EORTC 风险的 NMIBC 患者相关。GAS5 缺失与 NMIBC 早期复发(HR=2.680,p=0.011)和进展(HR=6.362,p=0.035)的高风险密切相关且独立相关。Hedegaard 等人和 TCGA 验证队列的分析清楚地证实了 GAS5 缺失与 NMIBC 预后不良的相关性。最后,将 GAS5 与疾病既定标志物纳入多变量模型可提高 NMIBC 预后的临床获益。
GAS5 缺失与 NMIBC 的不良结局相关,可提高对 NMIBC 患者短期复发和进展高风险的阳性预测,支持个性化预后和治疗决策。