Department of Internal Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, MO, USA; Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, MO, USA.
Department of Radiation Oncology, University of Michigan Medical School, Ann Arbor, MI, USA; Beaumont Hospital-Dearborn, Transitional Year Program, Dearborn, MI, USA.
Eur Urol. 2017 Feb;71(2):257-266. doi: 10.1016/j.eururo.2016.07.012. Epub 2016 Jul 22.
Long noncoding RNAs (lncRNAs) are an emerging class of relatively underexplored oncogenic molecules with biological and clinical significance. Current inadequacies for stratifying patients with aggressive disease presents a strong rationale to systematically identify lncRNAs as clinical predictors in localized prostate cancer.
To identify RNA biomarkers associated with aggressive prostate cancer.
DESIGN, SETTING, AND PARTICIPANTS: Radical prostatectomy microarray and clinical data was obtained from 910 patients in three published institutional cohorts: Mayo Clinic I (N=545, median follow-up 13.8 yr), Mayo Clinic II (N=235, median follow-up 6.7 yr), and Thomas Jefferson University (N=130, median follow-up 9.6 yr).
The primary clinical endpoint was distant metastasis-free survival. Secondary endpoints include prostate cancer-specific survival and overall survival. Univariate and multivariate Cox regression were used to evaluate the association of lncRNA expression and these endpoints.
An integrative analysis revealed Prostate Cancer Associated Transcript-14 (PCAT-14) as the most prevalent lncRNA that is aberrantly expressed in prostate cancer patients. Down-regulation of PCAT-14 expression significantly associated with Gleason score and a greater probability of metastatic progression, overall survival, and prostate cancer-specific mortality across multiple independent datasets and ethnicities. Low PCAT-14 expression was implicated with genes involved in biological processes promoting aggressive disease. In-vitro analysis confirmed that low PCAT-14 expression increased migration while overexpressing PCAT-14 reduced cellular growth, migration, and invasion.
We discovered that androgen-regulated PCAT-14 is overexpressed in prostate cancer, suppresses invasive phenotypes, and lower expression is significantly prognostic for multiple clinical endpoints supporting its significance for predicting metastatic disease that could be used to improve patient management.
We discovered that aberrant prostate cancer associated transcript-14 expression during prostate cancer progression is prevalent across cancer patients. Prostate cancer associated transcript-14 is also prognostic for metastatic disease and survival highlighting its importance for stratifying patients that could benefit from treatment intensification.
长非编码 RNA(lncRNA)是一类新兴的具有生物学和临床意义的致癌分子,目前对其研究还不够充分。因此,迫切需要寻找一种能够对侵袭性疾病进行分类的方法,以改善患者的治疗效果。目前,lncRNA 作为局部前列腺癌的临床预测因子已得到系统的确认。
寻找与侵袭性前列腺癌相关的 RNA 生物标志物。
设计、地点和参与者:从三个已发表的机构队列的 910 名患者中获取了根治性前列腺切除术的微阵列和临床数据:梅奥诊所 I(N=545,中位随访 13.8 年)、梅奥诊所 II(N=235,中位随访 6.7 年)和托马斯杰斐逊大学(N=130,中位随访 9.6 年)。
主要临床终点是远处无转移生存。次要终点包括前列腺癌特异性生存和总生存。采用单变量和多变量 Cox 回归分析评估 lncRNA 表达与这些终点的相关性。
综合分析显示,前列腺癌相关转录物 14(PCAT-14)是最常见的 lncRNA,在前列腺癌患者中表达异常。PCAT-14 表达下调与 Gleason 评分显著相关,与多个独立数据集和种族的转移进展、总生存和前列腺癌特异性死亡率的概率增加显著相关。PCAT-14 表达降低与促进侵袭性疾病的生物学过程相关基因有关。体外分析证实,低 PCAT-14 表达可促进迁移,而过表达 PCAT-14 则可降低细胞生长、迁移和侵袭。
我们发现雄激素调节的 PCAT-14 在前列腺癌中过度表达,抑制侵袭表型,低表达与多个临床终点显著相关,支持其对预测转移性疾病的意义,可用于改善患者管理。
我们发现,在前列腺癌进展过程中,异常的前列腺癌相关转录物 14 表达在癌症患者中普遍存在。前列腺癌相关转录物 14 对转移性疾病和生存也具有预后意义,突出了其在分层患者中的重要性,这可能有助于治疗的强化。