Park Jee Soo, Lee Hyo Jung, Cho Nam Hoon, Kim Jongchan, Jang Won Sik, Heo Ji Eun, Ham Won Sik
Department of Urology and Urological Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Department of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Comput Struct Biotechnol J. 2019 Mar 8;17:371-377. doi: 10.1016/j.csbj.2019.03.005. eCollection 2019.
Some early-stage clear cell renal cell carcinomas (ccRCCs) of ≤7 cm are associated with a poor clinical outcome. In this study, we investigated molecular biomarkers associated with aggressive clinical T1 stage ccRCCs of ≤7 cm, which were used to develop a risk prediction tool toward guiding the decision of treatment. Among 1069 nephrectomies performed for ccRCC of ≤7 cm conducted between January 2008 and December 2014, 177 cases with available formalin-fixed paraffin-embedded tissue were evaluated. An aggressive tumor was defined as a tumor exhibiting synchronous metastasis, recurrence, or leading to cancer-specific death. Expression levels of six genes (, and ) were measured by reverse-transcription polymerase chain reaction (qRT-PCR) and their relation to clinical outcomes was investigated. Immunohistochemistry was performed to validate the expression profiles of selected genes significantly associated with clinical outcomes in multivariate analysis. Using these genes, we developed a prediction model of aggressive ccRCC based on logistic regression and deep-learning methods. , and expression levels were significantly lower in aggressive ccRCC than non-aggressive ccRCC both in univariate and multivariate analysis. The immunohistochemistry result demonstrated the significant downregulation of , and expression in aggressive ccRCC. Adding immunohistochemical staining results to qRT-PCR, the aggressive ccRCC prediction models had the area under the curve (AUC) of 0.760 and 0.796 and accuracy of 0.759 and 0.852 using the logistic regression method and deep-learning method, respectively. Use of these biomarkers and the developed prediction model can help stratify patients with clinical T1 stage ccRCC.
一些直径≤7厘米的早期透明细胞肾细胞癌(ccRCC)具有较差的临床预后。在本研究中,我们调查了与直径≤7厘米的侵袭性临床T1期ccRCC相关的分子生物标志物,这些标志物被用于开发一种风险预测工具,以指导治疗决策。在2008年1月至2014年12月期间进行的1069例直径≤7厘米的ccRCC肾切除术病例中,对177例有可用福尔马林固定石蜡包埋组织的病例进行了评估。侵袭性肿瘤定义为表现出同步转移、复发或导致癌症特异性死亡的肿瘤。通过逆转录聚合酶链反应(qRT-PCR)测量六个基因(、和)的表达水平,并研究它们与临床结果的关系。进行免疫组织化学以验证在多变量分析中与临床结果显著相关的选定基因的表达谱。利用这些基因,我们基于逻辑回归和深度学习方法开发了侵袭性ccRCC的预测模型。在单变量和多变量分析中,侵袭性ccRCC中的、和表达水平均显著低于非侵袭性ccRCC。免疫组织化学结果显示侵袭性ccRCC中、和表达明显下调。将免疫组织化学染色结果添加到qRT-PCR中,侵袭性ccRCC预测模型使用逻辑回归方法和深度学习方法时的曲线下面积(AUC)分别为0.760和0.796,准确率分别为0.759和0.852。使用这些生物标志物和开发的预测模型有助于对临床T1期ccRCC患者进行分层。