Dinu Irina, Poudel Surya, Pyne Saumyadipta
School of Public Health, University of Alberta, Edmonton, AB, Canada.
Indian Institute of Public Health, Public Health Foundation of India, Hyderabad, India.
Cancer Inform. 2017 Sep 11;16:1176935117730016. doi: 10.1177/1176935117730016. eCollection 2017.
The Gleason score (GS) plays an important role in prostate cancer detection and treatment. It is calculated based on a sum between its major and minor components, each ranging from 1 to 5, assigned after examination of sample cells taken from each side of the prostate gland during biopsy. A total GS of at least 7 is associated with more aggressive prostate cancer. However, it is still unclear how prostate cancer outcomes differ for various distributions of GS between its major and minor components. This article applies Significance Analysis of Microarray for Gene-Set Reduction to a real microarray study of patients with prostate cancer and identifies 13 core genes differentially expressed between patients with a major GS of 3 and a minor GS of 4, or (3,4), vs patients with a combination of (4,3), starting from a less aggressive GS combination of (3,3), and moving toward a more aggressive one of (4,4) via gray areas of (3,4) and (4,3). The resulting core genes may improve understanding of prostate cancer in patients with a total GS of 7, the most common grade and most challenging with respect to prognosis.
Gleason评分(GS)在前列腺癌的检测和治疗中起着重要作用。它是根据其主要成分和次要成分的总和计算得出的,每个成分的范围从1到5,是在活检期间对从前列腺两侧采集的样本细胞进行检查后确定的。总GS至少为7与更具侵袭性的前列腺癌相关。然而,目前尚不清楚对于GS在其主要成分和次要成分之间的各种分布,前列腺癌的预后如何不同。本文将基因集缩减的微阵列显著性分析应用于一项针对前列腺癌患者的实际微阵列研究,并从侵袭性较小的GS组合(3,3)开始,通过(3,4)和(4,3)的灰色区域,向侵袭性更强的(4,4)组合发展,确定了主要GS为3且次要GS为4(即(3,4))的患者与(4,3)组合的患者之间差异表达的13个核心基因。所得出的核心基因可能会增进对总GS为7的前列腺癌患者的理解,这是最常见的分级,也是预后方面最具挑战性的。