Improved grading and survival prediction of human astrocytic brain tumors by artificial neural network analysis of gene expression microarray data

被引:60
作者
Petalidis, Lawrence P. [2 ]
Oulas, Anastasis [1 ,3 ]
Backlund, Magnus [6 ]
Wayland, Matthew T. [4 ]
Liu, Lu [2 ]
Plant, Karen [2 ]
Happerfield, Lisa [2 ]
Freeman, Tom C. [5 ]
Poirazi, Panayiota [1 ]
Collins, V. Peter [2 ]
机构
[1] Fdn Res & Technol Hellas, Inst Mol Biol & Biotechnol, GR-71110 Iraklion, Greece
[2] Univ Cambridge, Addenbrookes Hosp, Dept Pathol, Div Mol Histopathol, Cambridge CB2 2QQ, England
[3] Univ Crete, Dept Biol, Grad Program Mol Biol & Biomed, Iraklion, Crete, Greece
[4] Univ Cambridge, Cambridge Ctr Neuropsychiat Res, Cambridge, England
[5] Univ Edinburgh, Coll Med, Div Pathway, Edinburgh, Midlothian, Scotland
[6] Karolinska Inst, Karolinska Hosp, Dept Oncol Pathol, S-10401 Stockholm, Sweden
基金
英国医学研究理事会;
关键词
D O I
10.1158/1535-7163.MCT-07-0177
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Histopathologic grading of astrocytic tumors based on current WHO criteria offers a valuable but simplified representation of oncologic reality and is often insufficient to predict clinical outcome. In this study, we report a new astrocytic tumor microarray gene expression data set (n = 65). We have used a simple artificial neural network algorithm to address grading of human astrocytic tumors, derive specific transcriptional signatures from histopathologic subtypes of astrocytic tumors, and asses whether these molecular signatures define survival prognostic subclasses, Fifty-nine classifier genes were identified and found to fall within three distinct functional classes, that is, angiogenesis, cell differentiation, and lower-grade astrocytic tumor discrimination. These gene classes were found to characterize three molecular tumor subtypes denoted ANGIO, INTER, and LOWER. Grading of samples using these subtypes agreed with prior histopathologic grading for both our data set (96.15%) and an independent data set. Six tumors were particularly challenging to diagnose histopathologically. We present an artificial neural network grading for these samples and offer an evidence-based interpretation of grading results using clinical metadata to substantiate findings. The prognostic value of the three identified tumor subtypes was found to outperform histopathologic grading as well as tumor subtypes reported in other studies, indicating a high survival prognostic potential for the 59 gene classifiers. Finally, 11 gene classifiers that differentiate between primary and secondary glioblastomas were also identified.
引用
收藏
页码:1013 / 1024
页数:12
相关论文
共 38 条
[1]  
[Anonymous], 2000, World Health Organisation Classification of Tumours: Pathology and genetics of tumours of the nervous system
[2]  
Barrett T, 2005, NUCLEIC ACIDS RES, V33, pD562
[3]   The immunohistochemical expression of calcitonin receptor-like receptor (CRLR) in human gliomas [J].
Benes, L ;
Kappus, C ;
McGregor, GP ;
Bertalanffy, H ;
Mennel, HD ;
Hagner, S .
JOURNAL OF CLINICAL PATHOLOGY, 2004, 57 (02) :172-176
[4]  
BURGER P, 1994, ATLAS TUMOR PATHOLOG
[5]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[6]  
EKSTRAND AJ, 1991, CANCER RES, V51, P2164
[7]   Gene expression profiling of gliomas strongly predicts survival [J].
Freije, WA ;
Castro-Vargas, FE ;
Fang, ZX ;
Horvath, S ;
Cloughesy, T ;
Liau, LM ;
Mischel, PS ;
Nelson, SF .
CANCER RESEARCH, 2004, 64 (18) :6503-6510
[8]   PEA-15 is inhibited by adenovirus E1A and plays a role in ERK nuclear export and Ras-induced senescence [J].
Gaumont-Leclerc, MF ;
Mukhopadhyay, UK ;
Goumard, S ;
Ferbeyre, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (45) :46802-46809
[9]   Bioconductor: open software development for computational biology and bioinformatics [J].
Gentleman, RC ;
Carey, VJ ;
Bates, DM ;
Bolstad, B ;
Dettling, M ;
Dudoit, S ;
Ellis, B ;
Gautier, L ;
Ge, YC ;
Gentry, J ;
Hornik, K ;
Hothorn, T ;
Huber, W ;
Iacus, S ;
Irizarry, R ;
Leisch, F ;
Li, C ;
Maechler, M ;
Rossini, AJ ;
Sawitzki, G ;
Smith, C ;
Smyth, G ;
Tierney, L ;
Yang, JYH ;
Zhang, JH .
GENOME BIOLOGY, 2004, 5 (10)
[10]  
Godard S, 2003, CANCER RES, V63, P6613