Performance of gene expression-based single sample predictors for assessment of clinicopathological subgroups and molecular subtypes in cancers: a case comparison study in non-small cell lung cancer

被引:18
作者
Cirenajwis, Helena [1 ]
Lauss, Martin [1 ]
Planck, Maria [1 ]
Vallon-Christersson, Johan [1 ]
Staaf, Johan [2 ]
机构
[1] Lund Univ, Lund, Sweden
[2] Lund Univ, Expt Oncol, Lund, Sweden
关键词
single sample predictor; non-small cell lung cancer; classification; gene pair; molecular subtype; tumor histology; ADENOCARCINOMA; SIGNATURE; VALIDATION; SURVIVAL; CLASSIFICATION; LIMITATIONS; STAGE;
D O I
10.1093/bib/bbz008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The development of multigene classifiers for cancer prognosis, treatment prediction, molecular subtypes or clinicopathological groups has been a cornerstone in transcriptomic analyses of human malignancies for nearly two decades. However, many reported classifiers are critically limited by different preprocessing needs like normalization and data centering. In response, a new breed of classifiers, single sample predictors (SSPs), has emerged. SSPs classify samples in an N-of-1 fashion, relying on, e.g. gene rules comparing expression values within a sample. To date, several methods have been reported, but there is a lack of head-to-head performance comparison for typical cancer classification problems, representing an unmet methodological need in cancer bioinformatics. To resolve this need, we performed an evaluation of two SSPs [k-top-scoring pair classifier (kTSP) and absolute intrinsic molecular subtyping (AIMS)] for two case examples of different magnitude of difficulty in non-small cell lung cancer: gene expression-based classification of (i) tumor histology and (ii) molecular subtype. Through the analysis of similar to 2000 lung cancer samples for each case example (n = 1918 and n = 2106, respectively), we compared the performance of the methods for different sample compositions, training data set sizes, gene expression platforms and gene rule selections. Three main conclusions are drawn from the comparisons: both methods are platform independent, they select largely overlapping gene rules associated with actual underlying tumor biology and, for large training data sets, they behave interchangeably performance-wise. While SSPs like AIMS and kTSP offer new possibilities to move gene expression signatures/predictors closer to a clinical context, they are still importantly limited by the difficultness of the classification problem at hand.
引用
收藏
页码:729 / 740
页数:12
相关论文
共 38 条
[1]   switchBox: an R package for k-Top Scoring Pairs classifier development [J].
Afsari, Bahman ;
Fertig, Elana J. ;
Geman, Donald ;
Marchionni, Luigi .
BIOINFORMATICS, 2015, 31 (02) :273-274
[2]   Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses [J].
Bhattacharjee, A ;
Richards, WG ;
Staunton, J ;
Li, C ;
Monti, S ;
Vasa, P ;
Ladd, C ;
Beheshti, J ;
Bueno, R ;
Gillette, M ;
Loda, M ;
Weber, G ;
Mark, EJ ;
Lander, ES ;
Wong, W ;
Johnson, BE ;
Golub, TR ;
Sugarbaker, DJ ;
Meyerson, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13790-13795
[3]   Biomarker Discovery in Non-Small Cell Lung Cancer: Integrating Gene Expression Profiling, Meta-analysis, and Tissue Microarray Validation [J].
Botling, Johan ;
Edlund, Karolina ;
Lohr, Miriam ;
Hellwig, Birte ;
Holmberg, Lars ;
Lambe, Mats ;
Berglund, Anders ;
Ekman, Simon ;
Bergqvist, Michael ;
Ponten, Fredrik ;
Koenig, Andre ;
Fernandes, Oswaldo ;
Karlsson, Mats ;
Helenius, Gisela ;
Karlsson, Christina ;
Rahnenfuehrer, Joerg ;
Hengstler, Jan G. ;
Micke, Patrick .
CLINICAL CANCER RESEARCH, 2013, 19 (01) :194-204
[4]   A qualitative transcriptional signature to reclassify estrogen receptor status of breast cancer patients [J].
Cai, Hao ;
Guo, Wenbing ;
Zhang, Shuobo ;
Li, Na ;
Wang, Xianlong ;
Liu, Huaping ;
Chen, Rou ;
Wang, Shanshan ;
Guo, Zheng ;
Li, Jing .
BREAST CANCER RESEARCH AND TREATMENT, 2018, 170 (02) :271-277
[5]   An integrated genomic analysis of lung cancer reveals loss of DUSP4 in EGFR-mutant tumors [J].
Chitale, D. ;
Gong, Y. ;
Taylor, B. S. ;
Broderick, S. ;
Brennan, C. ;
Somwar, R. ;
Golas, B. ;
Wang, L. ;
Motoi, N. ;
Szoke, J. ;
Reinersman, J. M. ;
Major, J. ;
Sander, C. ;
Seshan, V. E. ;
Zakowski, M. F. ;
Rusch, V. ;
Pao, W. ;
Gerald, W. ;
Ladanyi, M. .
ONCOGENE, 2009, 28 (31) :2773-2783
[6]   Comprehensive molecular profiling of lung adenocarcinoma [J].
Collisson, Eric A. ;
Campbell, Joshua D. ;
Brooks, Angela N. ;
Berger, Alice H. ;
Lee, William ;
Chmielecki, Juliann ;
Beer, David G. ;
Cope, Leslie ;
Creighton, Chad J. ;
Danilova, Ludmila ;
Ding, Li ;
Getz, Gad ;
Hammerman, Peter S. ;
Hayes, D. Neil ;
Hernandez, Bryan ;
Herman, James G. ;
Heymach, John V. ;
Jurisica, Igor ;
Kucherlapati, Raju ;
Kwiatkowski, David ;
Ladanyi, Marc ;
Robertson, Gordon ;
Schultz, Nikolaus ;
Shen, Ronglai ;
Sinha, Rileen ;
Sougnez, Carrie ;
Tsao, Ming-Sound ;
Travis, William D. ;
Weinstein, John N. ;
Wigle, Dennis A. ;
Wilkerson, Matthew D. ;
Chu, Andy ;
Cherniack, Andrew D. ;
Hadjipanayis, Angela ;
Rosenberg, Mara ;
Weisenberger, Daniel J. ;
Laird, Peter W. ;
Radenbaugh, Amie ;
Ma, Singer ;
Stuart, Joshua M. ;
Byers, Lauren Averett ;
Baylin, Stephen B. ;
Govindan, Ramaswamy ;
Meyerson, Matthew ;
Rosenberg, Mara ;
Gabriel, Stacey B. ;
Cibulskis, Kristian ;
Sougnez, Carrie ;
Kim, Jaegil ;
Stewart, Chip .
NATURE, 2014, 511 (7511) :543-550
[7]   Validation of a Histology-Independent Prognostic Gene Signature for Early-Stage, Non-Small-Cell Lung Cancer Including Stage IA Patients [J].
Der, Sandy D. ;
Sykes, Jenna ;
Pintilie, Melania ;
Zhu, Chang-Qi ;
Strumpf, Dan ;
Liu, Ni ;
Jurisica, Igor ;
Shepherd, Frances A. ;
Tsao, Ming-Sound .
JOURNAL OF THORACIC ONCOLOGY, 2014, 9 (01) :59-64
[8]   Profiling cancer testis antigens in non-small-cell lung cancer [J].
Djureinovic, Dijana ;
Hallstrom, Bjorn M. ;
Horie, Masafumi ;
Mattsson, Johanna Sofia Margareta ;
La Fleur, Linnea ;
Fagerberg, Linn ;
Brunnstrom, Hans ;
Lindskog, Cecilia ;
Madjar, Katrin ;
Rahnenfuehrer, Joerg ;
Ekman, Simon ;
Stahle, Elisabeth ;
Koyi, Hirsh ;
Branden, Eva ;
Edlund, Karolina ;
Hengstler, Jan G. ;
Lambe, Mats ;
Saito, Akira ;
Botling, Johan ;
Ponten, Fredrik ;
Uhlen, Mathias ;
Micke, Patrick .
JCI INSIGHT, 2016, 1 (10)
[9]   A Comparative and Integrative Approach Identifies ATPase Family, AAA Domain Containing 2 as a Likely Driver of Cell Proliferation in Lung Adenocarcinoma [J].
Fouret, Robert ;
Laffaire, Julien ;
Hofman, Paul ;
Beau-Faller, Michele ;
Mazieres, Julien ;
Validire, Pierre ;
Girard, Philippe ;
Camilleri-Broeet, Sophie ;
Vaylet, Fabien ;
Leroy-Ladurie, Francois ;
Soria, Jean-Charles ;
Fouret, Pierre .
CLINICAL CANCER RESEARCH, 2012, 18 (20) :5606-5616
[10]  
Geman Donald, 2004, Stat Appl Genet Mol Biol, V3, pArticle19