Highly accurate two-gene classifier for differentiating gastrointestinal stromal tumors and leiomyosarcomas

被引:121
作者
Price, Nathan D.
Trent, Jonathan
El-Naggar, Adel K.
Cogdell, David
Taylor, Ellen
Hunt, Kelly K.
Pollock, Raphael E.
Hood, Leroy
Shmulevich, Ilya
Zhang, Wei
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Pathol, Unit 85, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Sarcoma Med Oncol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Surg Oncol, Houston, TX 77030 USA
[4] Inst Syst Biol, Seattle, WA 98103 USA
关键词
cancer; classification; diagnostic; machine learning; molecular signature;
D O I
10.1073/pnas.0611373104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gastrointestinal stromal tumor (GIST) has emerged as a clinically distinct type of sarcoma with frequent overexpression and mutation of the c-Kit oncogene and a favorable response to imatinib mesylate [also known as ST1571 (Gleevec)] therapy. However, a significant diagnostic challenge remains in the differentiation of GIST from leiomyosarcomas (LMSs). To improve on the diagnostic evaluation and to complement the immunohistochemical evaluation of these tumors, we performed a whole-genome gene expression study on 68 well characterized tumor samples. Using bioinformatic approaches, we devised a two-gene relative expression classifier that distinguishes between GIST and LMS with an accuracy of 99.3% on the microarray samples and an estimated accuracy of 97.8% on future cases. We validated this classifier by using RT-PCR on 20 samples in the microarray study and on an additional 19 independent samples, with 100% accuracy. Thus, our two-gene relative expression classifier is a highly accurate diagnostic method to distinguish between GIST and LMS and has the potential to be rapidly implemented in a clinical setting. The success of this classifier is likely due to two general traits, namely that the classifier is independent of data normalization and that it uses as simple an approach as possible to achieve this independence to avoid overfitting. We expect that the use of simple marker pairs that exhibit these traits will beof significant clinical use in a variety of contexts.
引用
收藏
页码:3414 / 3419
页数:6
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