Expression profiles of osteosarcoma that can predict response to chemotherapy

被引:112
作者
Man, TK
Chintagumpala, M
Visvanathan, J
Shen, JH
Perlaky, L
Hicks, J
Johnson, M
Davino, N
Murray, J
Helman, L
Meyer, W
Triche, T
Wong, KK
Lau, CC
机构
[1] Texas Childrens Hosp, Baylor Coll Med, Texas Childrens Canc Ctr, Dept Pediat, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Baylor Coll Med, Dept Orthoped Surg, Houston, TX 77030 USA
[4] Cook Childrens Med Ctr, Ft Worth, TX USA
[5] NCI, Pediat Oncol Branch, Bethesda, MD 20892 USA
[6] Univ Oklahoma, Hlth Sci Ctr, Oklahoma City, OK USA
[7] Childrens Hosp Los Angeles, Los Angeles, CA 90027 USA
关键词
D O I
10.1158/0008-5472.CAN-05-0985
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Osteosarcoma is the most common malignant bone tumor in children. After initial diagnosis is made with a biopsy, treatment consists of preoperative chemotherapy followed by definitive surgery and postoperative chemotherapy. The degree of tumor necrosis in response to preoperative chemotherapy is a reliable prognostic factor and is used to guide the choice of postoperative chemotherapy. Patients with tumors, which reveal >= 90% necrosis (good responders), have a much better prognosis than those with <90% necrosis (poor responders). Despite previous attempts to improve the outcome of poor responders by modifying the postoperative chemotherapy, their prognosis remains poor. Therefore, there is a need to predict at the time of diagnosis patients' response to preoperative chemotherapy. This will provide the basis for developing potentially effective therapy that can be given at the outset for those who are likely to have a poor response. Here, we report the analysis of 34 pediatric osteosarcoma samples by expression profiling. Using parametric two-sample t test, we identified 45 genes that discriminate between good and poor responders (P < 0.005) in 20 definitive surgery samples. A support vector machine classifier was built using these predictor genes and was tested for its ability to classify initial biopsy samples. Five of six initial biopsy samples that had corresponding definitive surgery samples in the training set were classified correctly (83%; confidence interval, 36%, 100%). When this classifier was used to predict eight independent initial biopsy samples, there was 100% accuracy (confidence interval, 63%, 100%). Many of the predictor genes are implicated in bone development, drug resistance, and tumorigenesis.
引用
收藏
页码:8142 / 8150
页数:9
相关论文
共 54 条
[31]  
Ochi K, 2004, INT J ONCOL, V24, P647
[32]   DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features [J].
Paloneva, J ;
Mandelin, J ;
Kiialainen, A ;
Böhling, T ;
Prudlo, J ;
Hakola, P ;
Hatia, M ;
Konttinen, YT ;
Peltonen, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (04) :669-675
[33]   Evaluation of normalization methods for microarray [J].
Park, T ;
Yi, SG ;
Kang, SH ;
Lee, S ;
Lee, YS ;
Simon, R .
BMC BIOINFORMATICS, 2003, 4 (1)
[34]   Molecular classification of cancer types from microarray data using the combination of genetic algorithms and support vector machines [J].
Peng, SH ;
Xu, QH ;
Ling, XB ;
Peng, XN ;
Du, W ;
Chen, LB .
FEBS LETTERS, 2003, 555 (02) :358-362
[35]   Treatment of nonmetastatic osteosarcoma of the extremity with preoperative and postoperative chemotherapy: A report from the children's cancer group [J].
Provisor, AJ ;
Ettinger, LJ ;
Nachman, JB ;
Krailo, MD ;
Makley, JT ;
Yunis, EJ ;
Huvos, AG ;
Betcher, DL ;
Baum, ES ;
Kisker, CT ;
Miser, JS .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) :76-84
[36]   A paradigm for class prediction using gene expression profiles [J].
Radmacher, MD ;
McShane, LM ;
Simon, R .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2002, 9 (03) :505-511
[37]   A molecular signature of metastasis in primary solid tumors [J].
Ramaswamy, S ;
Ross, KN ;
Lander, ES ;
Golub, TR .
NATURE GENETICS, 2003, 33 (01) :49-54
[38]   DNA microarrays in clinical oncology [J].
Ramaswamy, S ;
Golub, TR .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (07) :1932-1941
[39]   RECONSTITUTION OF P53-UBIQUITINYLATION REACTIONS FROM PURIFIED COMPONENTS - THE ROLE OF HUMAN UBIQUITIN-CONJUGATING ENZYME UBC4 AND EG-ASSOCIATED PROTEIN (E6AP) [J].
ROLFE, M ;
BEERROMERO, P ;
GLASS, S ;
ECKSTEIN, J ;
BERDO, I ;
THEODORAS, A ;
PAGANO, M ;
DRAETTA, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3264-3268
[40]   Pitfalls in the use of DNA microarray data for diagnostic and prognostic classification [J].
Simon, R ;
Radmacher, MD ;
Dobbin, K ;
McShane, LM .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2003, 95 (01) :14-18