Gene Expression Profiling Predicts the Development of Oral Cancer

被引:110
作者
Saintigny, Pierre [2 ]
Zhang, Li [3 ]
Fan, You-Hong [2 ]
El-Naggar, Adel K. [4 ]
Papadimitrakopoulou, Vassiliki A. [2 ]
Feng, Lei [5 ]
Lee, J. Jack [5 ]
Kim, Edward S. [2 ]
Hong, Waun Ki [2 ]
Mao, Li [1 ,2 ]
机构
[1] Univ Maryland, Sch Dent, Dept Oncol & Diagnost Sci, Baltimore, MD 21201 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Bioinformat & Computat Biol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
关键词
SQUAMOUS-CELL CARCINOMA; LUNG-CANCER; PREMALIGNANT LESIONS; HUMAN-PAPILLOMAVIRUS; SURVIVAL PREDICTION; HEAD; RISK; NECK; VALIDATION; CLASSIFICATION;
D O I
10.1158/1940-6207.CAPR-10-0155
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with oral premalignant lesion (OPL) have a high risk of developing oral cancer. Although certain risk factors, such as smoking status and histology, are known, our ability to predict oral cancer risk remains poor. The study objective was to determine the value of gene expression profiling in predicting oral cancer development. Gene expression profile was measured in 86 of 162 OPL patients who were enrolled in a clinical chemoprevention trial that used the incidence of oral cancer development as a prespecified endpoint. The median follow-up time was 6.08 years and 35 of the 86 patients developed oral cancer over the course. Gene expression profiles were associated with oral cancer-free survival and used to develop multivariate predictive models for oral cancer prediction. We developed a 29-transcript predictive model which showed marked improvement in terms of prediction accuracy (with 8% predicting error rate) over the models using previously known clinicopathologic risk factors. On the basis of the gene expression profile data, we also identified 2,182 transcripts significantly associated with oral cancer risk-associated genes (P value < 0.01; univariate Cox proportional hazards model). Functional pathway analysis revealed proteasome machinery, MYC, and ribosomal components as the top gene sets associated with oral cancer risk. In multiple independent data sets, the expression profiles of the genes can differentiate head and neck cancer from normal mucosa. Our results show that gene expression profiles may improve the prediction of oral cancer risk in OPL patients and the significant genes identified may serve as potential targets for oral cancer chemoprevention. Cancer Prev Res; 4(2); 218-29. (C)2011 AACR.
引用
收藏
页码:218 / 229
页数:12
相关论文
共 56 条
[1]   Small integrin-binding ligand N-linked glycoproteins (SIBLINGs): multifunctional proteins in cancer [J].
Bellahcene, Akeila ;
Castronovo, Vincent ;
Ogbureke, Kalu U. E. ;
Fisher, Larry W. ;
Fedarko, Neal S. .
NATURE REVIEWS CANCER, 2008, 8 (03) :212-226
[2]   Epidermal Growth Factor Receptor Expression and Gene Copy Number in the Risk of Oral Cancer [J].
Benchekroun, Mohammed Taoudi ;
Saintigny, Pierre ;
Thomas, Sufi M. ;
El-Naggar, Adel K. ;
Papadimitrakopoulou, Vassiliki ;
Ren, Hening ;
Lang, Wenhua ;
Fan, You-Hong ;
Huang, Jianhua ;
Feng, Lei ;
Lee, J. Jack ;
Kim, Edward S. ;
Hong, Waun Ki ;
Johnson, Faye M. ;
Grandis, Jennifer R. ;
Mao, Li .
CANCER PREVENTION RESEARCH, 2010, 3 (07) :800-809
[3]   Chemoprevention of human prostate cancer by oral administration of green tea catechins in volunteers with high-grade prostate intraepithelial neoplasia: A preliminary report from a one-year proof-of-principle study [J].
Bettuzzi, S ;
Brausi, M ;
Rizzi, F ;
Castagnetti, G ;
Peracchia, G ;
Corti, A .
CANCER RESEARCH, 2006, 66 (02) :1234-1240
[4]  
BHUTANI M, 2008, STAT PROBABIL LETT, V1, P39
[5]   Boosting for high-dimensional time-to-event data with competing risks [J].
Binder, Harald ;
Allignol, Arthur ;
Schumacher, Martin ;
Beyersmann, Jan .
BIOINFORMATICS, 2009, 25 (07) :890-896
[6]   The ubiquitin-mediated protein degradation pathway in cancer: therapeutic implications [J].
Burger, AM ;
Seth, AK .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (15) :2217-2229
[7]   An integrative pathway-based clinical-genomic model for cancer survival prediction [J].
Chen, Xi ;
Wang, Lily ;
Ishwaran, Hemant .
STATISTICS & PROBABILITY LETTERS, 2010, 80 (17-18) :1313-1319
[8]   Molecular classification of head and neck squamous cell carcinomas using patterns of gene expression [J].
Chung, CH ;
Parker, JS ;
Karaca, G ;
Wu, JY ;
Funkhouser, WK ;
Moore', D ;
Butterfoss, D ;
Xiang, D ;
Zonation, A ;
Yin, XY ;
Shockley, WW ;
Weissler, MC ;
Dressler, LG ;
Shores, CG ;
Yarbrough, WG ;
Perou, CM .
CANCER CELL, 2004, 5 (05) :489-500
[9]   Microarrays: retracing steps [J].
Coombes, Kevin R. ;
Wang, Jing ;
Baggerly, Keith A. .
NATURE MEDICINE, 2007, 13 (11) :1276-1277
[10]  
COOMBES KR, 1976, NAT MED, V13, P1277