Prognostic gene signatures for non-small-cell lung cancer

被引:157
作者
Boutros, Paul C. [1 ,5 ]
Lau, Suzanne K. [1 ,5 ]
Pintilie, Melania [5 ]
Liu, Ni [5 ]
Shepherd, Frances A. [2 ,6 ]
Der, Sandy D. [3 ,5 ]
Tsao, Ming-Sound [1 ,3 ,5 ]
Penn, Linda Z. [1 ,5 ]
Jurisica, Igor [1 ,4 ,5 ]
机构
[1] Univ Toronto, Dept Med Biophys, Toronto, ON M5S 1A1, Canada
[2] Univ Toronto, Dept Med, Toronto, ON M5S 1A1, Canada
[3] Univ Toronto, Dept Lab Med & Pathol, Toronto, ON M5S 1A1, Canada
[4] Univ Toronto, Dept Comp Sci, Toronto, ON M5S 1A1, Canada
[5] Univ Hlth Network, Ontario Canc Inst, Toronto, ON M5G 2M9, Canada
[6] Princess Margaret Hosp, Div Med Oncol, Toronto, ON M5G 2M9, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
biomarkers; systems biology; mRNA quantitation; substaging; VINORELBINE PLUS CISPLATIN; BREAST-CANCER; EXPRESSION SIGNATURES; SQUAMOUS-CELL; ADENOCARCINOMA; CLASSIFICATION; SURVIVAL; HETEROGENEITY; CHEMOTHERAPY; RECURRENCE;
D O I
10.1073/pnas.0809444106
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
Resectable non-small-cell lung cancer (NSCLC) patients have poor prognosis, with 30-50% relapsing within 5 years. Current staging criteria do not fully capture the complexity of this disease. Survival could be improved by identification of those early-stage patients who are most likely to benefit from adjuvant therapy. Molecular classification by using mRNA expression profiles has led to multiple, poorly overlapping signatures. We hypothesized that differing statistical methodologies contribute to this lack of overlap. To test this hypothesis, we analyzed our previously published quantitative RT-PCR dataset with a semisupervised method. A 6-gene signature was identified and validated in 4 independent public microarray datasets that represent a range of tumor histologies and stages. This result demonstrated that at least 2 prognostic signatures can be derived from this single dataset. We next estimated the total number of prognostic signatures in this dataset with a 10-million-signature permutation study. Our 6-gene signature was among the top 0.02% of signatures with maximum verifiability, reaffirming its efficacy. Importantly, this analysis identified 1,789 unique signatures, implying that our dataset contains > 500,000 verifiable prognostic signatures for NSCLC. This result appears to rationalize the observed lack of overlap among reported NSCLC prognostic signatures.
引用
收藏
页码:2824 / 2828
页数:5
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