TY - JOUR
T1 - Panels of tumor-derived RNA markers in peripheral blood of patients with non-small cell lung cancer
T2 - Their dependence on age, gender and clinical stages
AU - Chian, Chih Feng
AU - Hwang, Yi Ting
AU - Terng, Harn Jing
AU - Lee, Shih Chun
AU - Chao, Tsui Yi
AU - Chang, Hung
AU - Ho, Ching Liang
AU - Wu, Yi Ying
AU - Perng, Wann Cherng
PY - 2016
Y1 - 2016
N2 - Peripheral blood mononuclear cell (PBMC)-derived gene signatures were investigated for their potential use in the early detection of non-small cell lung cancer (NSCLC). In our study, 187 patients with NSCLC and 310 age- and gender-matched controls, and an independent set containing 29 patients for validation were included. Eight significant NSCLC-associated genes were identified, including DUSP6, EIF2S3, GRB2, MDM2, NF1, POLDIP2, RNF4, and WEE1. The logistic model containing these significant markers was able to distinguish subjects with NSCLC from controls with an excellent performance, 80.7% sensitivity, 90.6% specificity, and an area under the receiver operating characteristic curve (AUC) of 0.924. Repeated random subsampling for 100 times was used to validate the performance of classification training models with an average AUC of 0.92. Additional cross-validation using the independent set resulted in the sensitivity 75.86%. Furthermore, six age/gender-dependent genes: CPEB4, EIF2S3, GRB2, MCM4, RNF4, and STAT2 were identified using age and gender stratification approach. STAT2 and WEE1 were explored as stage-dependent using stage-stratified subpopulation. We conclude that these logistic models using different signatures for total and stratified samples are potential complementary tools for assessing the risk of NSCLC.
AB - Peripheral blood mononuclear cell (PBMC)-derived gene signatures were investigated for their potential use in the early detection of non-small cell lung cancer (NSCLC). In our study, 187 patients with NSCLC and 310 age- and gender-matched controls, and an independent set containing 29 patients for validation were included. Eight significant NSCLC-associated genes were identified, including DUSP6, EIF2S3, GRB2, MDM2, NF1, POLDIP2, RNF4, and WEE1. The logistic model containing these significant markers was able to distinguish subjects with NSCLC from controls with an excellent performance, 80.7% sensitivity, 90.6% specificity, and an area under the receiver operating characteristic curve (AUC) of 0.924. Repeated random subsampling for 100 times was used to validate the performance of classification training models with an average AUC of 0.92. Additional cross-validation using the independent set resulted in the sensitivity 75.86%. Furthermore, six age/gender-dependent genes: CPEB4, EIF2S3, GRB2, MCM4, RNF4, and STAT2 were identified using age and gender stratification approach. STAT2 and WEE1 were explored as stage-dependent using stage-stratified subpopulation. We conclude that these logistic models using different signatures for total and stratified samples are potential complementary tools for assessing the risk of NSCLC.
KW - Circulating tumor cells
KW - Gene expression profiling
KW - Non-small cell lung cancer
UR - http://www.scopus.com/inward/record.url?scp=84981357565&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84981357565&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.10558
DO - 10.18632/oncotarget.10558
M3 - Article
C2 - 27418131
AN - SCOPUS:84981357565
SN - 1949-2553
VL - 7
SP - 50582
EP - 50595
JO - Oncotarget
JF - Oncotarget
IS - 31
ER -