Gene expression profiling and molecular pathway analysis for the identification of early-stage lung adenocarcinoma patients at risk for early recurrence

被引:14
|
作者
Saji, Hisashi [1 ]
Tsuboi, Masahiro [1 ]
Shimada, Yoshihisa [1 ]
Kato, Yasufumi [1 ]
Hamanaka, Wakako [1 ]
Kudo, Yujin [1 ]
Yoshida, Koichi [1 ]
Matsubayashi, Jun [2 ]
Usuda, Jitsuo [1 ]
Ohira, Tatsuo [1 ]
Ikeda, Norihiko [1 ]
机构
[1] Tokyo Med Univ, Dept Surg, Div Thorac Surg, Shinjuku Ku, Tokyo 1600023, Japan
[2] Tokyo Med Univ, Dept Anat Pathol, Shinjuku Ku, Tokyo 1600023, Japan
关键词
lung adenocarcinoma; prognostic factor; microarray; molecular pathway analysis; early relapse; cell adhesion molecule; CANCER REGISTRY; PROGNOSIS; CELL; CLASSIFICATION; CARCINOMAS; MICROARRAY; SURVIVAL;
D O I
10.3892/or.2013.2332
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Clinicohistopathological staging is insufficient to predict disease progression and clinical outcome in lung carcinoma. Based on the results of the principal component analysis of 24 samples of early-stage lung adenocarcinoma, two subgroups were identified within the early-relapse group. The histological classification of all samples of group A was poorly differentiated, whereas one out of three in group B was poorly differentiated. DAVID functional annotation analysis revealed that the molecular pathways enriched in group A included those associated with cell adhesion molecules (CAMs), cell cycle and antigen processing and presentation, whereas those in group B included CAMs, T cell receptor signaling, cytokine-cytokine receptor interaction, toll-like receptor signaling, chemokine signaling, primary immunodeficiency and natural killer cell-mediated cytotoxicity. The CAM pathway was enriched in both groups. This comprehensive gene expression and functional pathway analysis identified a distinct molecular pathway, CAMs, that correlated with the early relapse of patients with early-stage lung adenocarcinoma.
引用
收藏
页码:1902 / 1906
页数:5
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