| Literature DB >> 23468017 |
Hisashi Saji1, Masahiro Tsuboi, Yoshihisa Shimada, Yasufumi Kato, Wakako Hamanaka, Yujin Kudo, Koichi Yoshida, Jun Matsubayashi, Jitsuo Usuda, Tatsuo Ohira, Norihiko Ikeda.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23468017 DOI: 10.3892/or.2013.2332
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906