PLoS ONE · 2013 · 60 citations · 27 references
OncologyMedicineHigh ExpressionTumor ProgressionPathologyBronchial NeoplasmNsclc ProgressionTumor SuppressorCancer GeneticsNsclc Cell LinesCancer BiologyCell BiologyTumor MicroenvironmentLung CancerTumor Biology
The objective of the current study was to determine the clinical significance of junctional adhesion molecule A (JAM-A) in patients with non-small cell lung cancer (NSCLC) and the biological function of JAM-A in NSCLC cell lines. We showed that JAM-A is predominantly expressed in cell membranes and high expression of JAM-A occurred in 37% of lung tumor specimens compared to corresponding normal tissues. High expression of JAM-A was significantly correlated with TNM stage (P = 0.021), lymph node metastasis (P = 0.007), and decreased overall survival (P = 0.02), In addition, we observed that silencing JAM-A by small interfering RNA inhibited tumor cell proliferation and induced cell cycle arrest at the G1/S boundary. Western blotting analysis revealed that knockdown of JAM-A decreased the protein levels of cyclin D1, CDK4, 6, and P-Rb. Thus, JAM-A plays an important role in NSCLC progression.
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Junction Adhesion Molecule Is a Receptor for Reovirus
Erik S. Barton, J. Craig Forrest, Jodi L. Connolly et al. · Cell · 2001 · 635 citations · Full text
Human junction adhesion molecule regulates tight junction resealing in epithelia
Yuan Liu, Asma Nusrat, Frederick J. Schnell et al. · Journal of Cell Science · 2000 · 517 citations