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Publication : FOXD3 suppresses tumor growth and angiogenesis in non-small cell lung cancer.

First Author  Yan JH Year  2015
Journal  Biochem Biophys Res Commun Volume  466
Issue  1 Pages  111-6
PubMed ID  26341266 Mgi Jnum  J:232873
Mgi Id  MGI:5780367 Doi  10.1016/j.bbrc.2015.08.116
Citation  Yan JH, et al. (2015) FOXD3 suppresses tumor growth and angiogenesis in non-small cell lung cancer. Biochem Biophys Res Commun 466(1):111-6
abstractText  The transcription factor forkhead box D3 (FOXD3), widely studied as a transcriptional repressor in embryogenesis, participates in the carcinogenesis of many cancers. However, the expression pattern and role of FOXD3 in non-small cell lung cancer (NSCLC) have not been well characterized. We report that FOXD3 is significantly downregulated in NSCLC cell lines and clinical tissues. FOXD3 overexpression significantly inhibits cell growth and results in G1 cell cycle arrest in NSCLC A549 and H1299 cells. In a xenograft tumor model, FOXD3 overexpression inhibits tumor growth and angiogenesis. Remarkably, expression of vascular endothelial growth factor (VEGF) was reduced in FOXD3 overexpression models both in vitro and in vivo. These findings suggest that FOXD3 plays a potential tumor suppressor role in NSCLC progression and represents a promising clinical prognostic marker and therapeutic target for this disease.
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