Abstract
Based on cDNA microarray results, integrin-linked kinase (ILK) emerged as an interesting candidate in hypoxia-mediated survival mechanisms employed by cancer cells. This notion was confirmed here by the following observations: the 5′ promoter region of the ilk gene contains hypoxia responsive elements (HRE) that bind hypoxia-inducible factor (HIF) transcription factor complexes and drive HRE-luciferase gene expression in reporter assays; ILK protein and kinase activity are induced following hypoxia; downstream targets of ILK signaling are induced following hypoxia treatment; inhibition of ILK leads to increased apoptosis; and HIF and ILK are co-localized within human cancer tissues. The identification of ILK as a player in hypoxia survival signaling employed by cancer cells further validates ILK as a unique target for cancer therapy.
Author supplied keywords
Cite
CITATION STYLE
Abboud, E. R., Coffelt, S. B., Figueroa, Y. G., Zwezdaryk, K. J., Nelson, A. B., Sullivan, D. E., … Scandurro, A. B. (2007). Integrin-linked kinase: A hypoxia-induced anti-apoptotic factor exploited by cancer cells. International Journal of Oncology, 30(1), 113–122. https://doi.org/10.3892/ijo.30.1.113
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.