| Literature DB >> 16427189 |
Sang-Min Lee1, Choon-Taek Lee, Young Whan Kim, Sung Koo Han, Young-Soo Shim, Chul-Gyu Yoo.
Abstract
Hypoxia confers protection against apoptosis in cancer cells, and this hypoxia-induced resistance to apoptosis has been suggested to be associated with genetic and adaptive changes. However, it is not clear whether survival signals, such as the PI3K/Akt and ERK pathways are involved. We investigated the roles of these pathways in hypoxia-induced protection against apoptosis in lung cancer cells. Treatment of cells with either ultraviolet (UV) or etoposide induced apoptosis time-dependently in A549 and NCI-H157 cells. However, though hypoxia alone neither induced apoptosis nor reduced cell survival, it suppressed the apoptosis induced by UV or etoposide. Moreover, hypoxia activated the PI3K/Akt and ERK pathways, and blocking the activation of either pathway reversed resistance to UV- and etoposide-induced apoptosis in response to hypoxia. These results suggest that hypoxia confers resistance to UV- or etoposide-mediated apoptosis in lung cancer cells via the activations of the PI3K/Akt and the ERK pathways.Entities:
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Year: 2006 PMID: 16427189 DOI: 10.1016/j.canlet.2005.11.001
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679