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ABSTRACT: Background
Hypoxia is a common characteristic of solid tumors associated with reduced response to radio- and chemotherapy, therefore increasing the probability of tumor recurrence. The aim of this study was to identify new mechanisms responsible for hypoxia-induced resistance in breast cancer cells.Methods
MDA-MB-231 and HepG2 cells were incubated in the presence of taxol or etoposide respectively under normoxia and hypoxia and apoptosis was analysed. A whole transcriptome analysis was performed in order to identify genes whose expression profile was correlated with apoptosis. The effect of gene invalidation using siRNA was studied on drug-induced apoptosis.Results
MDA-MB-231 cells incubated in the presence of taxol were protected from apoptosis and cell death by hy
SUBMITTER: Flamant L
PROVIDER: S-EPMC3519606 | biostudies-literature | 2012 Sep
REPOSITORIES: biostudies-literature