Ontology highlight
ABSTRACT: Background
While hypoxia has been well-studied in various tumor microenvironments, its role in cancer cell dormancy is poorly understood, in part due to a lack of well-established in vitro and in vivo models. Hypoxic conditions under conventional hypoxia chambers are relatively unstable and cannot be maintained during characterization outside the chamber since normoxic response is quickly established. To address this challenge, we report a robust in vitro cancer dormancy model under a hypoxia-mimicking microenvironment using cobalt chloride (CoCl2), a hypoxia-mimetic agent, which stabilizes hypoxia inducible factor 1-alpha (HIF1α), a major regulator of hypoxia signaling.Methods
We compared cellular responses to CoCl2 and true hypoxia (0.1% O2
SUBMITTER: Lee HR
PROVIDER: S-EPMC6091074 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature