Ontology highlight
ABSTRACT: Background
Breast cancers can recur after a long latency period following 'successful' primary treatments. Chronic inflammation significantly correlates with reduced diseased-free survival in breast cancer patients and could be a point of intervention to prevent recurrence. Liver is among the main sites of breast cancer recurrence. Thus, we hypothesise that inflammatory signals from hepatic stellate cells, the major inflammatory regulators in the sinusoid, could stimulate dormant cancer cells to emerge.Methods
We utilise in vitro co-culture of breast cancer cells with stellate cells and an ex vivo 3D human liver micro-physiologic system to identify stellate cells-derived factors that mediate tumour emergence.Results
Activated, but not quiescent, hepatic stellate cel
SUBMITTER: Khazali AS
PROVIDER: S-EPMC5830588 | biostudies-literature | 2018 Feb
REPOSITORIES: biostudies-literature