Mesenchymal stem cell-derived extracellular vesicles may promote breast cancer cell dormancy
journal contributionposted on 17.01.2019 by Jake Casson, Owen Davies, Carol-Anne Smith, Matthew J. Dalby, Catherine C. Berry
Any type of content formally published in an academic journal, usually following a peer-review process.
Disseminated breast cancer cells have the capacity to metastasise to the bone marrow and reside in a dormant state within the mesenchymal stem cell (MSC) niche. Research has focussed on paracrine signalling factors, such as soluble proteins, within the microenvironment. However, it is now clear extracellular vesicles (EVs) secreted by resident MSCs into this microenvironment also play a key role in the initiation of dormancy. Dormancy encourages reduced cell proliferation and migration, whilst upregulating cell adhesion, thus retaining the cancer cells within the bone marrow microenvironment. Here, MCF7 breast cancer cells were treated with MSC-derived EVs, resulting in reduced migration in 2D and 3D culture, with reduced cell proliferation and enhanced adhesion, collectively supporting cancer cell dormancy.
The authors would like to reference funding from the BBSRC for this work, grant reference number BB/L008661/1.
- Sport, Exercise and Health Sciences