Journal of Stem Cell Research & Therapy

Bone marrow mesenchymal stem cells differentially affect the aggressiveness of cancer cell subtypes

9^th Annual Conference on Stem Cell and Regenerative Medicine

September 25-26, 2017 Berlin, Germany

Tamara Lah Turnsek

Mednarodna podiplomska sola Jozefa Stefana, Slovenia

Scientific Tracks Abstracts: J Stem Cell Res Ther

Abstract:

The most aggressive brain tumour glioblastoma multiforme is characterized by aggressive Glioblastoma (GBM) cell infiltration into surrounding brain parenchyma. We hypothesise that this invasion process is supported by Mesenchymal Stem Cells (MSCs), comprising GBM microenvironment. MSCs are recruited from bone marrow or endogenous brain tissue to the GBM tumour, but their interactions with GBM cells are still poorly understood. To elucidate the direct interaction between bone marrow-derived MSCs and two distinct GBM cell lines, U87 and U373, we tested cells�?? invasion in vitro, as well as in vivo, using zebrafish embryo model. Since proteases are crucial for GBM cell invasion, we focused on their role in invasion of cells in MSC/GBM direct co-cultures by analysing their expression at gene and protein levels and by applying selective protease inhibitors in the 3D-invasion model in vitro. We demonstrated that the effect of MSC/GBM cellular cross-talk on GBM cell invasion is GBM cell type specific. Namely, MSCs decreased the invasion of U87 cells, whereas they increased the invasion of U373 cells in vitro and in vivo. In contrast, both GBM cell lines increased the invasiveness of MSCs upon direct interactions. Moreover, we observed that increased U373 cell invasion in co-cultures correlated with increased expression of cathepsin B, calpain1, uPA/uPAR, MMP-9 and -14, all involved in the protease signalling cascade in GBM cells, leading to increased invasion via extracellular matrix degradation. Using selective inhibitors, we confirmed involvement of cathepsin B, MMP-9 and -14 in MSC-enhanced invasion of U373 cells. By contrast, decreased invasion of U87 upon co-culturing seemed to be independent of these proteases, implicating that the MSC regulatory potential in MSC/GBM co-cultures is dependent on GBM phenotype. Finally, we identified the genes, associated with cell response to TGF-�? that were differentially expressed in U87 vs. U373 cells that could explain different response of these cell lines to MSCs. Taken together, our findings are the first to suggest that the response of GBM cells to MSCs depends on the cancer cell�??s genetic subtype. This notion may be generalized to other types of stromal cells as well as to other tumours.

Biography :

Tamara Lah Turnšek has completed her graduation (organic chemistry), magisterium (biochemistry) and doctorate (biochemistry), she worked at the Department of Biochemistry and Molecular Biology at the Jožef Stefan Institute and for quite a while likewise at the Clinical Laboratory of the Paediatric Clinic in Ljubljana. Since 1996, she has been Director of the National Institute of Biology, where in the vicinity of 1997 and 2004 she additionally filled in as Head of the Department of Genetic Toxicology and Cancer Biology.