Co-Expression of CD34, CD90, OV-6 and Cell-Surface Vimentin Defines Cancer Stem Cells of Hepatoblastoma, Which Are Affected by Hsp90 Inhibitor 17-AAG.
Mieun Lee-TheilenJulia R HadhoudGiulietta VolanteDelaine D FadiniJulia EichhornUdo RolleHenning C FiegelPublished in: Cells (2021)
Cancer stem cells (CSCs) are nowadays one of the major focuses in tumor research since this subpopulation was revealed to be a great obstacle for successful treatment. The identification of CSCs in pediatric solid tumors harbors major challenges because of the immature character of these tumors. Here, we present CD34, CD90, OV-6 and cell-surface vimentin (csVimentin) as reliable markers to identify CSCs in hepatoblastoma cell lines. We were able to identify CSC characteristics for the subset of CD34+CD90+OV-6+csVimentin+-co-expressing cells, such as pluripotency, self-renewal, increased expression of EMT markers and migration. Treatment with Cisplatin as the standard chemotherapeutic drug in hepatoblastoma therapy further revealed the chemo-resistance of this subset, which is a main characteristic of CSCs. When we treated the cells with the Hsp90 inhibitor 17-AAG, we observed a significant reduction in the CSC subset. With our study, we identified CSCs of hepatoblastoma using CD34, CD90, OV-6 and csVimentin. This set of markers could be helpful to estimate the success of novel therapeutic approaches, as resistant CSCs are responsible for tumor relapses.
Keyphrases
- cancer stem cells
- cell surface
- induced apoptosis
- poor prognosis
- cell cycle arrest
- heat shock protein
- single cell
- heat stress
- heat shock
- emergency department
- cell death
- epithelial mesenchymal transition
- squamous cell carcinoma
- mesenchymal stem cells
- radiation therapy
- pi k akt
- drug delivery
- newly diagnosed
- cell proliferation
- young adults
- adverse drug