It is needed to explore novel
biological markers for early diagnosis and treatment of human
osteosarcoma.
Sphingosine kinase 2 (SphK2) expression and potential functions in
osteosarcoma were studied. We demonstrate that SphK2 is over-expressed in multiple human
osteosarcoma tissues and established human
osteosarcoma cell lines. Silence of SphK2 by targeted-shRNAs inhibited
osteosarcoma cell growth, and induced cell apoptosis. On the other hand, exogenous over-expression of SphK2 could further promote
osteosarcoma cell growth. Notably, microRNA-19a-3p ("miR-19a-3p") targets the
3' UTR (
untranslated region) of SphK2
mRNA. Remarkably, forced-expression of miR-19a-3p silenced SphK2 and inhibited
osteosarcoma cell growth. In vivo, SphK2 silence, by targeted-
shRNA or miR-19a-3p, inhibited U2OS
tumor growth in nude mice. These results suggest that SphK2 could be a novel and key oncotarget
protein for OS cell progression.