University of Toronto researchers performed in vitro and in vivo experiments to investigate the role of the circular RNA circSKA3 in tumor development. They examined the effects of circSKA3 on mediating breast cancer metastasis. In vitro, the researchers found that the circular RNA circSKA3 was transferred between breast cancer cells, which was decreased by inhibiting exosome secretion. In vivo, circSKA3-containing exosomes potentiated tumor development and invasion that was inhibited by blocking exosome transmission. The ascites isolated from tumor-bearing mice or breast cancer patients showed high levels of circSKA3 and integrin β1. Single-cell culture and single-cell PCR showed that circSKA3 was heterogeneously expressed; the cells expressing higher levels of circSKA3 had a higher potential to form large colonies. This property was similar to c-myc, but circSKA3 expression had no correlation with c-myc levels. The effects of circSKA3 on cell migration and invasion appeared to predominate c-myc functions. By releasing circSKA3-containing exosomes to cancer cells expressing lower levels of circSKA3, the large colonies could regulate the activities of small colonies, enhancing tumor-forming capacity of the entire population. Thus, the researchers provide evidence that the transmission of circular RNAs in tumor-derived exosomes may allow for the maintenance of advantageous invasive sub-clones in breast cancer.
Promotion of tumor progression by exosome transmission of circular RNA
Du WW, Li X, Ma J et al. (2021) Promotion of tumor progression by exosome transmission of circular RNA circSKA3. Mol Ther Nucleic Acids [online preprint]. [abstract]