DYNC1I2 and medulloblastoma: Bartl et al. have shown that HHIP-AS1 knockdown decreases the cell viability and proliferation of tumoral cells and increases the survival of medulloblastoma models by altering the mitotic spindle organization; the proliferative effect of HHIP-AS1 is mediated through the HHIP-AS1/miR-425-5p/DYNC1I2 axis [55].