As expected, treatment with 30 μM carboplatin for 72 h decreased the proportion of cells in the G1 phase approaching significance, and significantly increased the proportion of cells in the S phase compared to DMSO vehicle.
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Repurposing of ivacaftor shows potential to treat ROR1 expressing high-grade serous ovarian cancer.
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Interestingly, ROR1 knockout KURAMOCHI cells still showed a trend towards reduced signalling upon ivacaftor treatment.
KURAMOCHI ROR1 KO cell lines showed a very similar trend for ivacaftor treatment compared to vehicle control, but the trends did not reach statistical significance.