All four patient-derived cell lines (CUTO8, CUTO9, CUTO29, and YU1077) exhibited a clear trend in the increase of BCL2L11 mRNA after 24 h of treatment with alectinib, brigatinib, and lorlatinib (Fig. 2C ), correlating with the H3122 and H2228 cell lines data.
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Novel selective strategies targeting the BCL-2 family to enhance clinical efficacy in ALK-rearranged non-small cell lung cancer.
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