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CRISPR/Cas9 screening identifies a kinetochore-microtubule dependent mechanism for Aurora-A inhibitor resistance in breast cancer.

Ailin ChenShijun WenFang LiuZijian ZhangMeiling LiuYuanzhong WuBin HeMin YanTiebang KangEric W-F LamZi-Feng WangQuentin Liu
Published in: Cancer communications (London, England) (2021)
These findings establish Haspin as a synthetic lethal target and demonstrate CHR-6494 as a potential combinational drug for promoting the therapeutic effects of MLN8237 on breast cancer.
Keyphrases
  • crispr cas
  • genome editing
  • genome wide
  • risk assessment
  • drug induced
  • electronic health record