通过合成剂量致死性来确定PLK1-过度表达癌症的可向漏洞

Chelsea E Cunningham1, Frederick S Vizeacoumar2, Yue Zhang1

  • 1Department of Oncology, College of Medicine, University of Saskatchewan, Saskatoon, SK S7N 5E5, Canada.

Cell genomics
|May 10, 2025
PubMed
概括

向IGF2BP2提供了针对染色体不稳定性 (CIN) 癌症的新策略. 抑制IGF2BP2降低了Polo样酶1 (PLK1) 水平,限制了CIN驱动的恶性瘤的瘤生长.