Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, British Columbia, Canada.
Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Mol Cancer Ther. 2022 Feb;21(2):294-309. doi: 10.1158/1535-7163.MCT-21-0411. Epub 2021 Nov 23.
Androgen receptor (AR) has essential roles in the growth of prostate cancer and some breast cancers. Inhibition of AR transcriptional activity by targeting its N-terminal domain with ralaniten or an analog such as EPI-7170 causes accumulation of cells in the G-phase of the cell cycle. Inhibition of cyclin-dependent kinases 4/6 with palbociclib also leads to accumulation of cells in the G-phase. Here, a combination of EPI-7170 with palbociclib attenuated the growth of human castration-resistant prostate cancer xenografts that are resistant to antiandrogens. Cell-cycle tracing experiments in cultured cells revealed that EPI-7170 targeted cells in the S-phase, possibly through inducing DNA damage or impairing the DNA damage response, whereas palbociclib targeted the G-S transition to delay the cell cycle. Combination treatment prevented cells in G and G-M from progressing in the cell cycle and caused a portion of cells in the S-phase to arrest, which contributed to a twofold increase in doubling time to >63 hours compared with 25 hours in control cells. Importantly, sequential combination treatments with palbociclib administered first then followed by EPI-7170, resulted in more cells accumulating in G and less cells in the S-phase than concomitant combination which was presumably because each inhibitor has a unique mechanism in modulating the cell cycle in cancer cells. Together, these data support that the combination therapy was more effective than individual monotherapies to reduce tumor growth by targeting different phases of the cell cycle.
雄激素受体 (AR) 在前列腺癌和一些乳腺癌的生长中起关键作用。通过靶向 AR N 端结构域的 ralaniten 或类似物如 EPI-7170 抑制其转录活性会导致细胞在细胞周期的 G1 期积累。用 palbociclib 抑制周期蛋白依赖性激酶 4/6 也会导致细胞在 G1 期积累。在这里,EPI-7170 与 palbociclib 的联合使用减弱了对雄激素拮抗剂耐药的人去势抵抗性前列腺癌异种移植瘤的生长。在培养细胞中的细胞周期追踪实验表明,EPI-7170 靶向 S 期细胞,可能通过诱导 DNA 损伤或损害 DNA 损伤反应,而 palbociclib 靶向 G1-S 转换以延迟细胞周期。联合治疗阻止了 G1 和 G2-M 期细胞在细胞周期中的进展,并导致一部分 S 期细胞停滞,这导致倍增时间从对照细胞的 25 小时增加到 >63 小时,增加了两倍。重要的是,先用 palbociclib 序贯联合治疗,然后再用 EPI-7170 治疗,导致 G1 期积累的细胞更多,S 期细胞更少,而同时联合治疗则更少,这可能是因为每种抑制剂在调节癌细胞周期方面都具有独特的机制。总之,这些数据表明,联合治疗通过靶向细胞周期的不同阶段,比单独使用两种药物更有效地减少肿瘤生长。