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Cyclin-dependent Kinase 4/6 Inhibitor Palbociclib in Combination with Ralaniten Analogs for the Treatment of Androgen
Amy H Tien1, Marianne D Sadar2,3
1Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, British Columbia, Canada.
Abstract:
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 G1-phase of the cell cycle. Inhibition of cyclin-dependent kinases 4/6 with palbociclib also leads to accumulation of cells in the G1-phase. Here, a combination of EPI-7170 with palbociclib attenuated the in vivo 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 G1-S transition to delay the cell cycle. Combination treatment prevented cells in G1 and G2-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 G1 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.
Insights
Combining EPI-7170 and palbociclib effectively inhibits prostate cancer growth by targeting different cell cycle phases. This combination therapy offers a promising strategy against antiandrogen-resistant cancers.
Area of Science:
- Oncology
- Molecular Biology
- Cell Cycle Regulation
Background:
- Androgen receptor (AR) signaling drives prostate and some breast cancers.
- AR inhibitors like EPI-7170 and cyclin-dependent kinase 4/6 (CDK4/6) inhibitors like palbociclib target cell cycle progression.
Purpose of the Study:
- To investigate the efficacy of combining EPI-7170 and palbociclib against antiandrogen-resistant prostate cancer.
- To elucidate the cell cycle mechanisms underlying the combination therapy's effects.
Main Methods:
- Treatment of human castration-resistant prostate cancer xenografts with EPI-7170 and palbociclib, alone and in combination.
- Cell-cycle tracing experiments in cultured cancer cells to analyze drug effects on cell cycle phase distribution.
Main Results:
- Combination therapy significantly attenuated tumor growth in vivo.
- EPI-7170 induced S-phase arrest, potentially via DNA damage, while palbociclib inhibited the G1-S transition.
- Combined treatment led to cell accumulation in G1 and G2-M phases and S-phase arrest, doubling tumor doubling time.
Conclusions:
- Combination therapy targeting distinct cell cycle phases is more effective than monotherapy for reducing tumor growth.
- Sequential administration of palbociclib followed by EPI-7170 demonstrated distinct cell cycle modulation compared to concomitant treatment.
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