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Design, synthesis, and characterization of PROTACs targeting the androgen receptor in prostate and lung cancer models [Elektronski vir]Gockel, Lukas Maria ...Although the androgen receptor (AR) is a validated target for the treatment of prostate cancer, resistance to antiandrogens necessitates the development of new therapeutic modalities. Exploiting the ... ubiquitin-proteasome system with proteolysis-targeting chimeras (PROTACs) has become a practical approach to degrade specific proteins and thus to extend the portfolio of small molecules used for the treatment of a broader spectrum of diseases. Herein, we present three subgroups of enzalutamide-based PROTACs in which only the exit vector was modified. By recruiting cereblon, we were able to demonstrate the potent degradation of AR in lung cancer cells. Furthermore, the initial evaluation enabled the design of an optimized PROTAC with a rigid linker that degraded AR with a DC50 value in the nanomolar range. These results provide novel AR-directed PROTACs and a clear rationale for further investigating AR involvement in lung cancer models.Vir: Archiv der Pharmazie [Elektronski vir]. - ISSN 1521-4184 (Vol. 355, iss. 5, e2100467, 2022, str. 1-15)Vrsta gradiva - e-članek ; neleposlovje za odrasleLeto - 2022Jezik - angleškiCOBISS.SI-ID - 96807683
Avtor
Gockel, Lukas Maria |
Pfeifer, Vladlena |
Baltes, Fabian |
Bachmaier, Rafael D. |
Wagner, Karl G. |
Bendas, Gerd |
Gütschow, Michael |
Sosič, Izidor |
Steinebach, Christian
Teme
Farmacevtska kemija |
Rak (medicina) |
androgen receptor |
CRBN |
enzalutamide |
medicinal chemistry |
PROTAC |
androgeni receptor |
enzalutamid |
medicinska kemija
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Gockel, Lukas Maria | ![]() |
Pfeifer, Vladlena | ![]() |
Baltes, Fabian | ![]() |
Bachmaier, Rafael D. | ![]() |
Wagner, Karl G. | ![]() |
Bendas, Gerd | ![]() |
Gütschow, Michael | ![]() |
Sosič, Izidor | 30816 |
Steinebach, Christian | ![]() |
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