Antitumor activity of NLG207 (formerly CRLX101) in combination with enzalutamide in preclinical prostate cancer models
KT Schmidt, CH Chau, JD Strope, ADR Huitema… - Molecular cancer …, 2021 - AACR
Effective treatments for patients with metastatic castration-resistant prostate cancer following
disease progression on enzalutamide are currently an unmet clinical need. Simultaneous …
disease progression on enzalutamide are currently an unmet clinical need. Simultaneous …
The retinamide VNLG‐152 inhibits f‐AR/AR‐V7 and MNK–eIF 4E signaling pathways to suppress EMT and castration‐resistant prostate cancer xenograft growth
VP Ramamurthy, S Ramalingam, LK Gediya… - The FEBS …, 2018 - Wiley Online Library
VNLG‐152 is a novel retinamide (NR) shown to suppress growth and progression of
genetically diverse prostate cancer cells via inhibition of androgen receptor signaling and …
genetically diverse prostate cancer cells via inhibition of androgen receptor signaling and …
A single-arm phase II study combining NLG207, a nanoparticle camptothecin, with enzalutamide in advanced metastatic castration-resistant prostate cancer post …
Background Despite the clinical efficacy of enzalutamide monotherapy in patients with
advanced prostate cancer, therapeutic resistance and disease progression are inevitable …
advanced prostate cancer, therapeutic resistance and disease progression are inevitable …
Dual targeting of the androgen receptor and hypoxia-inducible factor 1α pathways synergistically inhibits castration-resistant prostate cancer cells
EV Fernandez, KM Reece, AM Ley, SM Troutman… - Molecular …, 2015 - ASPET
Enzalutamide is a potent second-generation androgen receptor (AR) antagonist with activity
in metastatic castrate-resistant prostate cancer (CRPC). Although enzalutamide is initially …
in metastatic castrate-resistant prostate cancer (CRPC). Although enzalutamide is initially …
Therapeutic potential of leelamine, a novel inhibitor of androgen receptor and castration-resistant prostate cancer
KB Singh, X Ji, SV Singh - Molecular cancer therapeutics, 2018 - AACR
Clinical management of castration-resistant prostate cancer (CRPC) resulting from
androgen deprivation therapy remains challenging. CRPC is driven by aberrant activation of …
androgen deprivation therapy remains challenging. CRPC is driven by aberrant activation of …
Design, Synthesis, and Evaluation of Niclosamide Analogs as Therapeutic Agents for Enzalutamide-Resistant Prostate Cancer
Niclosamide effectively downregulates androgen receptor variants (AR-Vs) for treating
enzalutamide and abiraterone-resistant prostate cancer. However, the poor pharmaceutical …
enzalutamide and abiraterone-resistant prostate cancer. However, the poor pharmaceutical …
Targeting prostate cancer cells with enzalutamide‐HDAC inhibitor hybrid drug 2‐75
Background The progression of castration‐resistant prostate cancer (CRPC) still relies on
the function of androgen receptor (AR), achieved by evolving mechanisms to reactivate AR …
the function of androgen receptor (AR), achieved by evolving mechanisms to reactivate AR …
[HTML][HTML] Fulvestrant increases the susceptibility of enzalutamide-resistant prostate cancer cells to NK-mediated lysis
M Dahut, K Fousek, LA Horn, S Angstadt… - … for Immunotherapy of …, 2023 - ncbi.nlm.nih.gov
Background Enzalutamide, a next-generation antiandrogen agent, is approved for the
treatment of metastatic castration-resistant prostate cancer (CRPC). While enzalutamide has …
treatment of metastatic castration-resistant prostate cancer (CRPC). While enzalutamide has …
Combination AZD5363 with enzalutamide significantly delays enzalutamide-resistant prostate cancer in preclinical models
P Toren, S Kim, T Cordonnier, C Crafter, BR Davies… - European urology, 2015 - Elsevier
Abstract The phosphatidylinositol-4, 5-bisphosphate 3-kinase/Akt (PI3K/Akt) pathway is a
key pathway activated in castrate-resistant prostate cancer (CRPC). This preclinical study …
key pathway activated in castrate-resistant prostate cancer (CRPC). This preclinical study …
[HTML][HTML] Targeted cytotoxic analog of luteinizing hormone-releasing hormone (LHRH), AEZS-108 (AN-152), inhibits the growth of DU-145 human castration-resistant …
P Popovics, AV Schally, L Szalontay, NL Block… - Oncotarget, 2014 - ncbi.nlm.nih.gov
Management of castration-resistant prostate cancer (CRPC) is challenging due to lack of
efficacious therapy. Luteinizing hormone-releasing hormone (LHRH) analogs appear to act …
efficacious therapy. Luteinizing hormone-releasing hormone (LHRH) analogs appear to act …
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- combination with enzalutamide antitumor activity
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- prostate cancer xenograft growth
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- prostate cancer therapeutic agents
- prostate cancer therapeutic potential
- dual targeting androgen receptor
- therapeutic potential androgen receptor