Raloxifene Suppresses Tumor Growth and Metastasis in an Orthotopic Model of Castration-Resistant Prostate Cancer.

AR-prostate cancer CRPC anti-cancer agent combination therapy curcumin derivative orthotopic model raloxifene

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
05 Apr 2022
Historique:
received: 15 03 2022
revised: 01 04 2022
accepted: 01 04 2022
entrez: 23 4 2022
pubmed: 24 4 2022
medline: 24 4 2022
Statut: epublish

Résumé

Androgen receptor (AR)-castrate-resistant prostate cancer (CRPC) is an aggressive form of prostate cancer that does not have clinically approved targeted treatment options. To this end, the cytotoxic potential of raloxifene and the synthetic curcumin derivative 2,6-bis (pyridin-4-ylmethylene)-cyclohexanone (RL91) was examined in AR-(PC3 and DU145) cells and AR+ (LnCaP) CRPC cells. The results showed that both raloxifene and RL91 elicited significant cytotoxicity across three cell lines with the lowest EC

Identifiants

pubmed: 35453603
pii: biomedicines10040853
doi: 10.3390/biomedicines10040853
pmc: PMC9033055
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Otago Medical Research Foundation
ID : CT304 and LA325

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Auteurs

Hannah Palmer (H)

Department of Pharmacology and Toxicology, University of Otago, Dunedin 9016, New Zealand.

Mhairi Nimick (M)

Department of Pharmacology and Toxicology, University of Otago, Dunedin 9016, New Zealand.

Aloran Mazumder (A)

Department of Pharmacology and Toxicology, University of Otago, Dunedin 9016, New Zealand.

Sebastien Taurin (S)

Department of Pharmacology and Toxicology, University of Otago, Dunedin 9016, New Zealand.

Zohaib Rana (Z)

Department of Biochemistry, University of Otago, Dunedin 9016, New Zealand.

Rhonda J Rosengren (RJ)

Department of Pharmacology and Toxicology, University of Otago, Dunedin 9016, New Zealand.

Classifications MeSH