Inhibition of the Lysophosphatidylinositol Transporter ABCC1 Reduces Prostate Cancer Cell Growth and Sensitizes to Chemotherapy.

ABC transporter ABCC1/MRP1 Docetaxel lysophosphatidylinositol prostate cancer

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
23 Jul 2020
Historique:
received: 06 05 2020
revised: 13 07 2020
accepted: 17 07 2020
entrez: 29 7 2020
pubmed: 29 7 2020
medline: 29 7 2020
Statut: epublish

Résumé

Expression of ATP-binding cassette (ABC) transporters has long been implicated in cancer chemotherapy resistance. Increased expression of the ABCC subfamily transporters has been reported in prostate cancer, especially in androgen-resistant cases. ABCC transporters are known to efflux drugs but, recently, we have demonstrated that they can also have a more direct role in cancer progression. The pharmacological potential of targeting ABCC1, however, remained to be assessed. In this study, we investigated whether the blockade of ABCC1 affects prostate cancer cell proliferation using both in vitro and in vivo models. Our data demonstrate that pharmacological inhibition of ABCC1 reduced prostate cancer cell growth in vitro and potentiated the effects of Docetaxel in vitro and in mouse models of prostate cancer in vivo. Collectively, these data identify ABCC1 as a novel and promising target in prostate cancer therapy.

Identifiants

pubmed: 32718079
pii: cancers12082022
doi: 10.3390/cancers12082022
pmc: PMC7465469
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Prostate Cancer UK
ID : PG12-23
Pays : United Kingdom

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Auteurs

Aikaterini Emmanouilidi (A)

Metabolic Signalling Group, School of Pharmacy and Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, WA 6102, Australia.

Ilaria Casari (I)

Metabolic Signalling Group, School of Pharmacy and Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, WA 6102, Australia.

Begum Gokcen Akkaya (B)

Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK.

Tania Maffucci (T)

Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK.

Luc Furic (L)

Prostate Cancer Translational Research Laboratory, Peter MacCallum Cancer Centre, Melbourne, VI 3000, Australia.
Cancer Program, Biomedicine Discovery Institute and Department of Anatomy and Developmental Biology, Monash University, Clayton, VI 3800, Australia.
Sir Peter MacCallum Department of Oncology, University of Melbourne, Parkville, VI 3010, Australia.

Federica Guffanti (F)

Laboratory of Molecular Pharmacology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156 Milan, Italy.

Massimo Broggini (M)

Laboratory of Molecular Pharmacology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, 20156 Milan, Italy.

Xi Chen (X)

Drug Discovery Research Center, USA Health Mitchell Cancer Institute, Mobile, AL 36604-1405, USA.

Yulia Y Maxuitenko (YY)

Drug Discovery Research Center, USA Health Mitchell Cancer Institute, Mobile, AL 36604-1405, USA.

Adam B Keeton (AB)

Drug Discovery Research Center, USA Health Mitchell Cancer Institute, Mobile, AL 36604-1405, USA.

Gary A Piazza (GA)

Drug Discovery Research Center, USA Health Mitchell Cancer Institute, Mobile, AL 36604-1405, USA.

Kenneth J Linton (KJ)

Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK.

Marco Falasca (M)

Metabolic Signalling Group, School of Pharmacy and Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University, Perth, WA 6102, Australia.
Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London E1 2AT, UK.

Classifications MeSH