Schweinfurthin natural products induce regression of murine melanoma and pair with anti-PD-1 therapy to facilitate durable tumor immunity.

PD-1 Schweinfurthin immunotherapy melanoma mice

Journal

Oncoimmunology
ISSN: 2162-4011
Titre abrégé: Oncoimmunology
Pays: United States
ID NLM: 101570526

Informations de publication

Date de publication:
Historique:
received: 24 07 2018
revised: 09 10 2018
accepted: 10 10 2018
entrez: 5 2 2019
pubmed: 5 2 2019
medline: 5 2 2019
Statut: epublish

Résumé

Metastatic melanoma is a significant clinical problem with a 5-year survival rate of only 15-20%. Recent approval of new immunotherapies and targeted inhibitors have provided much needed options for these patients, in some cases promoting dramatic disease regressions. In particular, antibody-based therapies that block the PD-1/PD-L1 checkpoint inhibitory pathway have achieved an increased overall response rate in metastatic melanoma, yet durable response rates are reported only around 15%. To improve the overall and durable response rates for advanced-stage melanoma, combined targeted and immune-based therapies are under investigation. Here, we investigated how the natural products called schweinfurthins, which have selective anti-proliferative activity against many cancer types, impact anti-(α)PD-1-mediated immunotherapy of murine melanomas. Two different compounds efficiently reduced the growth of human and murine melanoma cells

Identifiants

pubmed: 30713799
doi: 10.1080/2162402X.2018.1539614
pii: 1539614
pmc: PMC6343772
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Pagination

e1539614

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Auteurs

Kathleen M Kokolus (KM)

Department of Microbiology & Immunology, Penn State College of Medicine, Hershey, PA, USA.

Jeremy S Haley (JS)

Department of Microbiology & Immunology, Penn State College of Medicine, Hershey, PA, USA.

Emily J Koubek (EJ)

Department of Pharmacology, Penn State College of Medicine, Hershey, PA, USA.
Department of Medicine, Penn State College of Medicine, Hershey, PA, USA.

Raghavendra Gowda (R)

Department of Pharmacology, Penn State College of Medicine, Hershey, PA, USA.

Saketh S Dinavahi (SS)

Department of Pharmacology, Penn State College of Medicine, Hershey, PA, USA.

Arati Sharma (A)

Department of Pharmacology, Penn State College of Medicine, Hershey, PA, USA.
Penn State Cancer Institute, Hershey, PA, USA.

David F Claxton (DF)

Department of Medicine, Penn State College of Medicine, Hershey, PA, USA.
Penn State Cancer Institute, Hershey, PA, USA.

Klaus F Helm (KF)

Department of Pathology, Penn State College of Medicine, Hershey, PA, USA.
Department of Dermatology, Penn State College of Medicine, Hershey, PA, USA.

Joseph J Drabick (JJ)

Department of Medicine, Penn State College of Medicine, Hershey, PA, USA.
Department of Pathology, Penn State College of Medicine, Hershey, PA, USA.
Penn State Melanoma and Skin Cancer Center, Hershey, PA, USA.

Gavin P Robertson (GP)

Department of Pharmacology, Penn State College of Medicine, Hershey, PA, USA.
Penn State Cancer Institute, Hershey, PA, USA.
Penn State Melanoma and Skin Cancer Center, Hershey, PA, USA.

Jeffrey D Neighbors (JD)

Department of Pharmacology, Penn State College of Medicine, Hershey, PA, USA.
Department of Medicine, Penn State College of Medicine, Hershey, PA, USA.
Penn State Cancer Institute, Hershey, PA, USA.

Raymond J Hohl (RJ)

Department of Pharmacology, Penn State College of Medicine, Hershey, PA, USA.
Department of Medicine, Penn State College of Medicine, Hershey, PA, USA.
Penn State Cancer Institute, Hershey, PA, USA.

Todd D Schell (TD)

Department of Microbiology & Immunology, Penn State College of Medicine, Hershey, PA, USA.
Penn State Cancer Institute, Hershey, PA, USA.
Penn State Melanoma and Skin Cancer Center, Hershey, PA, USA.

Classifications MeSH