Expanded Potential of the Polyamine Analogue SBP-101 (Diethyl Dihydroxyhomospermine) as a Modulator of Polyamine Metabolism and Cancer Therapeutic.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
18 Jun 2022
Historique:
received: 31 05 2022
revised: 14 06 2022
accepted: 15 06 2022
entrez: 24 6 2022
pubmed: 25 6 2022
medline: 28 6 2022
Statut: epublish

Résumé

Naturally occurring polyamines are absolutely required for cellular growth and proliferation. Many neoplastic cells are reliant on elevated polyamine levels and maintain these levels through dysregulated polyamine metabolism. The modulation of polyamine metabolism is thus a promising avenue for cancer therapeutics and has been attempted with numerous molecules, including enzyme inhibitors and polyamine analogues. SBP-101 (diethyl dihydroxyhomospermine) is a spermine analogue that has shown efficacy in slowing pancreatic tumor progression both in vitro and in vivo; however, the mechanisms underlying these effects remain unclear. We determined the effects of the SBP-101 treatment on a variety of cancer cell types in vitro, including lung, pancreatic, and ovarian. We evaluated the activity of enzymes involved in polyamine metabolism and the effect on intracellular polyamine pools following the SBP-101 treatment. The SBP-101 treatment produced a modest but variable increase in polyamine catabolism; however, a robust downregulation of the activity of the biosynthetic enzyme, ornithine decarboxylase (ODC), was seen across all of the cell types studied and indicates that SBP-101 likely exerts its effect predominately through the downregulation of ODC, with a minor upregulation of catabolism. Our in vitro work indicated that SBP-101 was most toxic in the tested ovarian cell lines. Therefore, we evaluated the efficacy of SBP-101 as a monotherapy in the immunosuppressive VDID8

Identifiants

pubmed: 35743239
pii: ijms23126798
doi: 10.3390/ijms23126798
pmc: PMC9224330
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Polyamines 0
Spermine 2FZ7Y3VOQX
Ornithine Decarboxylase EC 4.1.1.17

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Samuel Waxman Cancer Research Foundation
Organisme : NIH HHS
ID : CA235863
Pays : United States
Organisme : Chan Zuckerberg Initiative (United States)
Organisme : Panbela Therapeutics, Inc.
ID : research contract
Organisme : University of Pennsylvania Orphan Disease Center Million Dollar Bike Ride
ID : MDBR-20-135-SRS
Organisme : NCI NIH HHS
ID : R01 CA204345
Pays : United States
Organisme : NIH HHS
ID : CA204345
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA235863
Pays : United States

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Auteurs

Cassandra E Holbert (CE)

Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD 21231, USA.

Jackson R Foley (JR)

Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD 21231, USA.

Tracy Murray Stewart (T)

Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD 21231, USA.

Robert A Casero (RA)

Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD 21231, USA.

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Classifications MeSH