Natural Products and Small Molecules Targeting Cellular Ceramide Metabolism to Enhance Apoptosis in Cancer Cells

Author:

Afrin Farjana1,Mateen Sameena1,Oman Jordan1,Lai James C. K.1,Barrott Jared J.2,Pashikanti Srinath1

Affiliation:

1. Biomedical and Pharmaceutical Sciences, Kasiska Division of Health Sciences, College of Pharmacy, Idaho State University, Pocatello, ID 83209, USA

2. Cell Biology and Physiology, College of Life Sciences, Brigham Young University, Provo, UT 84602, USA

Abstract

Molecular targeting strategies have been used for years in order to control cancer progression and are often based on targeting various enzymes involved in metabolic pathways. Keeping this in mind, it is essential to determine the role of each enzyme in a particular metabolic pathway. In this review, we provide in-depth information on various enzymes such as ceramidase, sphingosine kinase, sphingomyelin synthase, dihydroceramide desaturase, and ceramide synthase which are associated with various types of cancers. We also discuss the physicochemical properties of well-studied inhibitors with natural product origins and their related structures in terms of these enzymes. Targeting ceramide metabolism exhibited promising mono- and combination therapies at preclinical stages in preventing cancer progression and cemented the significance of sphingolipid metabolism in cancer treatments. Targeting ceramide-metabolizing enzymes will help medicinal chemists design potent and selective small molecules for treating cancer progression at various levels.

Funder

Biomedical and Pharmaceutical Sciences, College of Pharmacy, Idaho State University

National Science Foundation (NSF) MRI

American Association of Colleges of Pharmacy NIA

Office of Research—ISU

Pardee Foundation

Institute for Modeling Collaboration and Innovation, University of Idaho

National Institute of General Medical Sciences

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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