The Synergistic Benefit of Combination Strategies Targeting Tumor Cell Polyamine Homeostasis
Open Access
- 26 July 2024
- journal article
- review article
- Published by MDPI AG in International Journal of Molecular Sciences
- Vol. 25 (15) , 8173
Abstract
Mammalian polyamines, including putrescine, spermidine, and spermine, are positively charged amines that are essential for all living cells including neoplastic cells. An increasing understanding of polyamine metabolism, its molecular functions, and its role in cancer has led to the interest in targeting polyamine metabolism as an anticancer strategy, as the metabolism of polyamines is frequently dysregulated in neoplastic disease. In addition, due to compensatory mechanisms, combination therapies are clinically more promising, as agents can work synergistically to achieve an effect beyond that of each strategy as a single agent. In this article, the nature of polyamines, their association with carcinogenesis, and the potential use of targeting polyamine metabolism in treating and preventing cancer as well as combination therapies are described. The goal is to review the latest strategies for targeting polyamine metabolism, highlighting new avenues for exploiting aberrant polyamine homeostasis for anticancer therapy and the mechanisms behind them.Keywords
Funding Information
- NIH (R01CA235865, R01CA204345, R01HD110500)
- Samuel Waxman Cancer Research Foundation (R01CA235865, R01CA204345, R01HD110500)
- Commonwealth Fund (R01CA235865, R01CA204345, R01HD110500)
- Panbela Therapeutics, Inc. (R01CA235865, R01CA204345, R01HD110500)
This publication has 200 references indexed in Scilit:
- AMXT-1501, a novel polyamine transport inhibitor, synergizes with DFMO in inhibiting neuroblastoma cell proliferation by targeting both ornithine decarboxylase and polyamine transportInternational Journal of Cancer, 2013
- Antizyme and antizyme inhibitor, a regulatory tangoCellular and Molecular Life Sciences, 2009
- In vitro and in vivo effects of the conformationally restricted polyamine analogue CGC-11047 on small cell and non-small cell lung cancer cellsCancer Chemotherapy and Pharmacology, 2008
- Increased spermine oxidase expression in human prostate cancer and prostatic intraepithelial neoplasia tissuesThe Prostate, 2008
- Intestinal tumor and agmatine (decarboxylated arginine)Cancer, 2004
- Core promoter involvement in the induction of rat ornithine decarboxylase by phorbol estersMolecular Carcinogenesis, 2001
- Half-Lives of Ornithine Decarboxylase and S-Adenosylmethionine Decarboxylase Activities during the Cell Cycle of Chinese Hamster Ovary CellsBiochemical and Biophysical Research Communications, 1999
- Growth and biochemical effects of unsymmetrically substituted polyamine analogues in human lung tumor cells 1Cancer Chemotherapy and Pharmacology, 1995
- Regulation of ornithine decarboxylase during cell growth. Changes in the stability and translatability of the mRNA, and in the turnover of the proteinMolecular and Cellular Biochemistry, 1995
- Effects of difluoromethylornithine on proliferation, polyamine content and plating efficiency of cultured human carcinoma cellsCancer Chemotherapy and Pharmacology, 1985