Polyamines in cancer: integrating organismal metabolism and antitumour immunity

被引:222
作者
Holbert, Cassandra E. [1 ]
Cullen, Michael T. [2 ]
Casero, Robert A., Jr. [1 ]
Stewart, Tracy Murray [1 ]
机构
[1] Johns Hopkins Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
[2] Panbela Therapeut Inc, Waconia, MN USA
基金
美国国家卫生研究院;
关键词
ORNITHINE-DECARBOXYLASE ACTIVITY; CELL LUNG-CANCER; ALPHA-DIFLUOROMETHYLORNITHINE; SUPPRESSOR-CELLS; HUMAN COLON; GASTROINTESTINAL-TRACT; EXOGENOUS POLYAMINES; TRANSPORT INHIBITORS; EXPRESSION PATTERNS; HELICOBACTER-PYLORI;
D O I
10.1038/s41568-022-00473-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The natural mammalian polyamines putrescine, spermidine and spermine are essential for both normal and neoplastic cell function and replication. Dysregulation of metabolism of polyamines and their requirements is common in many cancers. Both clinical and experimental depletion of polyamines have demonstrated their metabolism to be a rational target for therapy; however, the mechanisms through which polyamines can establish a tumour-permissive microenvironment are only now emerging. Recent data indicate that polyamines can play a major role in regulating the antitumour immune response, thus likely contributing to the existence of immunologically 'cold' tumours that do not respond to immune checkpoint blockade. Additionally, the interplay between the microbiota and associated tissues creates a tumour microenvironment in which polyamine metabolism, content and function can all be dramatically altered on the basis of microbiota composition, dietary polyamine availability and tissue response to its surrounding microenvironment. The goal of this Perspective is to introduce the reader to the many ways in which polyamines, polyamine metabolism, the microbiota and the diet interconnect to establish a tumour microenvironment that facilitates the initiation and progression of cancer. It also details ways in which polyamine metabolism and function can be successfully targeted for therapeutic benefit, including specifically enhancing the antitumour immune response. This Perspective discusses how polyamines, polyamine metabolism, the microbiota and the diet interconnect to establish a tumour microenvironment that facilitates the initiation and progression of cancer. It also details ways in which polyamine metabolism and function can be targeted for therapeutic benefit, including specifically enhancing the antitumour immune response.
引用
收藏
页码:467 / 480
页数:14
相关论文
共 194 条
[1]   Polyamines and membrane transporters [J].
Abdulhussein, Ahmed A. ;
Wallace, Heather M. .
AMINO ACIDS, 2014, 46 (03) :655-660
[2]   The Molecular Taxonomy of Primary Prostate Cancer [J].
Abeshouse, Adam ;
Ahn, Jaeil ;
Akbani, Rehan ;
Ally, Adrian ;
Amin, Samirkumar ;
Andry, Christopher D. ;
Annala, Matti ;
Aprikian, Armen ;
Armenia, Joshua ;
Arora, Arshi ;
Auman, J. Todd ;
Balasundaram, Miruna ;
Balu, Saianand ;
Barbieri, Christopher E. ;
Bauer, Thomas ;
Benz, Christopher C. ;
Bergeron, Alain ;
Beroukhim, Rameen ;
Berrios, Mario ;
Bivol, Adrian ;
Bodenheimer, Tom ;
Boice, Lori ;
Bootwalla, Moiz S. ;
dos Reis, Rodolfo Borges ;
Boutros, Paul C. ;
Bowen, Jay ;
Bowlby, Reanne ;
Boyd, Jeffrey ;
Bradley, Robert K. ;
Breggia, Anne ;
Brimo, Fadi ;
Bristow, Christopher A. ;
Brooks, Denise ;
Broom, Bradley M. ;
Bryce, Alan H. ;
Bubley, Glenn ;
Burks, Eric ;
Butterfield, Yaron S. N. ;
Button, Michael ;
Canes, David ;
Carlotti, Carlos G. ;
Carlsen, Rebecca ;
Carmel, Michel ;
Carroll, Peter R. ;
Carter, Scott L. ;
Cartun, Richard ;
Carver, Brett S. ;
Chan, June M. ;
Chang, Matthew T. ;
Chen, Yu .
CELL, 2015, 163 (04) :1011-1025
[3]   Tumor Hypoxia Regulates Immune Escape/Invasion: Influence on Angiogenesis and Potential Impact of Hypoxic Biomarkers on Cancer Therapies [J].
Abou Khouzam, Raefa ;
Brodaczewska, Klaudia ;
Filipiak, Aleksandra ;
Zeinelabdin, Nagwa Ahmed ;
Buart, Stephanie ;
Szczylik, Cezary ;
Kieda, Claudine ;
Chouaib, Salem .
FRONTIERS IN IMMUNOLOGY, 2021, 11
[4]   Harnessing the polyamine transport system to treat BRAF inhibitor-resistant melanoma [J].
Alexander, Eric T. ;
El Naggar, Olivia ;
Fahey, Erin ;
Mariner, Kelsey ;
Donnelly, Julia ;
Wolfgang, Katelyn ;
Phanstiel, Otto ;
Gilmour, Susan K. .
CANCER BIOLOGY & THERAPY, 2021, 22 (03) :225-237
[5]   Polyamine Blocking Therapy Decreases Survival of Tumor-Infiltrating Immunosuppressive Myeloid Cells and Enhances the Antitumor Efficacy of PD-1 Blockade [J].
Alexander, Eric T. ;
Mariner, Kelsey ;
Donnelly, Julia ;
Phanstiel, Otto ;
Gilmour, Susan K. .
MOLECULAR CANCER THERAPEUTICS, 2020, 19 (10) :2012-2022
[6]   A novel polyamine blockade therapy activates an anti-tumor immune response [J].
Alexander, Eric T. ;
Minton, Allyson ;
Peters, Molly C. ;
Phanstiel, Otto ;
Gilmour, Susan K. .
ONCOTARGET, 2017, 8 (48) :84140-84152
[7]   Oil for the cancer engine: The cross-talk between oncogenic signaling and polyamine metabolism [J].
Arruabarrena-Aristorena, Amaia ;
Zabala-Letona, Amaia ;
Carracedo, Arkaitz .
SCIENCE ADVANCES, 2018, 4 (01)
[8]  
Bacchi Cyrus J, 2009, Interdiscip Perspect Infect Dis, V2009, P195040, DOI 10.1155/2009/195040
[9]   Polyamine synthesis as a target of MYC oncogenes [J].
Bachmann, Andre S. ;
Geerts, Dirk .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (48) :18757-18769
[10]   INTERACTION OF OXIDIZED POLYAMINES WITH DNA .5. INHIBITION OF NUCLEIC ACID SYNTHESIS [J].
BACHRACH, U ;
PERSKY, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 179 (02) :484-&