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Emerging role of lipid metabolism alterations in Cancer stem cells

BACKGROUND: Cancer stem cells (CSCs) or tumor-initiating cells (TICs) represent a small population of cancer cells with self-renewal and tumor-initiating properties. Unlike the bulk of tumor cells, CSCs or TICs are refractory to traditional therapy and are responsible for relapse or disease recurren...

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Autores principales: Yi, Mei, Li, Junjun, Chen, Shengnan, Cai, Jing, Ban, Yuanyuan, Peng, Qian, Zhou, Ying, Zeng, Zhaoyang, Peng, Shuping, Li, Xiaoling, Xiong, Wei, Li, Guiyuan, Xiang, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003041/
https://www.ncbi.nlm.nih.gov/pubmed/29907133
http://dx.doi.org/10.1186/s13046-018-0784-5
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author Yi, Mei
Li, Junjun
Chen, Shengnan
Cai, Jing
Ban, Yuanyuan
Peng, Qian
Zhou, Ying
Zeng, Zhaoyang
Peng, Shuping
Li, Xiaoling
Xiong, Wei
Li, Guiyuan
Xiang, Bo
author_facet Yi, Mei
Li, Junjun
Chen, Shengnan
Cai, Jing
Ban, Yuanyuan
Peng, Qian
Zhou, Ying
Zeng, Zhaoyang
Peng, Shuping
Li, Xiaoling
Xiong, Wei
Li, Guiyuan
Xiang, Bo
author_sort Yi, Mei
collection PubMed
description BACKGROUND: Cancer stem cells (CSCs) or tumor-initiating cells (TICs) represent a small population of cancer cells with self-renewal and tumor-initiating properties. Unlike the bulk of tumor cells, CSCs or TICs are refractory to traditional therapy and are responsible for relapse or disease recurrence in cancer patients. Stem cells have distinct metabolic properties compared to differentiated cells, and metabolic rewiring contributes to self-renewal and stemness maintenance in CSCs. MAIN BODY: Recent advances in metabolomic detection, particularly in hyperspectral-stimulated raman scattering microscopy, have expanded our knowledge of the contribution of lipid metabolism to the generation and maintenance of CSCs. Alterations in lipid uptake, de novo lipogenesis, lipid droplets, lipid desaturation, and fatty acid oxidation are all clearly implicated in CSCs regulation. Alterations on lipid metabolism not only satisfies the energy demands and biomass production of CSCs, but also contributes to the activation of several important oncogenic signaling pathways, including Wnt/β-catenin and Hippo/YAP signaling. In this review, we summarize the current progress in this attractive field and describe some recent therapeutic agents specifically targeting CSCs based on their modulation of lipid metabolism. CONCLUSION: Increased reliance on lipid metabolism makes it a promising therapeutic strategy to eliminate CSCs. Targeting key players of fatty acids metabolism shows promising to anti-CSCs and tumor prevention effects.
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spelling pubmed-60030412018-07-06 Emerging role of lipid metabolism alterations in Cancer stem cells Yi, Mei Li, Junjun Chen, Shengnan Cai, Jing Ban, Yuanyuan Peng, Qian Zhou, Ying Zeng, Zhaoyang Peng, Shuping Li, Xiaoling Xiong, Wei Li, Guiyuan Xiang, Bo J Exp Clin Cancer Res Review BACKGROUND: Cancer stem cells (CSCs) or tumor-initiating cells (TICs) represent a small population of cancer cells with self-renewal and tumor-initiating properties. Unlike the bulk of tumor cells, CSCs or TICs are refractory to traditional therapy and are responsible for relapse or disease recurrence in cancer patients. Stem cells have distinct metabolic properties compared to differentiated cells, and metabolic rewiring contributes to self-renewal and stemness maintenance in CSCs. MAIN BODY: Recent advances in metabolomic detection, particularly in hyperspectral-stimulated raman scattering microscopy, have expanded our knowledge of the contribution of lipid metabolism to the generation and maintenance of CSCs. Alterations in lipid uptake, de novo lipogenesis, lipid droplets, lipid desaturation, and fatty acid oxidation are all clearly implicated in CSCs regulation. Alterations on lipid metabolism not only satisfies the energy demands and biomass production of CSCs, but also contributes to the activation of several important oncogenic signaling pathways, including Wnt/β-catenin and Hippo/YAP signaling. In this review, we summarize the current progress in this attractive field and describe some recent therapeutic agents specifically targeting CSCs based on their modulation of lipid metabolism. CONCLUSION: Increased reliance on lipid metabolism makes it a promising therapeutic strategy to eliminate CSCs. Targeting key players of fatty acids metabolism shows promising to anti-CSCs and tumor prevention effects. BioMed Central 2018-06-15 /pmc/articles/PMC6003041/ /pubmed/29907133 http://dx.doi.org/10.1186/s13046-018-0784-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Yi, Mei
Li, Junjun
Chen, Shengnan
Cai, Jing
Ban, Yuanyuan
Peng, Qian
Zhou, Ying
Zeng, Zhaoyang
Peng, Shuping
Li, Xiaoling
Xiong, Wei
Li, Guiyuan
Xiang, Bo
Emerging role of lipid metabolism alterations in Cancer stem cells
title Emerging role of lipid metabolism alterations in Cancer stem cells
title_full Emerging role of lipid metabolism alterations in Cancer stem cells
title_fullStr Emerging role of lipid metabolism alterations in Cancer stem cells
title_full_unstemmed Emerging role of lipid metabolism alterations in Cancer stem cells
title_short Emerging role of lipid metabolism alterations in Cancer stem cells
title_sort emerging role of lipid metabolism alterations in cancer stem cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003041/
https://www.ncbi.nlm.nih.gov/pubmed/29907133
http://dx.doi.org/10.1186/s13046-018-0784-5
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