| Literature DB >> 30081228 |
Yue Zhao1, Qiongzhu Dong2, Jiahui Li3, Kaili Zhang2, Jie Qin3, Jiangang Zhao4, Qiye Sun3, Zhefang Wang3, Thomas Wartmann5, Karl Walter Jauch6, Peter J Nelson7, LunXiu Qin2, Christiane Bruns8.
Abstract
A small subpopulation of cells within the bulk of tumors share features with somatic stem cells, in that, they are capable of self-renewal, they differentiate, and are highly resistant to conventional therapy. These cells have been referred to as cancer stem cells (CSCs). Recent reports support the central importance of a cancer stem cell-like niche that appears to help foster the generation and maintenance of CSCs. In response to signals provided by this microenvironment, CSCs express the tumorigenic characteristics that can drive tumor metastasis by the induction of epithelial-mesenchymal-transition (EMT) that in turn fosters the migration and recolonization of the cells as secondary tumors within metastatic niches. We summarize here recent advances in cancer stem cell research including the characterization of their genetic and epigenetic features, metabolic specialities, and crosstalk with aging-associated processes. Potential strategies for targeting CSCs, and their niche, by regulating CSCs plasticity, or therapeutic sensitivity is discussed. Finally, it is hoped that new strategies and related therapeutic approaches as outlined here may help prevent the formation of the metastatic niche, as well as counter tumor progression and metastatic growth.Entities:
Keywords: Cancer stem cells; Metastasis; Microenvironment; Stem cell niche; Therapy resistance
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Year: 2018 PMID: 30081228 DOI: 10.1016/j.semcancer.2018.08.002
Source DB: PubMed Journal: Semin Cancer Biol ISSN: 1044-579X Impact factor: 15.707