Therapeutic implications of cancer stem cells

2004 ◽  
Vol 14 (1) ◽  
pp. 43-47 ◽  
Author(s):  
Muhammad Al-Hajj ◽  
Michael W Becker ◽  
Max Wicha ◽  
Irving Weissman ◽  
Michael F Clarke
2017 ◽  
Vol 14 (2) ◽  
pp. 372-384 ◽  
Author(s):  
Tamara J. Abou-Antoun ◽  
James S. Hale ◽  
Justin D. Lathia ◽  
Stephen M. Dombrowski

Cancers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 4550
Author(s):  
Laura Gramantieri ◽  
Catia Giovannini ◽  
Fabrizia Suzzi ◽  
Ilaria Leoni ◽  
Francesca Fornari

Hepatocellular carcinoma (HCC) is one of the deadliest cancers. HCC is associated with multiple risk factors and is characterized by a marked tumor heterogeneity that makes its molecular classification difficult to apply in the clinics. The lack of circulating biomarkers for the diagnosis, prognosis, and prediction of response to treatments further undermines the possibility of developing personalized therapies. Accumulating evidence affirms the involvement of cancer stem cells (CSCs) in tumor heterogeneity, recurrence, and drug resistance. Owing to the contribution of CSCs to treatment failure, there is an urgent need to develop novel therapeutic strategies targeting, not only the tumor bulk, but also the CSC subpopulation. Clarification of the molecular mechanisms influencing CSC properties, and the identification of their functional roles in tumor progression, may facilitate the discovery of novel CSC-based therapeutic targets to be used alone, or in combination with current anticancer agents, for the treatment of HCC. Here, we review the driving forces behind the regulation of liver CSCs and their therapeutic implications. Additionally, we provide data on their possible exploitation as prognostic and predictive biomarkers in patients with HCC.


2011 ◽  
Vol 7 (2) ◽  
pp. 128-135 ◽  
Author(s):  
Brian J. Wilson ◽  
Tobias Schatton ◽  
Markus H. Frank ◽  
Natasha Y. Frank

2011 ◽  
Vol 9 (1-6) ◽  
pp. 65-99 ◽  
Author(s):  
Thanemozhi G. Natarajan ◽  
Natarajan Ganesan ◽  
Kevin T. FitzGerald

2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
Eunice Yuen-Ting Lau ◽  
Nicole Pui-Yu Ho ◽  
Terence Kin-Wah Lee

Tumor consists of heterogeneous cancer cells including cancer stem cells (CSCs) that can terminally differentiate into tumor bulk. Normal stem cells in normal organs regulate self-renewal within a stem cell niche. Likewise, accumulating evidence has also suggested that CSCs are maintained extrinsically within the tumor microenvironment, which includes both cellular and physical factors. Here, we review the significance of stromal cells, immune cells, extracellular matrix, tumor stiffness, and hypoxia in regulation of CSC plasticity and therapeutic resistance. With a better understanding of how CSC interacts with its niche, we are able to identify potential therapeutic targets for the development of more effective treatments against cancer.


Oncotarget ◽  
2016 ◽  
Vol 8 (10) ◽  
pp. 17301-17312 ◽  
Author(s):  
Xiewan Chen ◽  
Rongxia Liao ◽  
Dezhi Li ◽  
Jianguo Sun

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