Abstract 5149: Nucleostemin is a key factor in maintenance of human glioblastoma-derived cancer stem cells

Author(s):  
Marta L. Izquierdo ◽  
Jon Gil
Cells ◽  
2020 ◽  
Vol 9 (6) ◽  
pp. 1450 ◽  
Author(s):  
Patrick Santos ◽  
Fausto Almeida

Tumor microenvironment (TME) is composed of different cellular populations, such as stromal, immune, endothelial, and cancer stem cells. TME represents a key factor for tumor heterogeneity maintenance, tumor progression, and drug resistance. The transport of molecules via extracellular vesicles emerged as a key messenger in intercellular communication in the TME. Exosomes are small double-layered lipid extracellular vesicles that can carry a variety of molecules, including proteins, lipids, and nucleic acids. Exosomal miRNA released by cancer cells can mediate phenotypical changes in the cells of TME to promote tumor growth and therapy resistance, for example, fibroblast- and macrophages-induced differentiation. Cancer stem cells can transfer and enhance drug resistance in neighboring sensitive cancer cells by releasing exosomal miRNAs that target antiapoptotic and immune-suppressive pathways. Exosomes induce drug resistance by carrying ABC transporters, which export chemotherapeutic agents out of the recipient cells, thereby reducing the drug concentration to suboptimal levels. Exosome biogenesis inhibitors represent a promising adjunct therapeutic approach in cancer therapy to avoid the acquisition of a resistant phenotype. In conclusion, exosomal miRNAs play a crucial role in the TME to confer drug resistance and survivability to tumor cells, and we also highlight the need for further investigations in this promising field.


2009 ◽  
Vol 69 (8) ◽  
pp. 3472-3481 ◽  
Author(s):  
Hiroaki Wakimoto ◽  
Santosh Kesari ◽  
Christopher J. Farrell ◽  
William T. Curry ◽  
Cecile Zaupa ◽  
...  

2015 ◽  
Vol 29 (1) ◽  
pp. 105-109 ◽  
Author(s):  
Francesco Alessandrini ◽  
Ilaria Cristofaro ◽  
Maria Di Bari ◽  
Jacopo Zasso ◽  
Luciano Conti ◽  
...  

2021 ◽  
Vol 22 (17) ◽  
pp. 9280
Author(s):  
Hilal Arnouk ◽  
Gloria Yum ◽  
Dean Shah

Cripto-1 is an essential protein for human development that plays a key role in the early phase of gastrulation in the differentiation of an embryo as well as assists with wound healing processes. Importantly, Cripto-1 induces epithelial to mesenchymal transition to turn fixed epithelial cells into a more mobile mesenchymal phenotype through the downregulation of epithelial adhesion molecules such as E-cadherin, occludins, and claudins, and the upregulation of mesenchymal, mobile proteins, such as N-cadherin, Snail, and Slug. Consequently, Cripto-1’s role in inducing EMT to promote cell motility is beneficial in embryogenesis, but detrimental in the formation, progression and metastasis of malignant tumors. Indeed, Cripto-1 is found to be upregulated in most cancers, such as breast, lung, gastrointestinal, hepatic, renal, cervical, ovarian, prostate, and skin cancers. Through its role in EMT, Cripto-1 can remodel cancer cells to enable them to travel through the extracellular matrix as well as blood and lymphatic vessels to metastasize to different organs. Additionally, Cripto-1 promotes the survival of cancer stem cells, which can lead to relapse in cancer patients.


2008 ◽  
Vol 265 (1) ◽  
pp. 124-134 ◽  
Author(s):  
Shi-cang Yu ◽  
Yi-fang Ping ◽  
Liang Yi ◽  
Zhi-hua Zhou ◽  
Jian-hong Chen ◽  
...  

2015 ◽  
Author(s):  
Soo Jung Ha ◽  
Marisol Herrera-Perez ◽  
Jiri Adamec ◽  
R. Timothy Bentley ◽  
Jenna L. Rickus ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (8) ◽  
pp. e105166 ◽  
Author(s):  
Fortunata Iacopino ◽  
Cristiana Angelucci ◽  
Roberto Piacentini ◽  
Filippo Biamonte ◽  
Annunziato Mangiola ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document