Cancer Stem Cells and Autophagy: Present Knowledge and Future Perspectives

Author(s):  
Bakiye Goker Bagca ◽  
Cigir Biray Avci
Cancers ◽  
2019 ◽  
Vol 11 (12) ◽  
pp. 1821 ◽  
Author(s):  
Panagiotis Karakaidos ◽  
John Verigos ◽  
Angeliki Magklara

A new exciting area in cancer research is the study of cancer stem cells (CSCs) and the translational implications for putative epigenetic therapies targeted against them. Accumulating evidence of the effects of epigenetic modulating agents has revealed their dramatic consequences on cellular reprogramming and, particularly, reversing cancer stemness characteristics, such as self-renewal and chemoresistance. Lysine specific demethylase 1 (LSD1/KDM1A) plays a well-established role in the normal hematopoietic and neuronal stem cells. Overexpression of LSD1 has been documented in a variety of cancers, where the enzyme is, usually, associated with the more aggressive types of the disease. Interestingly, recent studies have implicated LSD1 in the regulation of the pool of CSCs in different leukemias and solid tumors. However, the precise mechanisms that LSD1 uses to mediate its effects on cancer stemness are largely unknown. Herein, we review the literature on LSD1’s role in normal and cancer stem cells, highlighting the analogies of its mode of action in the two biological settings. Given its potential as a pharmacological target, we, also, discuss current advances in the design of novel therapeutic regimes in cancer that incorporate LSD1 inhibitors, as well as their future perspectives.


2020 ◽  
Vol 21 (9) ◽  
pp. 3114 ◽  
Author(s):  
Jakub Litak ◽  
Cezary Grochowski ◽  
Joanna Litak ◽  
Ida Osuchowska ◽  
Krzysztof Gosik ◽  
...  

Toll-like-receptor (TLR) family members were detected in the central nervous system (CNS). TLR occurrence was noticed and widely described in glioblastomamultiforme (GBM) cells. After ligand attachment, TLR-4 reorients domains and dimerizes, activates an intracellular cascade, and promotes further cytoplasmatic signaling. There is evidence pointing at a strong relation between TLR-4 signaling and micro ribonucleic acid (miRNA) expression. The TLR-4/miRNA interplay changes typical signaling and encourages them to be a target for modern immunotherapy. TLR-4 agonists initiate signaling and promote programmed death ligand-1 (PD-1L) expression. Most of those molecules are intensively expressed in the GBM microenvironment, resulting in the autocrine induction of regional immunosuppression. Another potential target for immunotreatment is connected with limited TLR-4 signaling that promotes Wnt/DKK-3/claudine-5 signaling, resulting in a limitation of GBM invasiveness. Interestingly, TLR-4 expression results in bordering proliferative trends in cancer stem cells (CSC) and GBM. All of these potential targets could bring new hope for patients suffering from this incurable disease. Clinical trials concerning TLR-4 signaling inhibition/promotion in many cancers are recruiting patients. There is still a lot to do in the field of GBM immunotherapy.


2019 ◽  
Vol 95 (7) ◽  
pp. 900-911 ◽  
Author(s):  
Claudia Peitzsch ◽  
Ina Kurth ◽  
Nadja Ebert ◽  
Anna Dubrovska ◽  
Michael Baumann

2019 ◽  
Vol 11 (7) ◽  
pp. 398-420 ◽  
Author(s):  
Fang-Yu Du ◽  
Qi-Fan Zhou ◽  
Wen-Jiao Sun ◽  
Guo-Liang Chen

Oncotarget ◽  
2021 ◽  
Vol 12 (3) ◽  
pp. 230-250
Author(s):  
Beatrice Aramini ◽  
Valentina Masciale ◽  
Giulia Grisendi ◽  
Federico Banchelli ◽  
Roberto D’Amico ◽  
...  

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