Cancer stem cells and mesenchymal stem cells in the hypoxic tumor niche: Two different targets for one only drug

2015 ◽  
Vol 84 (3) ◽  
pp. 227-230
Author(s):  
Francesca Bonafè ◽  
Carlo Guarnieri ◽  
Claudio Muscari
2015 ◽  
Vol 60 (5) ◽  
pp. 763-767 ◽  
Author(s):  
A. G. Konoplyannikov ◽  
A. E. Alekseenskiy ◽  
S. G. Zlotin ◽  
B. B. Smirnov ◽  
S. Sh. Kalsina ◽  
...  

2022 ◽  
Vol 12 (3) ◽  
pp. 597-601
Author(s):  
Haibin Song ◽  
Heng Zhang ◽  
Lei Li

Deriving from bone marrow, the bone marrow mesenchymal stem cells (BMSCs) possess multipolar chemotaxis, proliferation potential, along with the capability to differentiate into various types of cells. Moreover, the hypoxic stimulation can effectively induce BMSCs differentiation. This study intends to explore the impediment of BMSCs on malignant behaviors of lung cancer stem cells under hypoxia. A co-culture system of BMSCs with A549 cells was established and then assigned into normoxia group, hypoxia group (50, 100, and 200 nmol/L) followed by analysis of cell viability by CCK-8 assay and miR-145 expression by qRT-PCR. In addition, A549 cells were grouped into NC group, miR-145-mimics group, and miR-145-inhibitors group followed by analysis of cell invasion and levels of miR-145 and Oct4. Hypoxia group exhibited a reduced cell viability and higher miR-145 expression (146.01±21.23%) compared to normoxia group (P < 0.05). Transfection of miR-145-mimic significantly upregulated miR-145 and decreased cell invasion (7.49±1.43%) compared with miR-145-inhibitors group or NC group (P < 0.05). Meanwhile, Oct4 level in miR-145-mimics group (0.934±2.98) was significantly decreased (P < 0.05). In conclusion, under hypoxia condition, the co-culture with BMSCs can upregulated miR-145 level, effectively reduce the viability of lung cancer stem cells and restrain proliferation capability.


2021 ◽  
Vol 22 ◽  
Author(s):  
Soheila Montazersaheb ◽  
Ezzatollah Fathi ◽  
Ayoub Mamandi ◽  
Raheleh Farahzadi ◽  
Hamid Reza Heidari

: Tumors are made up of different types of cancer cells that contribute to tumor heterogeneity. Among these cells, cancer stem cells (CSCs) have a significant role in the onset of cancer and development. Like other stem cells, CSCs are characterized by the capacity for differentiation and self-renewal. A specific population of CSCs is constituted by mesenchymal stem cells (MSCs) that differentiate into mesoderm-specific cells. The pro-or anti-tumorigenic potential of MSCs on the proliferation and development of tumor cells has been reported as contradictory results. Also, tumor progression is specified by the corresponding tumor cells like the tumor microenvironment. The tumor microenvironment consists of a network of reciprocal cell types such as endothelial cells, immune cells, MSCs, and fibroblasts as well as growth factors, chemokines, and cytokines. In this review, recent findings related to the tumor microenvironment and associated cell populations, homing of MSCs to tumor sites, and interaction of MSCs with tumor cells will be discussed.


2010 ◽  
Vol 316 (20) ◽  
pp. 3417-3424 ◽  
Author(s):  
Yanique Rattigan ◽  
Jing-Mei Hsu ◽  
Pravin J. Mishra ◽  
John Glod ◽  
Debabrata Banerjee

Tumor Biology ◽  
2012 ◽  
Vol 33 (6) ◽  
pp. 1997-2005 ◽  
Author(s):  
Denise Grant Lanza ◽  
Jun Ma ◽  
Ian Guest ◽  
Chang Uk-Lim ◽  
Anna Glinskii ◽  
...  

2020 ◽  
Vol 16 (3) ◽  
pp. 541-556 ◽  
Author(s):  
Zahra naseri ◽  
Reza Kazemi Oskuee ◽  
Mehdi forouzandeh-moghadam ◽  
Mahmoud Reza Jaafari

2011 ◽  
Vol 121 (8) ◽  
pp. 3206-3219 ◽  
Author(s):  
Karen McLean ◽  
Yusong Gong ◽  
Yunjung Choi ◽  
Ning Deng ◽  
Kun Yang ◽  
...  

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