scholarly journals Potential antiproliferative effect of isoxazolo- and thiazolo coumarin derivatives on breast cancer mediated bone and lung metastases

2015 ◽  
Vol 65 (1) ◽  
pp. 53-63 ◽  
Author(s):  
Lulzime Ballazhi ◽  
Emil Popovski ◽  
Ahmed Jashari ◽  
Faik Imeri ◽  
Ibrahim Ibrahimi ◽  
...  

Abstract The study highlights the current progress in the development of coumarin scaffolds for drug discovery as novel anticancer agents in metastatic breast cancer. Eight compounds, combining the coumarin core and five membered heterocycles (isoxazoles and thiazoles) in hydrazinyldiene- -chroman-2,4-diones, were characterized in terms of a potential antiproliferative effect on bone (SCP1833) and lung (SCP4175) metastatic breast cancer cell lines using the 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide assay. Cell viability was evaluated after 48 and 72 h of treatment and the 50 % inhibitory concentrations were determined. The results demonstrated dose- and time-dependent activity, with the most potent molecules having a thiazole moiety, without or with additional methyl group(s) attached to the carbon(s) at position(s) 5 and/or 4 in the thiazole ring. These molecules possessed significantly higher potency against both test cell lines compared to 4-hydroxycoumarin

2007 ◽  
Vol 120 (6) ◽  
pp. 1179-1191 ◽  
Author(s):  
Behjatolah Monzavi-Karbassi ◽  
J. Steven Stanley ◽  
Leah Hennings ◽  
Fariba Jousheghany ◽  
Cecile Artaud ◽  
...  

Oncotarget ◽  
2017 ◽  
Vol 8 (12) ◽  
pp. 20266-20287 ◽  
Author(s):  
Paul T. Winnard ◽  
Chi Zhang ◽  
Farhad Vesuna ◽  
Jeon Woong Kang ◽  
Jonah Garry ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Ke Liu ◽  
Patrick A. Newbury ◽  
Benjamin S. Glicksberg ◽  
William Z. D. Zeng ◽  
Shreya Paithankar ◽  
...  

AbstractCell lines are widely-used models to study metastatic cancer although the extent to which they recapitulate the disease in patients remains unknown. The recent accumulation of genomic data provides an unprecedented opportunity to evaluate the utility of them for metastatic cancer research. Here, we reveal substantial genomic differences between breast cancer cell lines and metastatic breast cancer patient samples. We also identify cell lines that more closely resemble the different subtypes of metastatic breast cancer seen in the clinic and show that surprisingly, MDA-MB-231 cells bear little genomic similarities to basal-like metastatic breast cancer patient samples. Further comparison suggests that organoids more closely resemble the transcriptome of metastatic breast cancer samples compared to cell lines. Our work provides a guide for cell line selection in the context of breast cancer metastasis and highlights the potential of organoids in these studies.


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