scholarly journals Antiproliferative Activity of Selected Triterpene Acids from Rosemary on Metastatic Melanoma Cell Line WM-266-4

2021 ◽  
Vol 9 (B) ◽  
pp. 515-521
Author(s):  
Suzana Isaković-Vidović ◽  
Barbara Dariš ◽  
Željko Knez ◽  
Kristina Vidović ◽  
Dejan Oprić ◽  
...  

BACKGROUND: Natural products and their derivatives, particularly secondary metabolites, have been recognized for many years as an important source of therapeutic agents. In this context, pentacyclic triterpene acids including betulinic acid (BA), oleanolic acid (OA), and ursolic acid (UA) are highly valuable triterpenic acids because of their wide range of biological activities. AIM: Therefore, the aim of our study was to investigate any potential effect of BA, UA, and OA on human melanoma WM-266-4 cells’ proliferation activity. METHODS: BA, UA, and OA have been prepared in dimethyl sulfoxide in concentration range from 0.002 to 200 μM separately or in selected combination (UA+OA ratio 1:1 or 3.5:1), while cells in cell culture medium served as controls. The rapid colorimetric MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay was used to measure proliferation activity of the metastatic melanoma cell line WM-266-4 after being exposed to selected concentrations of BA, UA, OA, or UA+OA and during different time periods. Student’s t-test was used for single statistical comparisons. Data were analyzed using IBM SPSS 25.0 (IBM Corp., Armonk, NY). To account for multiple comparisons bias, p < 0.001 was considered statistically significant. RESULTS: Our results showed decreased cell proliferation activity after 4 h of incubation of WM-266-4 cells with BA, UA, OA, and UA+OA. The highest inhibitory effect was noted when cells were incubated with selected triterpenic acids and both combinations of UA+OA during the incubation period of 48 h. When compared to control cells, concentration of 2 μM was the lowest concentration of BA that showed a significant decrease of the cells’ proliferation activity regardless the incubation period (4 h, 24 h, and 48 h) (p < 0.001). CONCLUSION: Our encouraging results could be a good starting point for further studies on possible use of BA, UA, and OA in prevention and treatment of metastatic melanoma.

2015 ◽  
Vol 39 (4) ◽  
pp. 508-514
Author(s):  
Xiuli Yi ◽  
Guannan Zhu ◽  
Yan Li ◽  
Ying Liu ◽  
Qi Luan ◽  
...  

Author(s):  
Tanja Prunk Zdravković ◽  
Bogdan Zdravković ◽  
Marko Zdravković ◽  
Barbara Dariš ◽  
Mojca Lunder ◽  
...  

2011 ◽  
Vol 10 (12) ◽  
pp. 5444-5453 ◽  
Author(s):  
Maddalena Di Sanzo ◽  
Marco Gaspari ◽  
Roberta Misaggi ◽  
Francesco Romeo ◽  
Lucia Falbo ◽  
...  

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Parvathi Haridas ◽  
Jacqui A. McGovern ◽  
Abhishek S. Kashyap ◽  
D. L. Sean McElwain ◽  
Matthew J. Simpson

2013 ◽  
Vol 50 (1) ◽  
pp. 56-65 ◽  
Author(s):  
Monika H. Seltenhammer ◽  
Elisabeth Sundström ◽  
Claudia Meisslitzer-Ruppitsch ◽  
Petra Cejka ◽  
Jedrzej Kosiuk ◽  
...  

2008 ◽  
Vol 26 (15_suppl) ◽  
pp. 20026-20026
Author(s):  
J. Nesselhut ◽  
D. Marx ◽  
R. Y. Chang ◽  
C. Matthes ◽  
D. Lorenzen ◽  
...  

2019 ◽  
Vol 19 (1) ◽  
pp. 60-66
Author(s):  
Tanja Prunk Zdravković ◽  
Bogdan Zdravković ◽  
Mojca Lunder ◽  
Polonca Ferk

Titanium dioxide (TiO2) is widely used as an inorganic UV-filter in cosmetic products; however, it has been classified as possibly carcinogenic to humans. While numerous studies demonstrated cytotoxic and genotoxic effects of nano-sized TiO2 in different cell lines, including human skin cells, studies investigating the effects of micro-TiO2 on human keratinocytes and melanocytes, in healthy and cancer cells, are scarce. Adenosine triphosphate (ATP) binding cassette subfamily B member 5 (ABCB5) is a plasma membrane protein known for its role in the tumorigenicity, progression, and recurrence of melanoma. Here, we investigated the effect of micro-TiO2 (average particle size ≤5 µm) on the metabolic activity, cytotoxicity and ABCB5 mRNA expression in metastatic melanoma cells. Metastatic melanoma cell line WM-266-4 was treated with different concentrations of micro-TiO2 for different incubation times to obtain dose- and time-dependent responses. Untreated WM-266-4 cells, cultured under the same conditions, were used as control. The cell metabolic activity was determined by MTT assay. Cytotoxicity of micro-TiO2 was analyzed by lactate dehydrogenase (LDH) cytotoxicity assay. The ABCB5 mRNA expression in melanoma cells was analyzed using quantitative reverse transcription polymerase chain reaction (RT-qPCR). After 120 hours of exposure to micro-TiO2 the metabolic activity of melanoma cells decreased, especially at the two highest micro-TiO2 concentrations. Comparably, the cytotoxicity of micro-TiO2 on melanoma cells increased after 48 and 120 hours of exposure, in a time-dependent manner. The ABCB5 mRNA expression in micro-TiO2-treated melanoma cells also decreased significantly after 24 and 48 hours, in a time-dependent manner. Overall, our results suggest inhibitory effects of micro-TiO2 on the metabolic activity and ABCB5 mRNA expression in metastatic melanoma cells, indicating its potential use as an anticancer agent.


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