scholarly journals Analysis of in vitro activity of high dilutions of Euphorbia tirucalli L. in human melanoma cells

2021 ◽  
Vol 10 (36) ◽  
pp. 183-193
Author(s):  
Renata Macedo dos Reis Januário Da Silva ◽  
Dulcinéia Furtado Teixeira ◽  
André Luiz Franco Sampaio ◽  
Teresa Cristina Andrade Leitao Aguiar

Aveloz (firestick cactus; Euphorbia tirucalli L.) belongs to Euphorbiaceae family, characterized by the production of a toxic latex that has corrosive effects on the skin and mucous membranes. Continual topic use of the latex is recommended by popular medicine to treat warts, and epitheliomas. To validate this indication, ultra diluted latex and homeopathic medicine Euphorbia tirucalli were tested in vitro on the proliferation of melanoma cells. Ultra diluted latex was prepared in homeopathic dilutions 5cH, 15cH and 30cH by dilution and agitation (trituration for solid and sucussion for liquid phases) using 70º GL (Gay Lussac) ethylic alcohol (70º GL EtOH 70ºGL) as inert medium according to the guidelines in Farmacopéia Homeopática Brasileira (FHB). Homeopathic medicine Euphorbia tirucalli was prepared from mother-tincture according to the centesimal Hahnemannian method. Solutions 0.5% and 5% of 70ºGL EtOH were succussed and used as control. Human melanoma cells were cultured, treated and monitored by method MTT for 24 to 72 hours. It was observed that 0.5% 70ºGL EtOH solution had little or no effect on the proliferation of melanoma cells (5.1% maximal inhibition in dilution 30cH). Positive correlation was observed in most groups between inhibition of proliferation and diluted preparations, maximal increase (9%) was seen in with 5% latex. Moreover, mother-tincture proved to be more active than latex; treatment with 0.5% solution of latex 30cH exhibited 19.7% inhibition, whereas treatment with 0.5% solution of Euphorbia tirucalli 30cH exhibited 32.1% inhibition of cell proliferation (p

2021 ◽  
Vol 70 (3) ◽  
Author(s):  
Bernadetta Bilska ◽  
Fiona Schedel ◽  
Anna Piotrowska ◽  
Joanna Stefan ◽  
Michal Zmijewski ◽  
...  

1991 ◽  
Vol 1 (2) ◽  
pp. 91-96 ◽  
Author(s):  
Ch. C. Zouboulis ◽  
C. Garbe ◽  
K. Krasagakis ◽  
S. Krüger ◽  
C. E. Orfanos

1998 ◽  
Vol 8 (4) ◽  
pp. 323-328 ◽  
Author(s):  
O Franzese ◽  
A Comandini ◽  
E Cannav?? ◽  
R Pepponi ◽  
S Falcinelli ◽  
...  

2001 ◽  
Vol 11 (1) ◽  
pp. 91-102 ◽  
Author(s):  
Anna Poma ◽  
Patrizia Cesare ◽  
Giordana Marcozzi ◽  
Laura Spanò

2016 ◽  
Vol 480 (4) ◽  
pp. 515-521 ◽  
Author(s):  
Lezi Chen ◽  
Quan Chen ◽  
Guosan Deng ◽  
Shifeng Kuang ◽  
Jihong Lian ◽  
...  

1996 ◽  
Vol 135 (6) ◽  
pp. 1889-1898 ◽  
Author(s):  
D Schadendorf ◽  
M A Kern ◽  
M Artuc ◽  
H L Pahl ◽  
T Rosenbach ◽  
...  

Human malignant melanoma is notoriously resistant to pharmacological modulation. We describe here for the first time that the synthetic retinoid CD437 has a strong dose-dependent antiproliferative effect on human melanoma cells (IC50: 5 x 10(-6) M) via the induction of programmed cell death, as judged by analysis of cell morphology, electron microscopical features, and DNA fragmentation. Programmed cell death was preceded by a strong activation of the AP-1 complex in CD437-treated cells as demonstrated by gel retardation and chloramphenicol transferase (CAT) assays. Northern blot analysis showed a time-dependent increase in the expression of c-fos and c-jun encoding components of AP-1, whereas bcl-2 and p53 mRNA levels remained constant. CD437 also exhibited a strong growth inhibitory effect on MeWo melanoma cells in a xenograft model. In tissue sections of CD437-treated MeWo tumors from these animals, apoptotic melanoma cells and c-fos overexpressing cells were colocalized by TdT-mediated deoxyuridine triphosphate-digoxigenin nick end labeling (TUNEL) staining and in situ hybridization. Taken together, this report identifies CD437 as a retinoid that activates and upregulates the transcription factor AP-1, leading eventually to programmed cell death of exposed human melanoma cells in vitro and in vivo. Further studies are needed to evaluate whether synthetic retinoids such as CD437 represent a new class of retinoids, which may open up new ways to a more effective therapy of malignant melanoma.


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