The Effect of Marijuana Smoke Exposure on Murine Sarcoma 180 Survival in Fisher Rats

1989 ◽  
Vol 11 (2-3) ◽  
pp. 211-222 ◽  
Author(s):  
E. Sue Watson
RSC Advances ◽  
2015 ◽  
Vol 5 (70) ◽  
pp. 56549-56559 ◽  
Author(s):  
Samarjit Jana ◽  
Kartick Patra ◽  
Gopeswar Mukherjee ◽  
Shamee Bhattacharjee ◽  
Deba Prasad Mandal

Coupling anethole with cyclophosphamide reduces side effect of the latter and enhances apoptosis–necrosis ratio in murine s-180 tumor model.


Author(s):  
Helber A. Negreiros ◽  
Kariely G. de Moura ◽  
Maria L.L.B. do Nascimento ◽  
Débora C.N. Rodrigues ◽  
Paulo M.P. Ferreira ◽  
...  

Background: Alpha-terpineol is a monoterpene alcohol with anti-tumor activity against different tumor cell lines (lung, breast, leukemias and colorectal) through blockage of NF-kB expression, which play an important role in tumor cells growth. Objective: Evaluate the antitumor activity of alpha-terpineol in murine Sarcoma 180 cell line Methods: For the tests, different cytotoxic and genotoxic assays were used, including Trypan blue, cytokinesis-blocked micronucleus assay, comet assay, agarose gel DNA fragmentation, flow cytometry and cell viability using fluorescence. Ascitic fluid cells from sarcoma 180 were obtained from Mus musculus peritoneal cavity and Alpha-terpineol was tested at 100, 250 and 500 μg/mL. Doxorubicin and Cisplatin were used as positive controls. Results: Cytotoxic effects of alpha-terpineol were found in all concentrations tested, reducing cell viability in 50.9; 38.53; 30.82% at 100, 250 and 500 μg/mL, respectively. Alpha-terpineol induced genotoxic effects due to DNA fragmentation (increased frequency and index of damage), and was clastogenic by increased micronuclei formation, nucleoplasmic bridges and nuclear buds. DNA fragmentation and increased cell death indicated that alpha-terpineol can cause early, late, and necrotic apoptosis. Conclusion: Our data indicate that alpha-terpineol has antitumor activity revealed by cytogenetic mechanisms and / or loss of cell membrane integrity.


2010 ◽  
Vol 35 (3) ◽  
pp. 371-378 ◽  
Author(s):  
Aliny Pereira de Lima ◽  
Flavia de Castro Pereira ◽  
Cesar Augusto Sam Tiago Vilanova-Costa ◽  
Alessandra de Santana Braga Barbosa Ribeiro ◽  
Luiz Alfredo Pavanin ◽  
...  

Author(s):  
S. K. Aggarwal ◽  
P. McAllister ◽  
R. W. Wagner ◽  
B. Rosenberg

Uranyl acetate has been used as an electron stain for en bloc staining as well as for staining ultrathin sections in conjunction with various lead stains (Fig. 1). Present studies reveal that various platinum compounds also show promise as electron stains. Certain platinum compounds have been shown to be effective anti-tumor agents. Of particular interest are the compounds with either uracil or thymine as one of the ligands (cis-Pt(II)-uracil; cis-Pt(II)-thymine). These compounds are amorphous, highly soluble in water and often exhibit an intense blue coloration. These compounds show enough electron density to be used as stains for electron microscopy. Most of the studies are based on various cell lines (human AV, cells, human lymphoma cells, KB cells, Sarcoma-180 ascites cells, chick fibroblasts and HeLa cells) while studies on tissue blocks are in progress.


Author(s):  
Gustav Ofosu

Platinum-thymine has been found to be a potent antitumor agent, which is quite soluble in water, and lack nephrotoxicity as the dose-limiting factor. The drug has been shown to interact with DNA and inhibits DNA, RNA and protein synthesis in mammalian cells in vitro. This investigation was undertaken to elucidate the cytotoxic effects of piatinum-thymine on sarcoma-180 cells in vitro ultrastructurally, Sarcoma-180 tumor bearing mice were treated with intraperitoneal injection of platinum-thymine 40mg/kg. A concentration of 60μg/ml dose of platinum-thymine was used in in vitro experiments. Treatments were at varying time intervals of 3, 7 and 21 days for in vivo experiments, and 30, 60 and 120 min., 6, 12, and 24th in vitro. Controls were not treated with platinum-thymine.Electron microscopic analyses of the treated cells in vivo and in vitro showed drastic cytotoxic effect.


Sign in / Sign up

Export Citation Format

Share Document