An interaction of cis platin and radiation in two rat yolk sac tumour cell lines with different radiosensitivities in vitro

1996 ◽  
Vol 70 (6) ◽  
pp. 747-753 ◽  
Author(s):  
S. NAKAMOTO
Keyword(s):  
Cell Lines ◽  
Tumour Cell ◽  
Yolk Sac ◽  
Tumour Cell Lines ◽  
Yolk Sac Tumour

Immunophenotype of Mammary Tumour Cell Lines for In-Vitro Analysis Using Three Different Techniques

2020 ◽  
Vol 174 ◽  
pp. 184
Author(s):  
F. Torrigiani ◽  
A. Sammarco ◽  
M.E. Gelain ◽  
F. Bonsembiante ◽  
R. Zanetti ◽  
...  
Keyword(s):  
Cell Lines ◽  
Tumour Cell ◽  
Mammary Tumour ◽  
Tumour Cell Lines ◽  
Vitro Analysis ◽  
In Vitro Analysis

scholarly journals Novel O-methyl goniofufurone and 7-epi-goniofufurone derivatives: synthesis, in vitro cytotoxicity and SAR analysis

MedChemComm ◽  
2018 ◽  
Vol 9 (12) ◽  
pp. 2017-2027
Author(s):  
Jovana Francuz ◽  
Mirjana Popsavin ◽  
Sanja Djokić ◽  
Vesna Kojić ◽  
Tatjana Srdić-Rajić ◽  
...  
Keyword(s):  
Cell Lines ◽  
Tumour Cell ◽  
Methoxy Group ◽  
Antitumour Activity ◽  
In Vitro Cytotoxicity ◽  
Human Tumour ◽  
Tumour Cell Lines ◽  
Sar Analysis ◽  
Human Tumour Cell Lines

Novel goniofufurone (1) and 7-epi-goniofufurone (2) derivatives bearing a methoxy group at the C-5 and/or C-7 positions were prepared and their in vitro antitumour activity against some human tumour cell lines was evaluated.

scholarly journals Synthesis, Characterization and High In Vitro Antitumour Activity of Novel Triphenyltin Carboxylates

1994 ◽  
Vol 1 (4) ◽  
pp. 305-309 ◽  
Author(s):  
Marcel Gielen ◽  
Abdelaziz El Khloufi ◽  
Monique Biesemans ◽  
Abdeslam Bouhdid ◽  
Dick de Vos ◽  
...  
Keyword(s):  
Colon Carcinoma ◽  
Cell Lines ◽  
Tumour Cell ◽  
Antitumour Activity ◽  
Human Tumour ◽  
Tumour Cell Lines ◽  
Human Tumour Cell Lines ◽  
Mcf 7

The synthesis and spectral characterization of six novel triphenyltin compounds are described. The in vitro antitumour activity of three of these compounds against two human tumour cell lines, MCF-7, a mammary tumour, and WiDr, a colon carcinoma, was determined. All three compounds are more active than cis-platin, etoposide and doxorubicin against both tumour cell lines. They are as active as mitomycin C against WiDr, but less active against MCF-7.

In-vitro anti-proliferative effects of some anti-tumour drugs on feline mammary tumour cell lines

1999 ◽  
Vol 66 (3) ◽  
pp. 169-174 ◽  
Author(s):  
J.S MULEYA ◽  
M NAKAICHI ◽  
Y TAURA ◽  
R YAMAGUCHI ◽  
S NAKAMA
Keyword(s):  
Cell Lines ◽  
Tumour Cell ◽  
Mammary Tumour ◽  
Tumour Cell Lines

scholarly journals Di-n-Butyl-, Tri-n-Butyl- and Triphenyltin dl-Terebates: Synthesis, Characterization and In Vitro Antitumour Activity

1997 ◽  
Vol 4 (4) ◽  
pp. 193-197 ◽  
Author(s):  
Marcel Gielen ◽  
Huairang Ma ◽  
Abdeslam Bouhdid ◽  
Hassan Dalil ◽  
Monique Biesemans ◽  
...  
Keyword(s):  
Cell Lines ◽  
Tumour Cell ◽  
Antitumour Activity ◽  
Human Tumour ◽  
Tumour Cell Lines ◽  
Human Tumour Cell Lines

Di-n-butyltin, tri-n-butyltin and triphenyltin terebates were screened against several human tumour cell lines and found comparably or more active than carboplatin, cis-platin, 5-fluorouracil, methotrexate and doxorubicin, some reference compounds used clinically.

l-Asparaginyl-Trna Synthetase and l-Asparagine Synthetase Activities of l-Asparaginase-Sensitive and -Resistant Forms of the Mouse Gardner Lymphoma 6C3HED

1979 ◽  
Vol 56 (6) ◽  
pp. 539-545 ◽  
Author(s):  
M. R. Davies ◽  
Lucy P. Lambert ◽  
R. D. Marshall
Keyword(s):  
Cell Lines ◽  
Tumour Cell ◽  
Trna Synthetase ◽  
Asparagine Synthetase ◽  
Ascites Fluid ◽  
Synthetase Activity ◽  
Early Passage ◽  
Tumour Cell Lines ◽  
Cells Cultured

1. The mouse Gardner lymphoma 6C3HED was grown in ascites fluid in a form sensitive to the action of l-asparaginase (line 1), in another form which was resistant to l-asparaginase (line 2) and in a third form with partial sensitivity to l-asparaginase (line 3). 2. The l-asparaginyl-tRNA synthetase activities of extracts of the tumour cells, cultured both in the mouse and in vitro, were determined. Two of the lines, 1 and 3, in early passage numbers, showed a derepression mechanism involving l-asparagine. Mutation occurred with these lines resulting in the l-asparaginyl-tRNA synthetase activity of all the tumour cell lines being the same. 3. Cells of line 1 had low l-asparagine synthetase activity, which was unchanged by altering the supply of l-asparagine in vitro. Cells of lines 2 and 3 exhibited l-asparagine synthetase activities, which changed with the supply of l-asparagine. 4. It is not certain that l-asparagine synthetase activity of l-asparaginase-sensitive cells is controlled by l-asparaginyl-tRNA acting as a corepressor.

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