Steroid responsiveness of the human cell line NHIK 3025

1981 ◽  
Vol 97 (4) ◽  
pp. 551-558
Author(s):  
Kjetill Østgaard ◽  
Einar Wibe ◽  
Kristen B. Eik-Nes

Abstract. The human cell line NHIK 3025, derived from a carcinoma of the uterine cervix, contains a glucocorticoid and an androgen receptor. The effect of various natural and synthetic steroid hormones and antihormones on growth rate of these cells was therefore investigated. Cells grown in Eagle's MEM with 10% foetal calf serum exhibited reduced growth when cultured with dexamethasone due to prolongation of the cell cycle. Glucocorticoid anti-inducers like progesterone had no significant effect on cell growth. Methyltrienolone (R 1881) or 5α-dihydrotestosterone did not affect cell proliferation. The reported shortening of the cell cycle by testosterone is probably not directly connected with activation of the androgen receptor present, but possibly dependent on metabolic conversion of testosterone to the more potent growth stimulator 4-androstene-3β, 17β-diol. The effect of several anti-androgens was also studied. The non-steroidal anti-androgens flutamide and SCH 16483 had no significant effect on cell proliferation. It was, however, found that a number of steroid antiandrogens, including R2956, stimulated cell growth. A significant stimulatory effect by R2956 was seen within the first cell generation, 4-androstene-3β,17β-diol had to be present during 2 days, and testosterone for even longer times before a similar effect on cell growth could be obtained.

1981 ◽  
Vol 48 (1) ◽  
pp. 281-290
Author(s):  
K. Ostgaard ◽  
E. Wibe ◽  
T. Lindmo ◽  
K.B. Eik-Nes

The median cell cycle of synchronized NHIK3025 cells grown in Eagle's MEM with 10% foetal calf serum was 23.6 h, compared to 18 h observed earlier in Puck's E2a medium with 30% serum (20% human and 10% horse). This difference is due to prolongation of both G1 and G2 in the MEM type medium. Testosterone and 4-androstene-3 beta, 17 beta-diol reduced the cell cycle of synchronized populations of NHIK3025 cultured in MEM type medium. Dexamethasone gave cell cycle prolongation while estradiol had no effect. These results are in accordance with steroid-induced changes in growth of asynchronous cell populations observed earlier. The androgen growth stimulation was partly due to a shortening of G2 but was not exclusively located in one particular phase of the cell cycle.


Toxicology ◽  
1982 ◽  
Vol 24 (3-4) ◽  
pp. 281-292 ◽  
Author(s):  
Karin Jakobsen ◽  
Oddmund Bakke ◽  
Kjetill Østgaard ◽  
Linda R. White ◽  
Kristen B. Eik-nes

1978 ◽  
Vol 11 (3) ◽  
pp. 309-323 ◽  
Author(s):  
E. Mulder ◽  
M.J. Peters ◽  
J. De Vries ◽  
H.J. Van Der Molen ◽  
K. Østgaard ◽  
...  

2017 ◽  
Vol 18 (8) ◽  
pp. 560-570 ◽  
Author(s):  
Gabrielle Dias Salton ◽  
Claudia Cilene Fernandes Correia Laurino ◽  
Nicolás Oliveira Mega ◽  
Andrés Delgado-Cañedo ◽  
Niclas Setterblad ◽  
...  

Cytometry ◽  
2005 ◽  
Vol 2 (6) ◽  
pp. 426-430 ◽  
Author(s):  
R. Zippel ◽  
E. Martegani ◽  
M. Vanoni ◽  
G. Mazzini ◽  
L. Alberghina

1981 ◽  
Vol 89 (2) ◽  
pp. 256-260 ◽  
Author(s):  
T W James ◽  
R Bohman

Using rhodamine 123 to stain mitochondria of the human cell line HL-60, we have followed their increase over the cell cycle by flow cytometry. A near-linear synthesis of mitochondrial mass was shown to occur over the cell cycle. A comparison with the cell's DNA synthesis pattern obtained by the same technique established a common time-base. The mitochondrial synthesis curve changes with culture age. As a control, thd dye was tested for its binding specificity and for its use to resolve mitochondria microscopically. Its stoichiometric range was established and, above 0.25 microgram/ml, it was shown to reduce growth rate and cell viability in culture.


2001 ◽  
Vol 298 (1) ◽  
pp. 93-102 ◽  
Author(s):  
B.M.G. Blankvoort ◽  
E.M. de Groene ◽  
A.P. van Meeteren-Kreikamp ◽  
R.F. Witkamp ◽  
R.J.T. Rodenburg ◽  
...  

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