Abstract
Originalsprog | Engelsk |
---|---|
Tidsskrift | Cancer Research |
Vol/bind | 55 |
Udgave nummer | 8 |
Sider (fra-til) | 1664-9 |
Antal sider | 5 |
ISSN | 0008-5472 |
Status | Udgivet - 1995 |
Bibliografisk note
Keywords: Animals; Breast Neoplasms; Cell Division; Cell Line; Drug Implants; Energy Metabolism; Estradiol; Female; Humans; Kinetics; Magnetic Resonance Spectroscopy; Mice; Mice, Nude; Ovariectomy; Phosphates; Phosphocreatine; Phosphorus; Ribonucleotides; Transplantation, Heterologous; Tumor Cells, CulturedCitationsformater
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I: Cancer Research, Bind 55, Nr. 8, 1995, s. 1664-9.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
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TY - JOUR
T1 - Effect of estrogen withdrawal on energy-rich phosphates and prediction of estrogen dependence monitored by in vivo 31P magnetic resonance spectroscopy of four human breast cancer xenografts
AU - Kristensen, C A
AU - Kristjansen, P E
AU - Brünner, N
AU - Clarke, R
AU - Spang-Thomsen, M
AU - Quistorff, B
N1 - Keywords: Animals; Breast Neoplasms; Cell Division; Cell Line; Drug Implants; Energy Metabolism; Estradiol; Female; Humans; Kinetics; Magnetic Resonance Spectroscopy; Mice; Mice, Nude; Ovariectomy; Phosphates; Phosphocreatine; Phosphorus; Ribonucleotides; Transplantation, Heterologous; Tumor Cells, Cultured
PY - 1995
Y1 - 1995
N2 - The effect of estrogen withdrawal on energy metabolism was studied in four human breast cancer xenografts: the estrogen-dependent MCF-7 and ZR75-1 and the estrogen-independent ZR75/LCC-3 and MDA-MB-231. The tumors were grown in ovariectomized nude mice with a s.c. implanted estrogen pellet. After Gompertzian growth was verified, the estrogen pellet was removed from half of the animals. In vivo 31P magnetic resonance spectroscopy of the tumors was performed 1 day before and on days 2, 6, and 14 after estrogen removal. Estrogen withdrawal induced a significant increase in the nucleoside triphosphate:Pi ratio in the two estrogen-dependent xenografts, whereas this ratio remained unchanged in the estrogen-independent tumors. In ZR75/LCC-3 tumors a slight decrease in nucleoside triphosphate:Pi was observed following onset of estrogen stimulation after initial growth without estrogen. Extracts of freeze-clamped tumors prepared 14 days after estrogen removal were analyzed for ATP and phosphocreatine content. Our findings suggest a correlation between estrogen withdrawal and the steady-state concentrations of ATP, phosphocreatine, and Pi in human breast cancer xenografts. Discrimination analysis of the pretherapeutic spectra enabled us to identify the tumor line and the estrogen dependence of the tumors in 80-90% of all cases.
AB - The effect of estrogen withdrawal on energy metabolism was studied in four human breast cancer xenografts: the estrogen-dependent MCF-7 and ZR75-1 and the estrogen-independent ZR75/LCC-3 and MDA-MB-231. The tumors were grown in ovariectomized nude mice with a s.c. implanted estrogen pellet. After Gompertzian growth was verified, the estrogen pellet was removed from half of the animals. In vivo 31P magnetic resonance spectroscopy of the tumors was performed 1 day before and on days 2, 6, and 14 after estrogen removal. Estrogen withdrawal induced a significant increase in the nucleoside triphosphate:Pi ratio in the two estrogen-dependent xenografts, whereas this ratio remained unchanged in the estrogen-independent tumors. In ZR75/LCC-3 tumors a slight decrease in nucleoside triphosphate:Pi was observed following onset of estrogen stimulation after initial growth without estrogen. Extracts of freeze-clamped tumors prepared 14 days after estrogen removal were analyzed for ATP and phosphocreatine content. Our findings suggest a correlation between estrogen withdrawal and the steady-state concentrations of ATP, phosphocreatine, and Pi in human breast cancer xenografts. Discrimination analysis of the pretherapeutic spectra enabled us to identify the tumor line and the estrogen dependence of the tumors in 80-90% of all cases.
M3 - Journal article
C2 - 7712472
SN - 0008-5472
VL - 55
SP - 1664
EP - 1669
JO - Cancer Research
JF - Cancer Research
IS - 8
ER -