by Ruiz-Cabello, J, Berghmans, K, Kaplan, O, Lippman, M E, Clarke, R and Cohen, J S
Abstract:
Many breast tumors appear to progress from estrogen-dependent growth to a more malignant phenotype characterized by estrogen-independent growth, antiestrogen resistance, and a high metastatic potential. Utilizing 31P NMR spectroscopy on human breast cancer cells growing in vitro, we have investigated the effects of 17 beta-estradiol and tamoxifen on the metabolic/bioenergetic spectra of a series of human breast cancer cells that vary in their estrogen and antiestrogen responsiveness. A comparison of baseline spectra associates higher levels of phosphodiesters and UDP-glucosides (e.g. UDP-glucose, UDP-N-acetylglucosamine), and lower phosphocholine/glycerylphosphocholine and phosphocholine/phosphoethanolamine ratios, with the acquisition of estrogen-independent growth in estrogen receptor expressing cells. No metabolic changes are clearly associated with the metastatic phenotype. Whilst estrogen treatment produces no consistently significant spectral changes in any of the cell lines, the estrogen-independent and estrogen-responsive MCF7/MIII cell line responds to tamoxifen treatment by significantly increasing all spectral resonances 30%-40% above baseline values. This may reflect a tamoxifen-induced change to a more differentiated or apoptotic phenotype, or an attempt by the cells to reverse the inhibitory effects of the drug. The ability to detect metabolic changes in response to tamoxifen by NMR spectroscopy may provide a novel means to identify those tumors that are responsive to antiestrogen therapy.
Reference:
Hormone dependence of breast cancer cells and the effects of tamoxifen and estrogen: 31P NMR studies. (Ruiz-Cabello, J, Berghmans, K, Kaplan, O, Lippman, M E, Clarke, R and Cohen, J S), In Breast cancer research and treatment, volume 33, 1995.
Bibtex Entry:
@article{RuizCabello:1995vvb,
author = {Ruiz-Cabello, J and Berghmans, K and Kaplan, O and Lippman, M E and Clarke, R and Cohen, J S},
title = {{Hormone dependence of breast cancer cells and the effects of tamoxifen and estrogen: 31P NMR studies.}},
journal = {Breast cancer research and treatment},
year = {1995},
volume = {33},
number = {3},
pages = {209--217},
month = mar,
affiliation = {Lombardi Cancer Research Center Shady Grove Laboratories, Rockville, MD 20850, USA.},
pmid = {7749148},
language = {English},
rating = {0},
date-added = {2015-03-30T15:04:51GMT},
date-modified = {2017-12-25T10:23:31GMT},
abstract = {Many breast tumors appear to progress from estrogen-dependent growth to a more malignant phenotype characterized by estrogen-independent growth, antiestrogen resistance, and a high metastatic potential. Utilizing 31P NMR spectroscopy on human breast cancer cells growing in vitro, we have investigated the effects of 17 beta-estradiol and tamoxifen on the metabolic/bioenergetic spectra of a series of human breast cancer cells that vary in their estrogen and antiestrogen responsiveness. A comparison of baseline spectra associates higher levels of phosphodiesters and UDP-glucosides (e.g. UDP-glucose, UDP-N-acetylglucosamine), and lower phosphocholine/glycerylphosphocholine and phosphocholine/phosphoethanolamine ratios, with the acquisition of estrogen-independent growth in estrogen receptor expressing cells. No metabolic changes are clearly associated with the metastatic phenotype. Whilst estrogen treatment produces no consistently significant spectral changes in any of the cell lines, the estrogen-independent and estrogen-responsive MCF7/MIII cell line responds to tamoxifen treatment by significantly increasing all spectral resonances 30%-40% above baseline values. This may reflect a tamoxifen-induced change to a more differentiated or apoptotic phenotype, or an attempt by the cells to reverse the inhibitory effects of the drug. The ability to detect metabolic changes in response to tamoxifen by NMR spectroscopy may provide a novel means to identify those tumors that are responsive to antiestrogen therapy.},
url = {http://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=7749148&retmode=ref&cmd=prlinks},
uri = {url{papers3://publication/uuid/0A132A0F-806C-42B4-B397-F0A132782C86}}
}