TY - JOUR
T1 - Information from combined 1H and 31P NMR studies of cell extracts
T2 - Differences in metabolism between drug-sensitive and drug-resistant MCF-7 human breast cancer cells
AU - Kaplan, Ofer
AU - van Zijl, Peter C.M.
AU - Cohen, Jack S.
PY - 1990/6/15
Y1 - 1990/6/15
N2 - Combined analysis of both 1H and 31P NMR spectra of extracts of drug-sensitive and multidrug-resistant MCF-7 human breast cancer cells enabled quantitative comparisons between the concentrations of major metabolites, as well as of their precursors. In resistant cells high energy phosphorus compounds, phosphocreatine and ATP, and also their precursors, creatine and ADP, were elevated compared to the sensitive cells. In phospholipid metabolism, the sensitive cells showed higher phosphocholine and phosphoethanolamine concentrations than the resistant cells, but choline levels were similar. These results delineated the differences in control of metabolic pathways between drug-sensitive and drug-resistant cells.
AB - Combined analysis of both 1H and 31P NMR spectra of extracts of drug-sensitive and multidrug-resistant MCF-7 human breast cancer cells enabled quantitative comparisons between the concentrations of major metabolites, as well as of their precursors. In resistant cells high energy phosphorus compounds, phosphocreatine and ATP, and also their precursors, creatine and ADP, were elevated compared to the sensitive cells. In phospholipid metabolism, the sensitive cells showed higher phosphocholine and phosphoethanolamine concentrations than the resistant cells, but choline levels were similar. These results delineated the differences in control of metabolic pathways between drug-sensitive and drug-resistant cells.
UR - http://www.scopus.com/inward/record.url?scp=0025196187&partnerID=8YFLogxK
U2 - 10.1016/0006-291X(90)90343-L
DO - 10.1016/0006-291X(90)90343-L
M3 - Article
C2 - 2357212
AN - SCOPUS:0025196187
SN - 0006-291X
VL - 169
SP - 383
EP - 390
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -