Plasma lyso-phosphatidylcholine concentration is decreased in cancer patients with weight loss and activated inflammatory status

被引:139
作者
Taylor, Lenka A. [1 ]
Arends, Jann [1 ]
Hodina, Arwen K. [1 ]
Unger, Clemens [1 ]
Massing, Ulrich [1 ]
机构
[1] Tumor Biol Ctr, Dept Clin Res, D-79106 Freiberg, Germany
关键词
D O I
10.1186/1476-511X-6-17
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: It has been observed that ras-transformed cell lines in culture have a higher phosphatidylcholine (PC) biosynthesis rate as well as higher PC-degradation rate (increased PC-turnover) than normal cells. In correspondence to these findings, the concentrations of the PC-degradation product lyso-phosphatidylcholine (LPC) in cancer patients were found to be decreased. Our objective was the systematic investigation of the relationship between LPC and inflammatory and nutritional parameters in cancer patients. Therefore, plasma LPC concentrations were assessed in 59 cancer patients and related to nutritional and inflammatory parameters. To determine LPC in blood plasma we developed and validated a HPTLC method. Results: Average plasma LPC concentration was 207 +/- 59 mu M which corresponds to the lower limit of the reported range in healthy subjects. No correlation between LPC and age, performance status, body mass index (BMI) or fat mass could be seen. However, LPC correlated inversely with plasma C-reactive protein (CRP) and whole blood hydrogen peroxides (HPO). Further, a negative correlation could be observed between LPC and whole body extra cellular fluid volume (ECF) as well as with relative change in body weight since cancer diagnosis. Conclusion: In conclusion, LPC concentrations were decreased in cancer patients. LPC plasma concentrations correlated with weight loss and inflammatory parameters and, therefore, might be a general indicator of severity of malignant disease.
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页数:8
相关论文
共 27 条
[11]   Endothelial lipase releases saturated and unsaturated fatty acids of high density lipoprotein phosphatidylcholine [J].
Gauster, M ;
Rechberger, G ;
Sovic, A ;
Hörl, G ;
Steyrer, E ;
Sattler, W ;
Frank, S .
JOURNAL OF LIPID RESEARCH, 2005, 46 (07) :1517-1525
[12]   c-Ha-ras oncogene expression increases choline uptake, CTP:phosphocholine cytidylyltransferase activity and phosphatidylcholine biosynthesis in the immortalized human keratinocyte cell line HaCaT [J].
Geilen, CC ;
Wieder, T ;
Boremski, S ;
Wieprecht, M ;
Orfanos, CE .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1996, 1299 (03) :299-305
[13]  
Guyton A C, 1980, Contrib Nephrol, V21, P6
[14]  
KOTTING J, 1992, ALKYLPHOSPHOCHOLINES, P131
[15]  
KRIAT M, 1993, J LIPID RES, V34, P1009
[16]   Application of 31P MRS to the analysis of phospholipid changes in plasma of patients with acute leukemia [J].
Kuliszkiewicz-Janus, M ;
Tuz, MA ;
Baczynski, S .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2005, 1737 (01) :11-15
[17]  
KuliszkiewiczJanus M, 1996, ANTICANCER RES, V16, P1587
[18]   Reference values of fat-free and fat masses by bioelectrical impedance analysis in 3393 healthy subjects [J].
Pichard, C ;
Kyle, UG ;
Bracco, D ;
Slosman, DO ;
Morabia, A ;
Schutz, Y .
NUTRITION, 2000, 16 (04) :245-254
[19]  
Raffelt K, 2000, NMR BIOMED, V13, P8, DOI 10.1002/(SICI)1099-1492(200002)13:1<8::AID-NBM602>3.0.CO
[20]  
2-X