Prognostic Potential and Tumor Growth-Inhibiting Effect of Plasma Advanced Glycation End Products in Non-Small Cell Lung Carcinoma

被引:28
作者
Bartling, Babett [1 ]
Hofmann, Hans-Stefan [1 ,2 ]
Sohst, Antonia [1 ]
Hatzky, Yvonne [1 ]
Somoza, Veronika [3 ]
Silber, Rolf-Edgar [1 ]
Simm, Andreas [1 ]
机构
[1] Univ Halle Wittenberg, Dept Cardio & Thorac Surg, Univ Hosp Halle Saale, Halle, Saale, Germany
[2] Hosp Barmherzige Bruder Regensburg, Dept Thorac Surg, Regensburg, Germany
[3] Univ Vienna, A-1010 Vienna, Austria
关键词
MAILLARD REACTION-PRODUCTS; OXIDATIVE STRESS; METABOLIC TRANSIT; PRONYL-LYSINE; CANCER; PROTEIN; RECEPTOR; HEALTH; CLASSIFICATION; METHYLGLYOXAL;
D O I
10.2119/molmed.2011.00085
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
The plasma fluorescence related to the standard fluorescence of advanced glycation end products (AGES) is a simple measurable blood parameter for distinct diseases but its importance in human cancer, including non-small cell lung carcinoma (NSCLC), is unknown. Plasma samples of 70 NSCLC patients who underwent resection surgery of the tumor were analyzed for the distinct AGE-related fluorescence at 370 nm excitation/440 nm emission. In a retrospective study, we tested the prognostic relevance of this AGE-related plasma fluorescence. The effect of circulating AGEs on the NSCLC growth was studied experimentally in vitro and in vivo. NSCLC patients with high (> median) AGE-related plasma fluorescence were characterized by a later reoccurrence of the tumor after curative surgery and a higher survival rate compared with patients with low plasma fluorescence (25% versus 47% 5-y survival, P = 0.011). Treating NSCLC cell spheroids with patients' plasma showed an inverse correlation between the growth of spheroids in vitro and the individual AGE-related fluorescence of each plasma sample. To confirm the impact of circulating AGEs on the NSCLC progression, we studied the NSCLC growth in mice whose circulating AGE level was elevated by AGE-rich diet. In vivo tumorigenicity assays demonstrated that mice with higher levels of circulating AGEs developed smaller tumors than mice with normal AGE levels. The AGE-related plasma fluorescence has prognostic relevance for NSCLC patients in whom the tumor growth-inhibiting effect of circulating AGEs might play a critical role. (C) 2011 The Feinstein Institute for Medical Research, www.feinsteininstitute.org Online address: http://www.molmed.org doi: 10.2119/molmed.2011.00085
引用
收藏
页码:980 / 989
页数:10
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