scholarly journals Differential effects between amphoterin and advanced glycation end products on colon cancer cells

2003 ◽  
Vol 104 (6) ◽  
pp. 722-727 ◽  
Author(s):  
Hiroki Kuniyasu ◽  
Yoshitomo Chihara ◽  
Hideaki Kondo
Keyword(s):  
Colon Cancer ◽  
Cancer Cells ◽  
Advanced Glycation End Products ◽  
Colon Cancer Cells ◽  
Advanced Glycation ◽  
Differential Effects ◽  
Glycation End Products ◽  
End Products

scholarly journals The Genotoxic and Pro-Apoptotic Activities of Advanced Glycation End-Products (MAGE) Measured with Micronuclei Assay Are Inhibited by Their Low Molecular Mass Counterparts

Genes ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 729
Author(s):  
Monika Czech ◽  
Maria Konopacka ◽  
Jacek Rogoliński ◽  
Zbigniew Maniakowski ◽  
Magdalena Staniszewska ◽  
...  
Keyword(s):  
Molecular Mass ◽  
Cancer Cells ◽  
Advanced Glycation End Products ◽  
Human Lymphocytes ◽  
Advanced Glycation ◽  
Control Value ◽  
Genotoxic Activity ◽  
Glycation End Products ◽  
End Products

An association between the cancer invasive activities of cells and their exposure to advanced glycation end-products (AGEs) was described early in some reports. An incubation of cells with BSA–AGE (bovine serum albumin–AGE), BSA–carboxymethyllysine and BSA–methylglyoxal (BSA–MG) resulted in a significant increase in DNA damage. We examined the genotoxic activity of new products synthesized under nonaqueous conditions. These were high molecular mass MAGEs (HMW–MAGEs) formed from protein and melibiose and low molecular mass MAGEs (LMW–MAGEs) obtained from the melibiose and N-α-acetyllysine and N-α-acetylarginine. We have observed by measuring of micronuclei in human lymphocytes in vitro that the studied HMW–MAGEs expressed the genotoxicity. The number of micronuclei (MN) in lymphocytes reached 40.22 ± 5.34 promille (MN/1000CBL), compared to 28.80 ± 6.50 MN/1000 CBL for the reference BSA–MG, whereas a control value was 20.66 ± 1.39 MN/1000CBL. However, the LMW–MAGE fractions did not induce micronuclei formation in the culture of lymphocytes and partially protected DNA against damage in the cells irradiated with X-ray. Human melanoma and all other studied cells, such as bronchial epithelial cells, lung cancer cells and colorectal cancer cells, are susceptible to the genotoxic effects of HMW–MAGEs. The LMW–MAGEs are not genotoxic, while they inhibit HMW–MAGE genotoxic activity. With regard to apoptosis, it is induced with the HMW–MAGE compounds, in the p53 independent way, whereas the low molecular mass product inhibits the apoptosis induction. Further investigations will potentially indicate beneficial apoptotic effect on cancer cells.

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