2014
DOI: 10.1016/j.mce.2014.07.021
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Advanced glycation end products increase carbohydrate responsive element binding protein expression and promote cancer cell proliferation

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Cited by 47 publications
(46 citation statements)
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“…High glucose levels also enhance resistance to 5-fluoruracil-induced apoptosis [63]. AGE-induced CRC cell proliferation requires carbohydrate response element-binding protein (ChREBP) [64], a key transcription factor also involved in DKD [65]. The polyol and hexosamine pathways, which increase glucose oxidation, are upregulated in diabetes target organ epithelial cells [54] and in colon cancer [66].…”
Section: Potential Molecular Mechanisms Of the Association Between Dmmentioning
confidence: 99%
“…High glucose levels also enhance resistance to 5-fluoruracil-induced apoptosis [63]. AGE-induced CRC cell proliferation requires carbohydrate response element-binding protein (ChREBP) [64], a key transcription factor also involved in DKD [65]. The polyol and hexosamine pathways, which increase glucose oxidation, are upregulated in diabetes target organ epithelial cells [54] and in colon cancer [66].…”
Section: Potential Molecular Mechanisms Of the Association Between Dmmentioning
confidence: 99%
“…AGEs in general have been implicated in the development of diabetes (17, 18) and in ocular (19), renal (20), cardiovascular (21), and some neurodegenerative disorders (22), as well as in several cancers (23, 24). For their part, glycer-AGEs have been shown to be cytotoxic in vitro (25, 26) and findings from animal studies suggest involvement in the pathogenesis of insulin resistance and diabetes (27) as well as its complications (28).…”
Section: Introductionmentioning
confidence: 99%
“…The differences between the results of PFMA and PGMA are probably related to the higher hydrolysis rate and fructose release rate to the culture medium. Nutrients such as glucose, fructose and fatty acids are reported to stimulate both expression and activation of the key transcription factor, which is reported to increase cell proliferation . Therefore, neither the hydrogels nor their degradation products in culture medium are cytotoxic, making PFMA and PGMA hydrogels suitable materials for biomedical applications.…”
Section: Resultsmentioning
confidence: 99%