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GADD45α-mediated promoter demethylation. These results revealed that commercial AGEs can partially represent the role of endogenous AGEs in this study. Furthermore, the term AGEs applies to a broad range of advanced glycation end products. The effect of
Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
Department of Medicine and Therapeutics, Hong Kong Institute of Diabetes and Obesity , Li Ka Shing Institute of Health Sciences, Department of Epidemiology and Biostatistics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China
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of advanced glycation end products (AGEs), which have been implicated in development of liver disease ( Hyogo & Yamagishi 2008 ). Further experimental studies are needed to study the effects of AGEs on promoting HBV-associated HCC risk in diabetes
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endothelial dysfunction. These factors cooperate and contribute to CRC development through decreased immune surveillance, cell transformation, metastasis and angiogenesis. AGEs, advanced glycation end products; CRC, colorectal cancer; T2D, type 2 diabetes; ROS
Instituto de Endocrinología IEMYR, Quito, Ecuador
Maastricht University, Maastricht, The Netherlands
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-lasting excess glucose and insulin serum levels result in the generation of advanced glycation end products that distort bodily proteins, hence originating permanent and usually irreversible tissue damage ( Gallagher & LeRoith 2015 ). Because of their higher
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Deeley Research Centre, Translational Gastroenterology Unit, Department of Biochemistry and Medical Genetics and the Manitoba Institute of Cell Biology, Department of Biochemistry and Microbiology, Department of Pathology and Laboratory Medicine, British Columbia Cancer Agency, 2410 Lee Avenue, Victoria, British Columbia, Canada V8R 6V5
Deeley Research Centre, Translational Gastroenterology Unit, Department of Biochemistry and Medical Genetics and the Manitoba Institute of Cell Biology, Department of Biochemistry and Microbiology, Department of Pathology and Laboratory Medicine, British Columbia Cancer Agency, 2410 Lee Avenue, Victoria, British Columbia, Canada V8R 6V5
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by the receptor for advanced glycation end products and potentiates inflammation with highly homologous but functionally distinct S100A15 . Journal of Immunology 181 1499 – 1506 . ( doi:10.4049/jimmunol.181.2.1499 ). Wolk K Witte E Wallace
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proteins on androgen-mediated gene activation in prostate cancer cells . Oncogene 20 3880 – 3887 . Guh JY Huang JS Chen HC Hung WC Lai YH Chuang LY 2001 Advanced glycation end product-induced proliferation in NRK-49F cells is dependent on the
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signals through TLR4, TLR9 and the receptor for advanced glycation end-products (RAGE) to promote further maturation of DCs ( Kang et al. 2013 ). However, the molecular translocation and signaling mechanisms that surround HMGB1 in ICD are complex and