| Literature DB >> 25111846 |
Hanbei Chen1, Lifang Wu2, Yakui Li2, Jian Meng2, Ning Lin1, Dianqiang Yang3, Yemin Zhu2, Xiaoyong Li1, Minle Li2, Ye Xu4, Yuchen Wu4, Xuemei Tong5, Qing Su6.
Abstract
Diabetic patients have increased levels of advanced glycation end products (AGEs) and the role of AGEs in regulating cancer cell proliferation is unclear. Here, we found that treating colorectal and liver cancer cells with AGEs promoted cell proliferation. AGEs stimulated both the expression and activation of a key transcription factor called carbohydrate responsive element binding protein (ChREBP) which had been shown to promote glycolytic and anabolic activity as well as proliferation of colorectal and liver cancer cells. Using siRNAs or the antagonistic antibody for the receptor for advanced glycation end-products (RAGE) blocked AGEs-induced ChREBP expression or cell proliferation in cancer cells. Suppressing ChREBP expression severely impaired AGEs-induced cancer cell proliferation. Taken together, these results demonstrate that AGEs-RAGE signaling enhances cancer cell proliferation in which AGEs-mediated ChREBP induction plays an important role. These findings may provide new explanation for increased cancer progression in diabetic patients.Entities:
Keywords: Advanced glycation end products; Cancer; Carbohydrate responsive element binding protein; Diabetes mellitus; Proliferation; Receptor for advanced glycation end-products
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Year: 2014 PMID: 25111846 DOI: 10.1016/j.mce.2014.07.021
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102