RAGE and its ligands in cancer – Culprits, biomarkers, or therapeutic targets?

26Citations
Citations of this article
19Readers
Mendeley users who have this article in their library.

Abstract

Receptor for advanced glycation end products (RAGE) plays a central role in the regulation of tissue homeostasis, regeneration and resolution of inflammation, but under pathological conditions RAGE-mediated pathways may induce diminished apoptosis, but enhanced autophagy and cell necrosis. These mechanisms may contribute to malignant transformation, cancer progression and metastases. Soluble RAGE may bind natural RAGE ligands and counteract some of the RAGE-mediated effects. Activation of RAGE was demonstrated in different types of cancer (including colon, pancreatic and breast cancer). Expression of RAGE and serum levels of soluble RAGE may serve as cancer biomarkers and strategies aimed at interfering with RAGE signaling might be promising anticancer drugs.

Author supplied keywords

Cite

CITATION STYLE

APA

Tesarova, P., Cabinakova, M., Mikulova, V., Zima, T., & Kalousova, M. (2015). RAGE and its ligands in cancer – Culprits, biomarkers, or therapeutic targets? Neoplasma. Cancer Research Institute Slovak Acad. of Sciences. https://doi.org/10.4149/neo_2015_061

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free