RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review.
Tabrez FaruquiMohd Sajid KhanYusuf AkhterSalman KhanZeeshan RafiMohd SaeedIhn HanEun Ha ChoiDharmendra Kumar YadavPublished in: International journal of molecular sciences (2022)
The receptor for advanced glycation end products (RAGE) is a member of the immunoglobulin family that is overexpressed in several cancers. RAGE is highly expressed in the lung, and its expression increases proportionally at the site of inflammation. This receptor can bind a variety of ligands, including advanced glycation end products, high mobility group box 1, S100 proteins, adhesion molecules, complement components, advanced lipoxidation end products, lipopolysaccharides, and other molecules that mediate cellular responses related to acute and chronic inflammation. RAGE serves as an important node for the initiation and stimulation of cell stress and growth signaling mechanisms that promote carcinogenesis, tumor propagation, and metastatic potential. In this review, we discuss different aspects of RAGE and its prominent ligands implicated in cancer pathogenesis and describe current findings that provide insights into the significant role played by RAGE in cancer. Cancer development can be hindered by inhibiting the interaction of RAGE with its ligands, and this could provide an effective strategy for cancer treatment.
Keyphrases
- papillary thyroid
- squamous cell
- oxidative stress
- small cell lung cancer
- signaling pathway
- transcription factor
- binding protein
- childhood cancer
- escherichia coli
- staphylococcus aureus
- single cell
- intensive care unit
- mesenchymal stem cells
- poor prognosis
- pseudomonas aeruginosa
- risk assessment
- drug induced
- hepatitis b virus
- candida albicans
- mechanical ventilation