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RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review
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, inclu...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820344/ https://www.ncbi.nlm.nih.gov/pubmed/36613714 http://dx.doi.org/10.3390/ijms24010266 |
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author | Faruqui, Tabrez Khan, Mohd Sajid Akhter, Yusuf Khan, Salman Rafi, Zeeshan Saeed, Mohd Han, Ihn Choi, Eun-Ha Yadav, Dharmendra Kumar |
author_facet | Faruqui, Tabrez Khan, Mohd Sajid Akhter, Yusuf Khan, Salman Rafi, Zeeshan Saeed, Mohd Han, Ihn Choi, Eun-Ha Yadav, Dharmendra Kumar |
author_sort | Faruqui, Tabrez |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9820344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98203442023-01-07 RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review Faruqui, Tabrez Khan, Mohd Sajid Akhter, Yusuf Khan, Salman Rafi, Zeeshan Saeed, Mohd Han, Ihn Choi, Eun-Ha Yadav, Dharmendra Kumar Int J Mol Sci Review 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. MDPI 2022-12-23 /pmc/articles/PMC9820344/ /pubmed/36613714 http://dx.doi.org/10.3390/ijms24010266 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Faruqui, Tabrez Khan, Mohd Sajid Akhter, Yusuf Khan, Salman Rafi, Zeeshan Saeed, Mohd Han, Ihn Choi, Eun-Ha Yadav, Dharmendra Kumar RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review |
title | RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review |
title_full | RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review |
title_fullStr | RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review |
title_full_unstemmed | RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review |
title_short | RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review |
title_sort | rage inhibitors for targeted therapy of cancer: a comprehensive review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9820344/ https://www.ncbi.nlm.nih.gov/pubmed/36613714 http://dx.doi.org/10.3390/ijms24010266 |
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