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RAGE Inhibitors for Targeted Therapy of Cancer: A Comprehensive Review
Tabrez Faruqui1, Mohd Sajid Khan2, Yusuf Akhter3
1Department of Biosciences, Integral University, Dasauli, P.O. Basha, Kursi Road, Lucknow 226026, Uttar Pradesh, India.
Abstract:
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.
Insights
The receptor for advanced glycation end products (RAGE) is overexpressed in cancers, promoting tumor growth and metastasis. Inhibiting RAGE-ligand interactions offers a promising strategy for cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- The receptor for advanced glycation end products (RAGE) is an immunoglobulin family member implicated in cancer.
- RAGE expression is elevated in various cancers, particularly in the lung, and correlates with inflammation.
- RAGE binds diverse ligands, including advanced glycation end products and S100 proteins, mediating inflammatory and cellular stress responses.
Purpose of the Study:
- To review the multifaceted roles of RAGE and its ligands in cancer pathogenesis.
- To elucidate the significant involvement of RAGE in cancer development and progression.
- To explore the therapeutic potential of targeting RAGE-ligand interactions.
Main Methods:
- Literature review of studies investigating RAGE and its ligands in cancer.
- Analysis of RAGE expression patterns in different cancer types.
- Examination of signaling pathways initiated by RAGE activation.
Main Results:
- RAGE acts as a critical signaling node, promoting carcinogenesis, tumor growth, and metastasis.
- RAGE ligands contribute to cellular stress and growth signaling, driving cancer progression.
- Evidence suggests RAGE is a key player in initiating and sustaining cancer development.
Conclusions:
- Targeting the RAGE-ligand axis presents a viable therapeutic strategy for cancer.
- Inhibiting RAGE interactions can potentially hinder cancer development and progression.
- Further research into RAGE pathways may yield novel cancer treatments.
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