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Author Spotlight: Exploring the Role of Inflammation in the Co-occurrence of Primary Sjogren's Syndrome and Lung Adenocarcinoma
Published on: September 20, 2024
Expression of the receptor for advanced glycation end-products and frequency of polymorphism in lung cancer
Hongmei Wang1, Yongchun Li2, Wencheng Yu3
1Department of Respiratory Medicine, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China ; Department of Respiratory Medicine, Qilu Hospital, Shandong University, Jinan, Shandong 250012, P.R. China.
Abstract:
Receptor for advanced glycation end products (RAGE) is associated with the pathogenesis of cancer progression. The pathological effects mediated through RAGE are physiologically inhibited by soluble RAGE (sRAGE). The aim of the present study was to identify the expression of the sRAGE, RAGE and RAGE ligands in serum samples and lung cancer tissue obtained from lung cancer patients. Using ELISA and immunohistochemistry, it was observed that the sRAGE levels were downregulated in the serum, the expression of RAGE was decreased in the lung cancer tissue and the RAGE ligands HMGB1 and S100 were upregulated in cancer tissue. Furthermore, the presence of several selected types of RAGE polymorphism that occur in lung cancers were measured in the tissue samples. An association between the -429T/C and 2184A/G polymorphisms of RAGE and the genesis and progression of lung cancer was identified. The comparison between various histological subtypes and stages of lung cancer was performed with the aim to clarify the biological role of the RAGE gene, and identify a biomarker to aid diagnosis and predict the prognosis for lung cancer patients.
Insights
Levels of soluble Receptor for Advanced Glycation End Products (sRAGE) are lower in lung cancer patients. RAGE gene polymorphisms are linked to lung cancer development and progression, suggesting potential diagnostic biomarkers.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Receptor for Advanced Glycation End Products (RAGE) signaling is implicated in cancer progression.
- Soluble RAGE (sRAGE) acts as a physiological inhibitor of RAGE-mediated pathological effects.
Purpose of the Study:
- To investigate the expression of sRAGE, RAGE, and RAGE ligands in lung cancer patients.
- To analyze RAGE gene polymorphisms in relation to lung cancer genesis and progression.
- To explore RAGE's role in lung cancer diagnosis and prognosis.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) for serum analysis.
- Immunohistochemistry for tissue expression analysis.
- Genotyping for RAGE polymorphisms (-429T/C and 2184A/G).
Main Results:
- sRAGE levels were downregulated in serum samples.
- RAGE expression was decreased in lung cancer tissues.
- RAGE ligands HMGB1 and S100 were upregulated in cancer tissues.
- Specific RAGE polymorphisms (-429T/C and 2184A/G) were associated with lung cancer development and progression.
Conclusions:
- Aberrant expression of sRAGE, RAGE, and its ligands is observed in lung cancer.
- RAGE gene polymorphisms may contribute to lung cancer pathogenesis.
- RAGE pathway components and polymorphisms show potential as diagnostic and prognostic biomarkers for lung cancer.
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