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.

Oncology Letters
|July 15, 2015
PubMed

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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