DOI QR코드

DOI QR Code

Serum IL-33 as a Diagnostic and Prognostic Marker in Non-small Cell Lung Cancer

  • Hu, Liang-An (Department of Respiratory Diseases, First Affiliated Hospital of Chongqing Medical University) ;
  • Fu, Yu (Department of Respiratory Diseases, First Affiliated Hospital of Chongqing Medical University) ;
  • Zhang, Dan-Ni (Department of Respiratory Diseases, First Affiliated Hospital of Chongqing Medical University) ;
  • Zhang, Jie (Department of Respiratory Diseases, First Affiliated Hospital of Chongqing Medical University)
  • Published : 2013.04.30

Abstract

Background: Interleukin-33 (IL-33) has recently been implicated in tumor immunity. The aim of this study was to explore the clinical role of serum IL-33 in patients with non-small-cell lung cancer (NSCLC). Methods: Sera collected from 250 healthy volunteers (HV), 256 patients with benign lung diseases (BLD) and 262 NSCLC cases were subjected to IL-33 ELISA and relationships between serum IL-33 and clinical characteristics were evaluated. Results: Circulating IL-33 levels were higher in the NSCLC group in comparison with the HV and BLD groups (p<0.001). Using a cut-off level 68 pg/ml (95% specificity in the HV group), IL-33 showed a good diagnostic performance for NSCLC. Multivariate survival analysis indicated that serum IL-33 was an independent prognostic factor in the entire NSCLC group [hazards ratio (HR) = 0.64 for low versus high IL-33 levels, 95% confidence interval (CI) 0.50-0.82; p<0.001] and in 165 selected patients with locally advanced or metastatic disease receiving chemoradiotherapy or chemotherapy (HR 0.70, 95% CI 0.52-0.94; p=0.013). Conclusions: IL-33 is a promising potential diagnostic and prognostic marker in NSCLC, independent of the therapeutic intervention.

Keywords

References

  1. Bharti A, Ma PC, Salgia R (2007). Biomarker discovery in lung cancer-promises and challenges of clinical proteomics. Mass Spectrom Rev, 26, 451-66. https://doi.org/10.1002/mas.20125
  2. Carriere V, Roussel L, Ortega N, et al (2007). IL-33, the IL-1-like cytokine ligand for ST2 receptor, is a chromatin-associated nuclear factor in vivo. Proc Natl Acad Sci U S A, 104,282-7. https://doi.org/10.1073/pnas.0606854104
  3. Choi YS, Choi HJ, Min JK, et al (2009). Interleukin-33 induces angiogenesis and vascular permeability through ST2/ TRAF6-mediated endothelial nitric oxide production. Blood, 114, 3117-26. https://doi.org/10.1182/blood-2009-02-203372
  4. Dinarello CA (1998). Interleukin-1, interleukin-1 receptors and interleukin-1 receptor antagonist. Int Rev Immunol, 16, 457-99. https://doi.org/10.3109/08830189809043005
  5. Filipits M, Pirker R (2011). Predictive markers in the adjuvant therapy of non-small cell lung cancer. Lung Cancer, 74, 355-63. https://doi.org/10.1016/j.lungcan.2011.06.005
  6. Grunnet M, Sorensen JB (2012). Carcinoembryonic antigen (CEA) as tumor marker in lung cancer. Lung Cancer, 76, 138-43. https://doi.org/10.1016/j.lungcan.2011.11.012
  7. Hoffman PC, Mauer AM ,Vokes EE (2000). Lung cancer. Lancet, 355, 479-85. https://doi.org/10.1016/S0140-6736(00)82038-3
  8. Indovina P, Marcelli E, Maranta P, Tarro G (2011). Lung cancer proteomics: recent advances in biomarker discovery. Int J Proteomics, 2011, 726869.
  9. Jemal A, Siegel R, Xu J, Ward E (2010).Cancer statistics, 2010. CA Cancer J Clin, 60, 277-300. https://doi.org/10.3322/caac.20073
  10. Jovanovic I, Radosavljevic G, Mitrovic M, et al (2011). ST2 deletion enhances innate and acquired immunity to murine mammary carcinoma. Eur J Immunol, 41, 1902-12. https://doi.org/10.1002/eji.201141417
  11. Kuchler AM, Pollheimer J, Balogh J, et al (2008). Nuclear interleukin-33 is generally expressed in resting endothelium but rapidly lost upon angiogenic or proinflammatory activation. Am J Pathol, 173, 1229-42. https://doi.org/10.2353/ajpath.2008.080014
  12. Lee S, Kang J, Cho M, et al (2009). Profiling of transcripts and proteins modulated by K-ras oncogene in the lung tissues of K-ras transgenic mice by omics approaches. Int J Oncol, 34, 161-72.
  13. Lopez-Gonzalez A, Ibeas Millan P, Cantos B, Provencio M (2012). Surveillance of resected non-small cell lung cancer. Clin Transl Oncol, 14, 721-5. https://doi.org/10.1007/s12094-012-0841-z
  14. Oguz A, Unal D, Tasdemir A, et al (2013). Lack of any Association between Blood Groups and Lung Cancer, Independent of Histology. Asian Pac J Cancer Prev, 14, 453-6. https://doi.org/10.7314/APJCP.2013.14.1.453
  15. Schmitz J, Owyang A, Oldham E, et al (2005). IL-33, an interleukin-1-like cytokine that signals via the IL-1 receptorrelated protein ST2 and induces T helper type 2-associated cytokines. Immunity, 23, 479-90. https://doi.org/10.1016/j.immuni.2005.09.015
  16. Srivastava S, Salim N, Robertson MJ (2010). Interleukin-18: biology and role in the immunotherapy of cancer. Curr Med Chem, 17, 3353-7. https://doi.org/10.2174/092986710793176348
  17. Sun P, Ben Q, Tu S, et al (2011). Serum interleukin-33 levels in patients with gastric cancer. Dig Dis Sci, 56, 3596-601. https://doi.org/10.1007/s10620-011-1760-5
  18. Tufman A, Huber RM (2010). Biological markers in lung cancer: A clinician's perspective. Cancer Biomark, 6, 123-35.

Cited by

  1. Clinical Observations on the Association Between Diagnosis of Lung Cancer and Serum Tumor Markers in Combination vol.14, pp.7, 2013, https://doi.org/10.7314/APJCP.2013.14.7.4369
  2. Correlations Between Serum IL33 and Tumor Development: a Meta-analysis vol.15, pp.8, 2014, https://doi.org/10.7314/APJCP.2014.15.8.3503
  3. The route to pathologies in chronic inflammatory diseases characterized by T helper type 2 immune cells vol.178, pp.2, 2014, https://doi.org/10.1111/cei.12409
  4. Significance of Interleukin-33 and Its Related Cytokines in Patients with Breast Cancers vol.5, pp.1664-3224, 2014, https://doi.org/10.3389/fimmu.2014.00141
  5. Clinical Evaluation of Tumor Markers for Diagnosis in Patients with Non-small Cell Lung Cancer in China vol.16, pp.12, 2015, https://doi.org/10.7314/APJCP.2015.16.12.4891
  6. IL-33 Promotes Gastric Cancer Cell Invasion and Migration Via ST2–ERK1/2 Pathway vol.60, pp.5, 2015, https://doi.org/10.1007/s10620-014-3463-1
  7. Dynamics of the IL-33/ST2 network in the progression of human colorectal adenoma to sporadic colorectal cancer vol.64, pp.2, 2015, https://doi.org/10.1007/s00262-014-1624-x
  8. IL-33 is associated with unfavorable postoperative survival of patients with clear-cell renal cell carcinoma vol.37, pp.8, 2016, https://doi.org/10.1007/s13277-016-4879-3
  9. Interleukin-33 enhances programmed oncosis of ST2L-positive low-metastatic cells in the tumour microenvironment of lung cancer vol.7, pp.1, 2016, https://doi.org/10.1038/cddis.2015.418
  10. Soluble IL-33 receptor sST2 inhibits colorectal cancer malignant growth by modifying the tumour microenvironment vol.7, pp.2041-1723, 2016, https://doi.org/10.1038/ncomms13589
  11. Interleukin-33 in tumorigenesis, tumor immune evasion, and cancer immunotherapy vol.94, pp.5, 2016, https://doi.org/10.1007/s00109-016-1397-0
  12. Overexpression of interleukin-33 is associated with poor prognosis of patients with glioma vol.127, pp.3, 2017, https://doi.org/10.1080/00207454.2016.1175441
  13. Immunotherapeutic Concepts to Target Acute Myeloid Leukemia: Focusing on the Role of Monoclonal Antibodies, Hypomethylating Agents and the Leukemic Microenvironment vol.18, pp.8, 2017, https://doi.org/10.3390/ijms18081660
  14. IL-33 restricts tumor growth and inhibits pulmonary metastasis in melanoma-bearing mice through eosinophils vol.6, pp.6, 2017, https://doi.org/10.1080/2162402X.2017.1317420
  15. The Role of IL-33-Dependent Inflammation in the Tumor Microenvironment vol.7, pp.1664-3224, 2017, https://doi.org/10.3389/fimmu.2016.00682
  16. Role of IL-33 expression in oncogenesis and development of human hepatocellular carcinoma vol.12, pp.1, 2016, https://doi.org/10.3892/ol.2016.4622
  17. Interleukin-33 in human gliomas: Expression and prognostic significance vol.12, pp.1, 2016, https://doi.org/10.3892/ol.2016.4626
  18. IL-33 enhances glioma cell migration and invasion by upregulation of MMP2 and MMP9 via the ST2-NF-κB pathway vol.38, pp.4, 2017, https://doi.org/10.3892/or.2017.5926
  19. Expression and Function of IL-33/ST2 Axis in the Central Nervous System Under Normal and Diseased Conditions vol.9, pp.1664-3224, 2018, https://doi.org/10.3389/fimmu.2018.02596
  20. Contribution of IL-33 to the Pathogenesis of Colorectal Cancer vol.8, pp.2234-943X, 2018, https://doi.org/10.3389/fonc.2018.00561
  21. The Role of IL-33/ST2 Pathway in Tumorigenesis vol.19, pp.9, 2018, https://doi.org/10.3390/ijms19092676
  22. IL-33 facilitates proliferation of colorectal cancer dependent on COX2/PGE2 vol.37, pp.1, 2018, https://doi.org/10.1186/s13046-018-0839-7
  23. pathway and risk of osteosarcoma vol.22, pp.8, 2018, https://doi.org/10.1111/jcmm.13653
  24. Plasma levels of interleukin-33 and soluble suppression of tumorigenicity 2 in patients with advanced pancreatic ductal adenocarcinoma undergoing systemic chemotherapy vol.36, pp.1, 2019, https://doi.org/10.1007/s12032-018-1223-3
  25. Tobacco smoke induced hepatic cancer stem cell-like properties through IL-33/p38 pathway vol.38, pp.1, 2019, https://doi.org/10.1186/s13046-019-1052-z