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Abnormal levels of heterogeneous nuclear ribonucleoprotein A2B1 (hnRNPA2B1) in tumour tissue and blood samples from patients diagnosed with lung cancer

Authors :
Martin P. Barr
Emmet O'Brien
Paul Dowling
Damian Pollard
Martin Clynes
Annemarie Larkin
Michael Moriarty
Kathy Gately
Michael Henry
Vincent J. Lynch
Ross K. Morgan
Jo Ballot
Kenneth J. O'Byrne
Paula Meleady
John Crown
Source :
Molecular BioSystems. 11:743-752
Publication Year :
2015
Publisher :
Royal Society of Chemistry (RSC), 2015.

Abstract

Lung cancer is the second most common type of cancer in the world and is the most common cause of cancer-related death in both men and women. Research into causes, prevention and treatment of lung cancer is ongoing and much progress has been made recently in these areas, however survival rates have not significantly improved. Therefore, it is essential to develop biomarkers for early diagnosis of lung cancer, prediction of metastasis and evaluation of treatment efficiency, as well as using these molecules to provide some understanding about tumour biology and translate highly promising findings in basic science research to clinical application. In this investigation, two-dimensional difference gel electrophoresis and mass spectrometry were initially used to analyse conditioned media from a panel of lung cancer and normal bronchial epithelial cell lines. Significant proteins were identified with heterogeneous nuclear ribonucleoprotein A2B1 (hnRNPA2B1), pyruvate kinase M2 isoform (PKM2), Hsc-70 interacting protein and lactate dehydrogenase A (LDHA) selected for analysis in serum from healthy individuals and lung cancer patients. hnRNPA2B1, PKM2 and LDHA were found to be statistically significant in all comparisons. Tissue analysis and knockdown of hnRNPA2B1 using siRNA subsequently demonstrated both the overexpression and potential role for this molecule in lung tumorigenesis. The data presented highlights a number of in vitro derived candidate biomarkers subsequently verified in patient samples and also provides some insight into their roles in the complex intracellular mechanisms associated with tumour progression.

Details

ISSN :
17422051 and 1742206X
Volume :
11
Database :
OpenAIRE
Journal :
Molecular BioSystems
Accession number :
edsair.doi.dedup.....c60d93a26969a78bc2cdceef531d7160