Pathways affected by asbestos exposure in normal and tumour tissue of lung cancer patients

BackgroundStudies on asbestos-induced tumourigenesis have indicated the role of, e.g., reactive oxygen/nitrogen species, mitochondria, as well as NF-κB and MAPK signalling pathways. The exact molecular mechanisms contributing to asbestos-mediated carcinogenesis are, however, still to be characterized.MethodsIn this study, gene expression data analyses together with gene annotation data from the Gene Ontology (GO) database were utilized to identify pathways that are differentially regulated in lung and tumour tissues between asbestos-exposed and non-exposed lung cancer patients. Differentially regulated pathways were identified from gene expression data from 14 asbestos-exposed and 14 non-exposed lung cancer patients using custom-made software and Iterative Group Analysis (iGA). Western blotting was used to further characterize the findings, specifically to determine the protein levels of UBA1 and UBA7.ResultsDifferences between asbestos-related and non-related lung tumours were detected in pathways associated with, e.g., ion transport, NF-κB signalling, DNA repair, as well as spliceosome and nucleosome complexes. A notable fraction of the pathways down-regulated in both normal and tumour tissue of the asbestos-exposed patients were related to protein ubiquitination, a versatile process regulating, for instance, DNA repair, cell cycle, and apoptosis, and thus being also a significant contributor of carcinogenesis. Even though UBA1 or UBA7, the early enzymes involved in protein ubiquitination and ubiquitin-like regulation of target proteins, did not underlie the exposure-related deregulation of ubiquitination, a difference was detected in the UBA1 and UBA7 levels between squamous cell carcinomas and respective normal lung tissue (p = 0.02 and p = 0.01) without regard to exposure status.ConclusionOur results indicate alterations in protein ubiquitination related both to cancer type and asbestos. We present for the first time pathway analysis results on asbestos-associated lung cancer, providing important insight into the most relevant targets for future research.

[1]  M. Djamgoz,et al.  Voltage-gated Na+ channels: multiplicity of expression, plasticity, functional implications and pathophysiological aspects , 2004, European Biophysics Journal.

[2]  S. Anttila,et al.  Asbestos exposure among Finnish lung cancer patients: occupational history and fiber concentration in lung tissue. , 1993, American journal of industrial medicine.

[3]  J. Osinga,et al.  A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer. , 1992, Cancer research.

[4]  M. Ashburner,et al.  Gene Ontology: tool for the unification of biology , 2000, Nature Genetics.

[5]  R. Krug,et al.  The UbcH8 ubiquitin E2 enzyme is also the E2 enzyme for ISG15, an IFN-α/β-induced ubiquitin-like protein , 2004 .

[6]  Ivan Dikic,et al.  Ubiquitylation and cell signaling , 2005, The EMBO journal.

[7]  A. Churg Lung cancer cell type and asbestos exposure. , 1985, JAMA.

[8]  S. Anttila,et al.  Asbestos exposure and the risk of lung cancer in a general urban population. , 1994, Scandinavian journal of work, environment & health.

[9]  F. Sánchez-Jiménez,et al.  Role of reactive oxygen species in apoptosis: implications for cancer therapy. , 2000, The international journal of biochemistry & cell biology.

[10]  Sarah J. Roberts-Thomson,et al.  Calcium and cancer: targeting Ca2+ transport , 2007, Nature Reviews Cancer.

[11]  J. Barrett,et al.  Induction by asbestos fibers of anaphase abnormalities: mechanism for aneuploidy induction and possibly carcinogenesis. , 1985, Carcinogenesis.

[12]  K. Aldape,et al.  Loss of Heterozygosity of Chromosome 3p21 Is Associated with Mutant TP53 and Better Patient Survival in Non–Small-Cell Lung Cancer , 2004, Cancer Research.

[13]  F. Lehmann-Horn,et al.  Human muscle voltage-gated ion channels and hereditary disease. , 2001, Current opinion in pharmacology.

[14]  Rainer Breitling,et al.  Iterative Group Analysis (iGA): A simple tool to enhance sensitivity and facilitate interpretation of microarray experiments , 2004, BMC Bioinformatics.

[15]  Rafael A. Irizarry,et al.  A Model-Based Background Adjustment for Oligonucleotide Expression Arrays , 2004 .

[16]  B. Mossman,et al.  Cell signaling pathways elicited by asbestos. , 1997, Environmental health perspectives.

[17]  Steven J. Sollott,et al.  Reactive Oxygen Species (Ros-Induced) Ros Release , 2000, The Journal of experimental medicine.

[18]  M. Hobbs,et al.  Exposure to crocidolite and the incidence of different histological types of lung cancer. , 1996, Occupational and environmental medicine.

[19]  T. Kauppinen,et al.  Incidence of cancer among Finnish patients with asbestos-related pulmonary or pleural fibrosis , 1999, Cancer Causes & Control.

[20]  Daniela Hoeller,et al.  Ubiquitin and ubiquitin-like proteins in cancer pathogenesis , 2006, Nature Reviews Cancer.

[21]  S. Weitzman,et al.  The mitochondria-regulated death pathway mediates asbestos-induced alveolar epithelial cell apoptosis. , 2003, American journal of respiratory cell and molecular biology.

[22]  Gene Ontology Consortium,et al.  The Gene Ontology (GO) project in 2006 , 2005, Nucleic Acids Res..

[23]  Zhandong Liu,et al.  Role of Ubiquitin-proteasome proteolytic pathway in malignant pleural mesothelioma. , 2007 .

[24]  D. Kamp,et al.  Asbestos-Induced Pulmonary Toxicity: Role of DNA Damage and Apoptosis , 2003, Experimental biology and medicine.

[25]  P. C. Viswanathan,et al.  Inherited sodium channelopathies: a continuum of channel dysfunction. , 2004, Trends in cardiovascular medicine.

[26]  J. Cidlowski,et al.  Molecular interplay between ion channels and the regulation of apoptosis. , 2002, Biological research.

[27]  S. Reddy,et al.  Oxidants and signaling by mitogen-activated protein kinases in lung epithelium. , 2006, American journal of respiratory cell and molecular biology.

[28]  Samuel Kaski,et al.  Gene expression profiles in asbestos-exposed epithelial and mesothelial lung cell lines , 2007, BMC Genomics.

[29]  F. Lang,et al.  Ion Channels in Cell Proliferation and Apoptotic Cell Death , 2005, The Journal of Membrane Biology.

[30]  S. Knuutila,et al.  Identification of specific gene copy number changes in asbestos-related lung cancer. , 2006, Cancer research.

[31]  S. Knuutila,et al.  Gene expression and copy number profiling suggests the importance of allelic imbalance in 19p in asbestos-associated lung cancer , 2007, Oncogene.

[32]  R. Coombes,et al.  Voltage-Gated Sodium Channel Expression and Potentiation of Human Breast Cancer Metastasis , 2005, Clinical Cancer Research.

[33]  H. Yokosawa,et al.  Link between the ubiquitin conjugation system and the ISG15 conjugation system: ISG15 conjugation to the UbcH6 ubiquitin E2 enzyme. , 2005, Journal of biochemistry.

[34]  B. Mossman,et al.  Asbestos causes translocation of p65 protein and increases NF-kappa B DNA binding activity in rat lung epithelial and pleural mesothelial cells. , 1997, The American journal of pathology.

[35]  X. Baur,et al.  Increased Incidence of DNA Double-strand Breaks and Anti-ds DNA Antibodies in Blood of Workers Occupationally Exposed to Asbestos , 1994, Human & experimental toxicology.

[36]  P Boffetta,et al.  Mechanisms of the combined effect of asbestos and smoking in the etiology of lung cancer. , 1994, Scandinavian journal of work, environment & health.

[37]  T. Kraus,et al.  Levels of 8-hydroxy-2'-deoxyguanosine in DNA of white blood cells from workers highly exposed to asbestos in Germany. , 2000, Mutation research.

[38]  A. Borczuk,et al.  Molecular profiling of malignant peritoneal mesothelioma identifies the ubiquitin-proteasome pathway as a therapeutic target in poor prognosis tumors. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[39]  R. Krug,et al.  The UbcH8 ubiquitin E2 enzyme is also the E2 enzyme for ISG15, an IFN-alpha/beta-induced ubiquitin-like protein. , 2004, Proceedings of the National Academy of Sciences of the United States of America.