Gene expression signature of non-involved lung tissue associated with survival in lung adenocarcinoma patients.

Lung adenocarcinoma patients of similar clinical stage and undergoing the same treatments often have marked interindividual variations in prognosis. These clinical discrepancies may be due to the genetic background modulating an individual's predisposition to fighting cancer. Herein, we hypothesized that the lung microenvironment, as reflected by its expression profile, may affect lung adenocarcinoma patients' survival. The transcriptome of non-involved lung tissue, excised from a discovery series of 204 lung adenocarcinoma patients, was evaluated using whole-genome expression microarrays (with probes corresponding to 28 688 well-annotated coding sequences). Genes associated with survival status at 60 months were identified by Cox regression analysis (adjusted for gender, age and clinical stage) and retested in a validation series of 78 additional cases. RNA-Seq analysis from non-involved lung tissue of 12 patients was performed to characterize the different isoforms of candidate genes. Ten genes for which the loge-transformed hazard ratios expressed the same direction of effect in the discovery (P < 1.0 × 10(-3)) and validation series comprised the gene expression signature associated with survival: CNTNAP1, PKNOX1, FAM156A, FRMD8, GALNTL1, TXNDC12, SNTB1, PPP3R1, SNX10 and SERPINH1. RNA sequencing highlighted the complex expression pattern of these genes in non-involved lung tissue from different patients and permitted the detection of a read-through gene fusion between PPP3R1 and the flanking gene (CNRIP1) as well as a novel isoform of CNTNAP1. Our findings support the hypothesis that individual genetic characteristics, evidenced by the expression pattern of non-involved tissue, influence the outcome of lung adenocarcinoma patients.

[1]  Tao Wang,et al.  FERM‐containing protein FRMD5 is a p120‐catenin interacting protein that regulates tumor progression , 2012, FEBS letters.

[2]  Ugo Pastorino,et al.  Association of lung adenocarcinoma clinical stage with gene expression pattern in noninvolved lung tissue , 2012, International journal of cancer.

[3]  Po-Huang Lee,et al.  Mucin glycosylating enzyme GALNT2 regulates the malignant character of hepatocellular carcinoma by modifying the EGF receptor. , 2011, Cancer research.

[4]  Pengyuan Liu,et al.  Gene-Expression Signature Predicts Postoperative Recurrence in Stage I Non-Small Cell Lung Cancer Patients , 2012, PloS one.

[5]  David E. Misek,et al.  Gene-expression profiles predict survival of patients with lung adenocarcinoma , 2002, Nature Medicine.

[6]  Gang Liu,et al.  Effects of cigarette smoke on the human airway epithelial cell transcriptome. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[7]  E. E. Vincent,et al.  Overexpression of the TXNDC5 protein in non-small cell lung carcinoma. , 2011, Anticancer research.

[8]  P. Nuciforo,et al.  Prep1 (pKnox1)‐deficiency leads to spontaneous tumor development in mice and accelerates EμMyc lymphomagenesis: A tumor suppressor role for Prep1 , 2010, Molecular oncology.

[9]  T. Dragani,et al.  Multigenic nature of the mouse pulmonary adenoma progression 1 locus , 2013, BMC Genomics.

[10]  M. McCarthy,et al.  Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes , 2008, Nature Genetics.

[11]  Igor Jurisica,et al.  Gene expression–based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study , 2008, Nature Medicine.

[12]  Humam Kadara,et al.  Field cancerization in non-small cell lung cancer: implications in disease pathogenesis. , 2012, Proceedings of the American Thoracic Society.

[13]  K. Mossman The Wellcome Trust Case Control Consortium, U.K. , 2008 .

[14]  M. Zheng,et al.  TXNDC9 Expression in Colorectal Cancer Cells and Its Influence on Colorectal Cancer Prognosis , 2012, Cancer investigation.

[15]  L. Morse,et al.  SNX10 is required for osteoclast formation and resorption activity , 2012, Journal of cellular biochemistry.

[16]  Helga Thorvaldsdóttir,et al.  Integrative Genomics Viewer , 2011, Nature Biotechnology.

[17]  Keitaro Matsuo,et al.  Relapse-related molecular signature in lung adenocarcinomas identifies patients with dismal prognosis. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[18]  F. Watt,et al.  FRMD4A upregulation in human squamous cell carcinoma promotes tumor growth and metastasis and is associated with poor prognosis. , 2012, Cancer research.

[19]  I. Wistuba,et al.  Pulmonary adenocarcinoma: A renewed entity in 2011 , 2012, Respirology.

[20]  S L Normand,et al.  Meta-analysis: formulating, evaluating, combining, and reporting. , 1999, Statistics in medicine.

[21]  Lior Pachter,et al.  Sequence Analysis , 2020, Definitions.

[22]  A. Nicholson,et al.  Non-small-cell lung cancer , 2011, The Lancet.

[23]  J. Marin,et al.  Genetic variants in genes involved in mechanisms of chemoresistance to anticancer drugs. , 2012, Current cancer drug targets.

[24]  G. Crabtree,et al.  Neonatal β cell development in mice and humans is regulated by calcineurin/NFAT. , 2012, Developmental cell.

[25]  Pan Du,et al.  lumi: a pipeline for processing Illumina microarray , 2008, Bioinform..

[26]  A. Schulz,et al.  SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity , 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[27]  Lude Franke,et al.  eQTL analysis in humans. , 2009, Methods in molecular biology.

[28]  Michael A. Freitas,et al.  Proteomic Analysis Reveals New Cardiac-Specific Dystrophin-Associated Proteins , 2012, PloS one.

[29]  M. Mine,et al.  Serum heat shock protein 47 levels are elevated in acute exacerbation of idiopathic pulmonary fibrosis , 2013, Cell Stress and Chaperones.

[30]  J. Pignon,et al.  Impact of Systematic EGFR and KRAS Mutation Evaluation on Progression-Free Survival and Overall Survival in Patients with Advanced Non–Small-Cell Lung Cancer Treated by Erlotinib in a French Prospective Cohort (ERMETIC Project—Part 2) , 2012, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

[31]  Yoo Jin Jung,et al.  The transcriptional landscape and mutational profile of lung adenocarcinoma , 2012, Genome research.

[32]  G. Iotti,et al.  Homeodomain transcription factor and tumor suppressor Prep1 is required to maintain genomic stability , 2011, Proceedings of the National Academy of Sciences.

[33]  D. Bers,et al.  Impaired contractile function and calcium handling in hearts of cardiac-specific calcineurin b1-deficient mice. , 2009, American journal of physiology. Heart and circulatory physiology.

[34]  K. Nagata,et al.  Hsp47 as a collagen-specific molecular chaperone. , 2011, Methods in enzymology.

[35]  M. Ladanyi,et al.  Association of KRAS and EGFR mutations with survival in patients with advanced lung adenocarcinomas , 2013, Cancer.

[36]  Eun Sung Park,et al.  Development and Validation of a Prognostic Gene-Expression Signature for Lung Adenocarcinoma , 2012, PloS one.

[37]  David C Christiani,et al.  Genome-wide analysis of survival in early-stage non-small-cell lung cancer. , 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[38]  D. Nie,et al.  Abstract 3424: Cancer cells lose their expression of lipoxygenases in order to activate pro-survival and angiogenic pathways thereby establishing successful macro-metastases , 2012 .

[39]  Jean YH Yang,et al.  Bioconductor: open software development for computational biology and bioinformatics , 2004, Genome Biology.

[40]  Kyong-Ah Yoon,et al.  Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study. , 2013, Carcinogenesis.

[41]  A. González-Neira,et al.  Multiple Genetic Loci Modulate Lung Adenocarcinoma Clinical Staging , 2011, Clinical Cancer Research.