Integrative Analyses Identify Osteopontin, LAMB3 and ITGB1 as Critical Pro-Metastatic Genes for Lung Cancer

Objective To explore the key regulatory genes associated with lung cancer in order to reduce its occurrence and progress through silencing these key genes. Methods To identify the key regulatory genes involved in lung cancer, we performed a combination of gene array and bioinformatics analyses to compare gene transcription profiles in 3 monoclonal cell strains with high, medium or low metastatic abilities, which were separated from the SPC-A-1sci and SPC-A-1 cell lines by limiting dilution monoclone assay. We then analyzed those genes’ biological activities by knocking down their expression in SPC-A-1sci cells using siRNA and lenti-viral shRNA vectors, followed by determinations of the invasion and migration capabilities of the resulting cell lines in vitro as well as their potential for inducing occurrence and metastasis of lung cancer in vivo. To examine the clinical relevance of these findings, we analyzed the expression levels of the identified genes in human lung cancer tissues (n = 135) and matched adjacent normal tissues by immunohistochemical (IHC) staining. Results Three monoclonal cell strains characterized with high, medium or low metastatic abilities were successfully selected. Gene array and bioinformatics analyses implied that osteopontin, LAMB3 and ITGB1 were key genes involved in lung cancer. Knockdown of these genes suppressed human lung cancer cell invasion and metastasis in vitro and in vivo. Clinical sample analyses indicated that osteopontin, LAMB3 and ITGB1 protein expression levels were higher in lung cancer patients, compared to non-cancerous adjacent tissues, and correlated with lymphatic metastasis. Conclusions We confirmed that osteopontin, LAMB3 and ITGB1 played important roles in the occurrence and metastasis of lung cancer, thus provided important clues to understanding the molecular mechanism of metastasis and contributing to the therapeutic treatment of lung cancer.

[1]  Shanthi M. Colaco,et al.  Anti-laminin-332 mucous membrane pemphigoid associated with recurrent metastatic prostate carcinoma: hypothesis for a paraneoplastic phenomenon. , 2011, European journal of dermatology : EJD.

[2]  F. Tsai,et al.  Osteopontin increases lung cancer cells migration via activation of the alphavbeta3 integrin/FAK/Akt and NF-kappaB-dependent pathway. , 2009, Lung cancer.

[3]  Robert A. Weinberg,et al.  Tumor Metastasis: Molecular Insights and Evolving Paradigms , 2011, Cell.

[4]  Lei Liu,et al.  Development of a highly metastatic model that reveals a crucial role of fibronectin in lung cancer cell migration and invasion , 2010, BMC Cancer.

[5]  R. Nagle,et al.  Laminin-5 beta3A expression in LNCaP human prostate carcinoma cells increases cell migration and tumorigenicity. , 2004, Neoplasia.

[6]  Alexander Nyström,et al.  Laminin isoforms in development and disease , 2007, Journal of Molecular Medicine.

[7]  C. DiPersio,et al.  Integrin α3β1 as a breast cancer target , 2011, Expert opinion on therapeutic targets.

[8]  Albert-László Barabási,et al.  Genome-scale analysis of in vivo spatiotemporal promoter activity in Caenorhabditis elegans , 2007, Nature Biotechnology.

[9]  R. Eils,et al.  Gene network dynamics controlling keratinocyte migration , 2008, Molecular systems biology.

[10]  L. Tanoue Cancer Statistics, 2009 , 2010 .

[11]  Hao Wang,et al.  A humanized anti-osteopontin antibody inhibits breast cancer growth and metastasis in vivo , 2010, Cancer Immunology, Immunotherapy.

[12]  Ardeshir Bayat,et al.  Degenerate Wave and Capacitive Coupling Increase Human MSC Invasion and Proliferation While Reducing Cytotoxicity in an In Vitro Wound Healing Model , 2011, PloS one.

[13]  蔡輔仁,et al.  Osteopontin increases lung cancer cells migration via activation of the αvβ3 integrin/FAK/Akt and NF-kB-dependent pathway , 2009 .

[14]  V. Quaranta,et al.  Laminin-332 Is a Substrate for Hepsin, a Protease Associated with Prostate Cancer Progression* , 2008, Journal of Biological Chemistry.

[15]  Guofeng Zhang,et al.  Lentviral-mediated RNAi to inhibit target gene expression of the porcine integrin αv subunit, the FMDV receptor, and against FMDV infection in PK-15 cells , 2011, Virology Journal.

[16]  D. Lin,et al.  Overexpression of Osteopontin Is Associated with More Aggressive Phenotypes in Human Non–Small Cell Lung Cancer , 2005, Clinical Cancer Research.

[17]  J. Rogers,et al.  Coping with cold: An integrative, multitissue analysis of the transcriptome of a poikilothermic vertebrate. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[18]  R. Kerbel,et al.  Development of a preclinical model of spontaneous human melanoma central nervous system metastasis. , 2008, Cancer research.

[19]  D. Tarin Clinical and Biological Implications of the Tumor Microenvironment , 2012, Cancer Microenvironment.

[20]  Hiroyuki Yamamoto,et al.  Co-expression of laminin β3 and γ2 chains and epigenetic inactivation of laminin α3 chain in gastric cancer. , 2011, International journal of oncology.

[21]  Guoxin Zhang,et al.  Osteopontin Enhances the Expression and Activity of MMP-2 via the SDF-1/CXCR4 Axis in Hepatocellular Carcinoma Cell Lines , 2011, PloS one.

[22]  D. Nguyen Tracing the origins of metastasis , 2011, The Journal of pathology.

[23]  P. simon-Assmann,et al.  Role of laminins in physiological and pathological angiogenesis. , 2011, The International journal of developmental biology.

[24]  Takako Sasaki,et al.  Melanoma cells produce multiple laminin isoforms and strongly migrate on α5 laminin(s) via several integrin receptors. , 2011, Experimental cell research.

[25]  Susanna M Cramb,et al.  The International Epidemiology of Lung Cancer: Geographical Distribution and Secular Trends , 2008, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

[26]  I. Han,et al.  Keratinocyte-derived Laminin-332 Promotes Adhesion and Migration in Melanocytes and Melanoma* , 2011, The Journal of Biological Chemistry.

[27]  A. Jemal,et al.  Global cancer statistics , 2011, CA: a cancer journal for clinicians.

[28]  Y. Ohe,et al.  Abrogation of the interaction between osteopontin and αvβ3 integrin reduces tumor growth of human lung cancer cells in mice , 2007 .

[29]  A. Jemal,et al.  Global Cancer Statistics , 2011 .

[30]  K. Syrigos,et al.  Cell Adhesion Molecules: Role and Clinical Significance in Cancer , 2009, Cancer investigation.

[31]  M. El-Tanani Role of osteopontin in cellular signaling and metastatic phenotype. , 2008, Frontiers in bioscience : a journal and virtual library.

[32]  Susumu Goto,et al.  The KEGG resource for deciphering the genome , 2004, Nucleic Acids Res..

[33]  T. Okada,et al.  A highly bone marrow metastatic murine breast cancer model established through in vivo selection exhibits enhanced anchorage-independent growth and cell migration mediated by ICAM-1 , 2008, Clinical & Experimental Metastasis.

[34]  A. Jemal,et al.  Cancer Statistics, 2009 , 2009, CA: a cancer journal for clinicians.

[35]  Ming Yi,et al.  WholePathwayScope: a comprehensive pathway-based analysis tool for high-throughput data , 2006, BMC Bioinformatics.

[36]  P. Khatri,et al.  A systems biology approach for pathway level analysis. , 2007, Genome research.

[37]  Ben Fabry,et al.  Contractile forces in tumor cell migration. , 2008, European journal of cell biology.

[38]  Klaus Pantel,et al.  Circulating tumour cells in cancer patients: challenges and perspectives. , 2010, Trends in molecular medicine.

[39]  A. Koong,et al.  The RGD Domain of Human Osteopontin Promotes Tumor Growth and Metastasis through Activation of Survival Pathways , 2010, PloS one.

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

[41]  Michael Lappe,et al.  From gene networks to gene function. , 2003, Genome research.

[42]  N. Dubrawsky Cancer statistics , 1989, CA: a cancer journal for clinicians.

[43]  G. Fontanini,et al.  Osteopontin Expression and Prognostic Significance in Non–Small Cell Lung Cancer , 2005, Clinical Cancer Research.

[44]  P. Johnston,et al.  Agelastatin A: a novel inhibitor of osteopontin-mediated adhesion, invasion, and colony formation , 2008, Molecular Cancer Therapeutics.