TY - JOUR
T1 - Implication of BIRC5 in asthma pathogenesis
AU - Ungvári, I.
AU - Hadadi, É.
AU - Virág, V.
AU - Bikov, A.
AU - Nagy, A.
AU - Semsei, T.F.
AU - Gálffy, G.
AU - Tamási, L.
AU - Horváth, I.
AU - Szalai, C.
N1 - Cited By :15
Export Date: 20 February 2019
CODEN: INIME
Correspondence Address: Szalai, C.; Heim Pál Children's Hospital, PO Box 66, H-1958, Budapest, Hungary; email: [email protected]
Chemicals/CAS: survivin, 195263-98-0; BIRC5 protein, human; Inhibitor of Apoptosis Proteins; RNA, Messenger
Funding details: Egészségügyi Tudományos Tanács, ETT, 415/2009
Funding details: Országos Tudományos Kutatási Alapprogramok, OTKA, OTKA
Funding details: Országos Tudományos Kutatási Alapprogramok, OTKA, K81941
Funding details: Nemzeti Kutatási és Technológiai Hivatal, NKTH, TECH_08-A1/2-2008-0120
Funding text 1: Hungarian Scientific Research Fund (OTKA) (K81941); Scientific Committee of the Hungarian Ministry of Health (ETT) (415/2009); National Office of Research and Technology (NKTH) (TECH_08-A1/2-2008-0120).
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J., 22, p. 484; Ambrosini, G., Adida, C., Altieri, D.C., A novel antiapoptosis gene, survivin, expressed in cancer and lymphoma (1997) Nat. Med., 3, p. 917; Li, F., Ambrosini, G., Chu, E.Y., Control of apoptosis and mitotic spindle checkpoint by survivin (1998) Nature, 396, p. 580; Tamm, I., Wang, Y., Sausville, E., IAP-family protein survivin inhibits caspase activity and apoptosis induced by Fas (CD95), Bax, caspases, and anticancer drugs (1998) Cancer Res, 58, p. 5315; Ambrosini, G., Adida, C., Sirugo, G., Altieri, D.C., Induction of apoptosis and inhibition of cell proliferation by survivin gene targeting (1998) J. Biol. Chem., 273, p. 11177; Liu, T., Brouha, B., Grossman, D., Rapid induction of mitochondrial events and caspase-independent apoptosis in survivin-targeted melanoma cells (2004) Oncogene, 23, p. 39; Adida, C., Berrebi, D., Peuchmaur, M., Reyes-Mugica, M., Altieri, D.C., Anti-apoptosis gene, survivin, and prognosis of neuroblastoma (1998) Lancet, 351, p. 882; Mita, A.C., Mita, M.M., Nawrocki, S.T., Giles, F.J., Survivin: key regulator of mitosis and apoptosis and novel target for cancer therapeutics (2008) Clin. Cancer Res., 14, p. 5000; Altznauer, F., Martinelli, S., Yousefi, S., Inflammationassociated cell cycle-independent block of apoptosis by survivin in terminally differentiated neutrophils (2004) J. Exp. Med., 199, p. 1343; Vassina, E.M., Yousefi, S., Simon, D., Zwicky, C., Conus, S., Simon, H.U., cIAP-2 and survivin contribute to cytokinemediated delayed eosinophil apoptosis (2006) Eur. J. Immunol., 36, p. 1975; Tolgyesi, G., Molnar, V., Semsei, A.F., Gene expression profiling of experimental asthma reveals a possible role of paraoxonase-1 in the disease (2009) Int. Immunol., 21, p. 967; Tumes, D.J., Connolly, A., Dent, L.A., Expression of survivin in lung eosinophils is associated with pathology in a mouse model of allergic asthma (2009) Int. Immunol., 21, p. 633; Di Valentin, E., Crahay, C., Garbacki, N., New asthma biomarkers: lessons from murine models of acute and chronic asthma (2009) Am. J. Physiol. Lung Cell. Mol. Physiol., 296, pp. L185; Nathan, R.A., Sorkness, C.A., Kosinski, M., Development of the asthma control test: a survey for assessing asthma control (2004) J. Allergy Clin. Immunol., 113, p. 59; Green, R.H., Brightling, C.E., McKenna, S., Asthma exacerbations and sputum eosinophil counts: a randomised controlled trial (2002) Lancet, 360, p. 1715; Jayaram, L., Pizzichini, M.M., Cook, R.J., Determining asthma treatment by monitoring sputum cell counts: effect on exacerbations (2006) Eur. Respir. J., 27, p. 483; Schleich, F.N., Seidel, L., Sele, J., Exhaled nitric oxide thresholds associated with a sputum eosinophil count >/=3% in a cohort of unselected patients with asthma (2010) Thorax, 65, p. 1039; Virchow Jr., J.C., Kroegel, C., Walker, C., Matthys, H., Inflammatory determinants of asthma severity: mediator and cellular changes in bronchoalveolar lavage fluid of patients with severe asthma (1996) J. Allergy Clin. Immunol., 98, pp. S27; Yang, X., Xiong, G., Chen, X., Survivin expression in esophageal cancer: correlation with p. 53 mutations and promoter polymorphism (2009) Dis. Esophagus, 22, p. 223; Han, C.H., Wei, Q., Lu, K.K., Liu, Z., Mills, G.B., Wang, L.E., Polymorphisms in the survivin promoter are associated with age of onset of ovarian cancer (2009) Int. J. Clin. Exp. Med., 2, p. 289; Dixon, A.L., Liang, L., Moffatt, M.F., A genome-wide association study of global gene expression (2007) Nat. Genet., 39, p. 1202; A haplotype map of the human genome (2005) Nature, 437, p. 1299. , The International HapMap Consortium; Krepela, E., Dankova, P., Moravcikova, E., Increased expression of inhibitor of apoptosis proteins, survivin and XIAP, in non-small cell lung carcinoma (2009) Int. J. Oncol., 35, p. 1449; Hmeljak, J., Erculj, N., Dolzan, V., Kern, I., Cor, A., BIRC5 promoter SNPs do not affect nuclear survivin expression and survival of malignant pleural mesothelioma patients (2011) J Cancer Res. Clin. Oncol., 137, p. 1641; Cheng, Z.J., Hu, L.H., Huang, S.J., Correlation of -31G/C polymorphisms of survivin promoter to tumorigenesis of gastric carcinoma (2008) Ai Zheng, 27, p. 258; Srivastava, K., Srivastava, A., Mittal, B., Survivin promoter -31G/C (rs9904341) polymorphism and cancer susceptibility: a meta-analysis (2012) Mol. Biol. Report., 39, p. 1509; Boidot, R., Vegran, F., Jacob, D., The expression of BIRC5 is correlated with loss of specific chromosomal regions in breast carcinomas (2008) Genes Chromosomes Cancer, 47, p. 299
PY - 2012
Y1 - 2012
N2 - In the last few years, it has been recognized that the unbalanced regulation of survival and apoptosis of bronchial inflammatory cells is a key component in the development of asthma. Baculoviral IAP repeat containing 5 (BIRC5) (also known as survivin) is an important anti-apoptotic protein that has been implicated in many cancer types, and recent studies provide evidence for its role in controlling inflammatory disorders as well. Our aim was to investigate at both genetic and transcriptional levels if BIRC5 has an impact on asthma development. We found that induced sputum samples of patients with bronchial asthma contained elevated levels of BIRC5 mRNA compared with healthy subjects and its level was in correlation with sputum eosinophil percentages. Furthermore, in a case-control study examining single nucleotide polymorphisms (SNPs) in the BIRC5 regulatory regions, the minor alleles of rs8073903 and rs8073069 were found to be significantly associated with asthma and especially non-allergic asthma phenotypes, which associations were more prominent among women. Two marker haplotype analyses further strengthen the impact of these two polymorphisms on both asthma and non-allergic asthma. In the female cohort, rs1508147 was also significantly associated with increased risk of non-allergic asthma. Additionally, with linear regression analysis, we showed that rs9904341 was significantly correlated with both absolute and relative serum eosinophil levels. In conclusion, our results suggest that possibly by inhibition of the eosinophil apoptosis, BIRC5 might be an important regulator of the asthmatic processes and we provide some evidence that its effect might be affected by SNPs located in the gene regulatory regions. © The Japanese Society for Immunology. 2012. All rights reserved.
AB - In the last few years, it has been recognized that the unbalanced regulation of survival and apoptosis of bronchial inflammatory cells is a key component in the development of asthma. Baculoviral IAP repeat containing 5 (BIRC5) (also known as survivin) is an important anti-apoptotic protein that has been implicated in many cancer types, and recent studies provide evidence for its role in controlling inflammatory disorders as well. Our aim was to investigate at both genetic and transcriptional levels if BIRC5 has an impact on asthma development. We found that induced sputum samples of patients with bronchial asthma contained elevated levels of BIRC5 mRNA compared with healthy subjects and its level was in correlation with sputum eosinophil percentages. Furthermore, in a case-control study examining single nucleotide polymorphisms (SNPs) in the BIRC5 regulatory regions, the minor alleles of rs8073903 and rs8073069 were found to be significantly associated with asthma and especially non-allergic asthma phenotypes, which associations were more prominent among women. Two marker haplotype analyses further strengthen the impact of these two polymorphisms on both asthma and non-allergic asthma. In the female cohort, rs1508147 was also significantly associated with increased risk of non-allergic asthma. Additionally, with linear regression analysis, we showed that rs9904341 was significantly correlated with both absolute and relative serum eosinophil levels. In conclusion, our results suggest that possibly by inhibition of the eosinophil apoptosis, BIRC5 might be an important regulator of the asthmatic processes and we provide some evidence that its effect might be affected by SNPs located in the gene regulatory regions. © The Japanese Society for Immunology. 2012. All rights reserved.
KW - Apoptosis
KW - Expression
KW - mRNA
KW - Non-allergic asthma
KW - SNP
KW - Survivin
KW - biological marker
KW - messenger RNA
KW - survivin
KW - adult
KW - allele
KW - apoptosis
KW - article
KW - asthma
KW - Birc5 gene
KW - bronchus
KW - cell survival
KW - cohort analysis
KW - controlled study
KW - eosinophil
KW - female
KW - gene
KW - gene location
KW - genetic transcription
KW - genetic variability
KW - haplotype
KW - human
KW - inflammatory cell
KW - major clinical study
KW - male
KW - pathogenesis
KW - phenotype
KW - priority journal
KW - single nucleotide polymorphism
KW - sputum analysis
KW - Adult
KW - Alleles
KW - Asthma
KW - Case-Control Studies
KW - Female
KW - Haplotypes
KW - Humans
KW - Inhibitor of Apoptosis Proteins
KW - Linear Models
KW - Male
KW - Middle Aged
KW - Phenotype
KW - Polymorphism, Single Nucleotide
KW - RNA, Messenger
KW - Young Adult
U2 - 10.1093/intimm/dxs007
DO - 10.1093/intimm/dxs007
M3 - Article
SN - 0953-8178
VL - 24
SP - 293
EP - 301
JO - International immunology
JF - International immunology
IS - 5
ER -