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dc.contributor.author | Jantus Lewintre, Eloisa | es_ES |
dc.date.accessioned | 2017-01-16T13:59:28Z | |
dc.date.available | 2017-01-16T13:59:28Z | |
dc.date.issued | 2013 | |
dc.identifier.issn | 0027-8874 | |
dc.identifier.uri | http://hdl.handle.net/10251/76886 | |
dc.description | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776260/ | es_ES |
dc.description.abstract | [EN] Background There is a medical need for diagnostic biomarkers in lung cancer. We evaluated the diagnostic performance of complement activation fragments. Methods We assessed complement activation in four bronchial epithelial and seven lung cancer cell lines. C4d, a degradation product of complement activation, was determined in 90 primary lung tumors; bronchoalveolar lavage supernatants from patients with lung cancer (n = 50) and nonmalignant respiratory diseases (n = 22); and plasma samples from advanced (n = 50) and early lung cancer patients (n = 84) subjects with inflammatory lung diseases (n = 133), and asymptomatic individuals enrolled in a lung cancer computed tomography screening program (n = 190). Two-sided P values were calculated by Mann-Whitney U test. Results Lung cancer cells activated the classical complement pathway mediated by C1q binding that was inhibited by phosphomonoesters. Survival was decreased in patients with high C4d deposition in tumors (hazard ratio [HR] = 3.06; 95% confidence interval [CI] = 1.18 to 7.91). C4d levels were increased in bronchoalveolar lavage fluid from lung cancer patients compared with patients with nonmalignant respiratory diseases (0.61 +/- 0.87 vs 0.16 +/- 0.11 mu g/mL; P < .001). C4d levels in plasma samples from lung cancer patients at both advanced and early stages were also increased compared with control subjects (4.13 +/- 2.02 vs 1.86 +/- 0.95 mu g/mL, P < 0.001; 3.18 +/- 3.20 vs 1.13 +/- 0.69 mu g/mL, P < .001, respectively). C4d plasma levels were associated with shorter survival in patients at advanced (HR = 1.59; 95% CI = 0.97 to 2.60) and early stages (HR = 5.57; 95% CI = 1.60 to 19.39). Plasma C4d levels were reduced after surgical removal of lung tumors (P < .001) and were associated with increased lung cancer risk in asymptomatic individuals with (n = 32) or without lung cancer (n = 158) (odds ratio = 4.38; 95% CI = 1.61 to 11.93). Conclusions Complement fragment C4d may serve as a biomarker for early diagnosis and prognosis of lung cancer. | es_ES |
dc.description.sponsorship | This work was supported by UTE project CIMA; the Spanish Government (grant numbers ISCIII-RTICC RD06/0020/0066, RD06/0020/1024, RD12/0036/0025, RD12/0036/0040, RD12/0036/0062, PI08/0923, PI10/01652, PI10/00166, and PI11/00618); the European Regional Development Fund; the European Community’s Seventh Framework Programme (HEALTH-F2-2010-258677- CURELUNG); and the Early Detection Research Network from the National Cancer Institute (grant number U01 CA152662). This work was supported (in part) by a grant (RD12/0036/XXXX) from Red Temática de Investigación Cooperativa en Cáncer, Instituto de Salud Carlos III, Spanish Ministry of Economy and Competitiveness & European Regional Development Fund “Una manera de hacer Europa”. | |
dc.language | Inglés | es_ES |
dc.publisher | Oxford University Press (OUP) | es_ES |
dc.relation.ispartof | JNCI: Journal of the National Cancer Institute | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject | Lung cancer | es_ES |
dc.subject | Factor-h | es_ES |
dc.subject | Immune-response | es_ES |
dc.subject | Cells | es_ES |
dc.subject | Inhibition | es_ES |
dc.subject | Expression | es_ES |
dc.subject | Pathway | es_ES |
dc.subject | System | es_ES |
dc.subject | Confer | es_ES |
dc.subject | C1Q | es_ES |
dc.subject | Diagnosis | es_ES |
dc.subject.classification | MICROBIOLOGIA | es_ES |
dc.title | Investigation of Complement Activation Product C4d as a Diagnostic and Prognostic Biomarker for Lung Cancer | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1093/jnci/djt205 | |
dc.relation.projectID | info:eu-repo/grantAgreement/EC/FP7/258677/EU/Determining (epi)genetic therapeutic signatures for improving lung cancer prognosis/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MSC//RD06%2F0020%2F0066/ES/RED TEMÁTICA DE INVESTIGACIÓN COOPERATIVA DEL CANCER/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MSC//RD06%2F0020%2F1024/ES/RED TEMÁTICA DE INVESTIGACIÓN COOPERATIVA DEL CANCER/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/NIH/NATIONAL CANCER INSTITUTE/5U01CA152662-05/US/ | |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//RD12%2F0036%2F0025/ES/Cáncer/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//RD12%2F0036%2F0040/ES/Cáncer/ | |
dc.relation.projectID | info:eu-repo/grantAgreement/MINECO//RD12%2F0036%2F0062/ES/Cáncer/ | |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//08%2F0923/ES/CONTROL DE LA ACTIVACION DEL COMPLEMENTO SOBRE CELULAS DE CANCER DE PULMON Y SU INFLUENCIA EN EL DESARROLLO TUMORAL/ | |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//PI10%2F01652/ES/ | |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//PI%2F00166/ES/CARACTERIZACION MOLECULAR DEL CARCINOMA PULMONAR EN ESTADIOS INICIALES PARA EL DESARROLLO DE BIOMARCADORES EN EL CONTEXTO DE PROTOCOLOS DE CRIBAJE Y DETECCION PRECOZ/ | |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//PI11%2F00618/ES/Papel del sistema del complemento en la progresión tumoral e identificación de marcadores moleculares relacionados su activación/ | |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Escuela Técnica Superior de Ingeniería Agronómica y del Medio Natural - Escola Tècnica Superior d'Enginyeria Agronòmica i del Medi Natural | es_ES |
dc.description.bibliographicCitation | Jantus Lewintre, E. (2013). Investigation of Complement Activation Product C4d as a Diagnostic and Prognostic Biomarker for Lung Cancer. JNCI: Journal of the National Cancer Institute. 105:1385-1393. https://doi.org/10.1093/jnci/djt205 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://dx.doi.org/10.1093/jnci/djt205 | es_ES |
dc.description.upvformatpinicio | 1385 | es_ES |
dc.description.upvformatpfin | 1393 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 105 | es_ES |
dc.relation.senia | 318762 | es_ES |
dc.identifier.eissn | 1460-2105 | |
dc.identifier.pmid | 23940286 | en_EN |
dc.identifier.pmcid | PMC3776260 | en_EN |
dc.contributor.funder | European Commission | |
dc.contributor.funder | Instituto de Salud Carlos III | |
dc.contributor.funder | Ministerio de Economía y Competitividad |