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báo cáo hóa học: Identification of a biomarker panel using a multiplex proximity ligation assay improves accuracy of pancreatic cancer diagnosis
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Tuyển tập các báo cáo nghiên cứu về hóa học được đăng trên tạp chí sinh học quốc tế đề tài : Identification of a biomarker panel using a multiplex proximity ligation assay improves accuracy of pancreatic cancer diagnosis
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báo cáo hóa học:" Identification of a biomarker panel using a multiplex proximity ligation assay improves accuracy of pancreatic cancer diagnosis"Journal of Translational Medicine BioMed Central Open AccessResearchIdentification of a biomarker panel using a multiplex proximityligation assay improves accuracy of pancreatic cancer diagnosisStephanie T Chang†1, Jacob M Zahn†2,3, Joe Horecka2,3, Pamela L Kunz5,James M Ford4,5, George A Fisher5, Quynh T Le1, Daniel T Chang1,Hanlee Ji2,5 and Albert C Koong*1Address: 1Department of Radiation Oncology, Stanford University School of Medicine, Stanford University, Stanford, CA, USA, 2Stanford GenomeTechnology Center, Stanford University School of Medicine, Stanford University, Stanford, CA, USA, 3Department of Biochemistry, StanfordUniversity School of Medicine, Stanford University, Stanford, CA, USA, 4Department of Genetics, Stanford University School of Medicine, StanfordUniversity, Stanford, CA, USA and 5Department of Medicine, Division of Medical Oncology, Stanford University School of Medicine, StanfordUniversity, Stanford, CA, USAEmail: Stephanie T Chang - stephanietchang@gmail.com; Jacob M Zahn - jzahn@stanford.edu; Joe Horecka - jhorecka@stanford.edu;Pamela L Kunz - pkunz@stanford.edu; James M Ford - jmf@stanford.edu; George A Fisher - georgeaf@stanford.edu;Quynh T Le - qle@stanford.edu; Daniel T Chang - dtchang@stanford.edu; Hanlee Ji - genomics_ji@stanford.edu;Albert C Koong* - akoong@stanford.edu* Corresponding author †Equal contributorsPublished: 11 December 2009 Received: 5 September 2009 Accepted: 11 December 2009Journal of Translational Medicine 2009, 7:105 doi:10.1186/1479-5876-7-105This article is available from: http://www.translational-medicine.com/content/7/1/105© 2009 Chang et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Pancreatic cancer continues to prove difficult to clinically diagnose. Multiple simultaneous measurements of plasma biomarkers can increase sensitivity and selectivity of diagnosis. Proximity ligation assay (PLA) is a highly sensitive technique for multiplex detection of biomarkers in plasma with little or no interfering background signal. Methods: We examined the plasma levels of 21 biomarkers in a clinically defined cohort of 52 locally advanced (Stage II/III) pancreatic ductal adenocarcinoma cases and 43 age-matched controls using a multiplex proximity ligation assay. The optimal biomarker panel for diagnosis was computed using a combination of the PAM algorithm and logistic regression modeling. Biomarkers that were significantly prognostic for survival in combination were determined using univariate and multivariate Cox survival models. Results: Three markers, CA19-9, OPN and CHI3L1, measured in multiplex were found to have superior sensitivity for pancreatic cancer vs. CA19-9 alone (93% vs. 80%). In addition, we identified two markers, CEA and CA125, that when measured simultaneously have prognostic significance for survival for this clinical stage of pancreatic cancer (p < 0.003). Conclusions: A multiplex panel assaying CA19-9, OPN and CHI3L1 in plasma improves accuracy of pancreatic cancer diagnosis. A panel assaying CEA and CA125 in plasma can predict survival for this clinical cohort of pancreatic cancer patients. Page 1 of 12 (page number not for citation purposes)Journal of Translational Medicine 2009, 7:105 http://www.translational-medicine.com/content/7/1/105 kers for pancreatic cancer [6,7]. PLA was initially devel-BackgroundIn 2008, the incidence of pancreatic cancer in the United oped as a technique to improve the sensitivity ...
Nội dung trích xuất từ tài liệu:
báo cáo hóa học:" Identification of a biomarker panel using a multiplex proximity ligation assay improves accuracy of pancreatic cancer diagnosis"Journal of Translational Medicine BioMed Central Open AccessResearchIdentification of a biomarker panel using a multiplex proximityligation assay improves accuracy of pancreatic cancer diagnosisStephanie T Chang†1, Jacob M Zahn†2,3, Joe Horecka2,3, Pamela L Kunz5,James M Ford4,5, George A Fisher5, Quynh T Le1, Daniel T Chang1,Hanlee Ji2,5 and Albert C Koong*1Address: 1Department of Radiation Oncology, Stanford University School of Medicine, Stanford University, Stanford, CA, USA, 2Stanford GenomeTechnology Center, Stanford University School of Medicine, Stanford University, Stanford, CA, USA, 3Department of Biochemistry, StanfordUniversity School of Medicine, Stanford University, Stanford, CA, USA, 4Department of Genetics, Stanford University School of Medicine, StanfordUniversity, Stanford, CA, USA and 5Department of Medicine, Division of Medical Oncology, Stanford University School of Medicine, StanfordUniversity, Stanford, CA, USAEmail: Stephanie T Chang - stephanietchang@gmail.com; Jacob M Zahn - jzahn@stanford.edu; Joe Horecka - jhorecka@stanford.edu;Pamela L Kunz - pkunz@stanford.edu; James M Ford - jmf@stanford.edu; George A Fisher - georgeaf@stanford.edu;Quynh T Le - qle@stanford.edu; Daniel T Chang - dtchang@stanford.edu; Hanlee Ji - genomics_ji@stanford.edu;Albert C Koong* - akoong@stanford.edu* Corresponding author †Equal contributorsPublished: 11 December 2009 Received: 5 September 2009 Accepted: 11 December 2009Journal of Translational Medicine 2009, 7:105 doi:10.1186/1479-5876-7-105This article is available from: http://www.translational-medicine.com/content/7/1/105© 2009 Chang et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Pancreatic cancer continues to prove difficult to clinically diagnose. Multiple simultaneous measurements of plasma biomarkers can increase sensitivity and selectivity of diagnosis. Proximity ligation assay (PLA) is a highly sensitive technique for multiplex detection of biomarkers in plasma with little or no interfering background signal. Methods: We examined the plasma levels of 21 biomarkers in a clinically defined cohort of 52 locally advanced (Stage II/III) pancreatic ductal adenocarcinoma cases and 43 age-matched controls using a multiplex proximity ligation assay. The optimal biomarker panel for diagnosis was computed using a combination of the PAM algorithm and logistic regression modeling. Biomarkers that were significantly prognostic for survival in combination were determined using univariate and multivariate Cox survival models. Results: Three markers, CA19-9, OPN and CHI3L1, measured in multiplex were found to have superior sensitivity for pancreatic cancer vs. CA19-9 alone (93% vs. 80%). In addition, we identified two markers, CEA and CA125, that when measured simultaneously have prognostic significance for survival for this clinical stage of pancreatic cancer (p < 0.003). Conclusions: A multiplex panel assaying CA19-9, OPN and CHI3L1 in plasma improves accuracy of pancreatic cancer diagnosis. A panel assaying CEA and CA125 in plasma can predict survival for this clinical cohort of pancreatic cancer patients. Page 1 of 12 (page number not for citation purposes)Journal of Translational Medicine 2009, 7:105 http://www.translational-medicine.com/content/7/1/105 kers for pancreatic cancer [6,7]. PLA was initially devel-BackgroundIn 2008, the incidence of pancreatic cancer in the United oped as a technique to improve the sensitivity ...
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