Lung Cancer Diagnosis from Proteomic Analysis of Preinvasive Lesions
Early detection may help improve survival from lung cancer. In this study, our goal was to derive and validate a signature from the proteomic analysis of bronchial lesions that could predict the diagnosis of lung cancer. Using previously published studies of bronchial tissues, we selected a signatur...
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Published in | Cancer research (Chicago, Ill.) Vol. 71; no. 8; pp. 3009 - 3017 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Philadelphia, PA
American Association for Cancer Research
15.04.2011
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Subjects | |
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Abstract | Early detection may help improve survival from lung cancer. In this study, our goal was to derive and validate a signature from the proteomic analysis of bronchial lesions that could predict the diagnosis of lung cancer. Using previously published studies of bronchial tissues, we selected a signature of nine matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) mass-to-charge ratio features to build a prediction model diagnostic of lung cancer. The model was based on MALDI MS signal intensity (MALDI score) from bronchial tissue specimens from our 2005 published cohort of 51 patients. The performance of the prediction model in identifying lung cancer was tested in an independent cohort of bronchial specimens from 60 patients. The probability of having lung cancer based on the proteomic analysis of the bronchial specimens was characterized by an area under the receiver operating characteristic curve of 0.77 (95% CI 0.66-0.88) in this validation cohort. Eight of the nine features were identified and validated by Western blotting and immunohistochemistry. These results show that proteomic analysis of endobronchial lesions may facilitate the diagnosis of lung cancer and the monitoring of high-risk individuals for lung cancer in surveillance and chemoprevention trials. |
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AbstractList | Early detection may help improve survival from lung cancer. In this study, our goal was to derive and validate a signature from the proteomic analysis of bronchial lesions that could predict the diagnosis of lung cancer. Using previously published studies of bronchial tissues, we selected a signature of nine matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) mass-to-charge ratio features to build a prediction model diagnostic of lung cancer. The model was based on MALDI MS signal intensity (MALDI score) from bronchial tissue specimens from our 2005 published cohort of 51 patients. The performance of the prediction model in identifying lung cancer was tested in an independent cohort of bronchial specimens from 60 patients. The probability of having lung cancer based on the proteomic analysis of the bronchial specimens was characterized by an area under the receiver operating characteristic curve of 0.77 (95% CI 0.66-0.88) in this validation cohort. Eight of the nine features were identified and validated by Western blotting and immunohistochemistry. These results show that proteomic analysis of endobronchial lesions may facilitate the diagnosis of lung cancer and the monitoring of high-risk individuals for lung cancer in surveillance and chemoprevention trials. Early detection may help improve survival from lung cancer. In this study our goal was to derive and validate a signature from the proteomic analysis of bronchial lesions that could predict the diagnosis of lung cancer. Using previously published studies of bronchial tissues we selected a signature of 9 matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) mass to charge ratio features to build a prediction model diagnostic of lung cancer. The model was based on MALDI MS signal intensity (MALDI score) from bronchial tissue specimens from our 2005 published cohort of 51 patients. The performance of the prediction model in identifying lung cancer was tested in an independent cohort of bronchial specimens from 60 patients. The probability of having lung cancer based on the proteomic analysis of the bronchial specimens was characterized by an area under the receiver operating characteristic curve of 0.77 (95% CI 0.66 to 0.88) in this validation cohort. Eight of the 9 features were identified and validated by Western blotting and immunohistochemistry. These results demonstrate that proteomic analysis of endobronchial lesions may facilitate the diagnosis of lung cancer and the monitoring of high risk individuals for lung cancer in surveillance and chemoprevention trials. Early detection may help improve survival from lung cancer. In this study, our goal was to derive and validate a signature from the proteomic analysis of bronchial lesions that could predict the diagnosis of lung cancer. Using previously published studies of bronchial tissues, we selected a signature of nine matrix-assisted laser desorption ionization mass spectrometry (MALDI MS) mass-to-charge ratio features to build a prediction model diagnostic of lung cancer. The model was based on MALDI MS signal intensity (MALDI score) from bronchial tissue specimens from our 2005 published cohort of 51 patients. The performance of the prediction model in identifying lung cancer was tested in an independent cohort of bronchial specimens from 60 patients. The probability of having lung cancer based on the proteomic analysis of the bronchial specimens was characterized by an area under the receiver operating characteristic curve of 0.77 (95% CI 0.66–0.88) in this validation cohort. Eight of the nine features were identified and validated by Western blotting and immunohistochemistry. These results show that proteomic analysis of endobronchial lesions may facilitate the diagnosis of lung cancer and the monitoring of high-risk individuals for lung cancer in surveillance and chemoprevention trials. Cancer Res; 71(8); 3009–17. ©2011 AACR. |
Author | SHAH, Ronak N PUTNAM, Joe B ZHANG, Xueqiong J MILLER, York E MANIER, M. Lisa OLSON, Sandra J SHYR, Yu MASSION, Pierre P FRANKLIN, Wilbur A ZIMMERMAN, Lisa J SEELE, Erin H GONZALEZ, Adriana L JAMSHEDUR RAHMAN, S. M BLOT, William J MING LI CAPRIOLI, Richard M MILLER, Alison N CARBONE, David P |
Author_xml | – sequence: 1 givenname: S. M surname: JAMSHEDUR RAHMAN fullname: JAMSHEDUR RAHMAN, S. M organization: Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, United States – sequence: 2 givenname: Adriana L surname: GONZALEZ fullname: GONZALEZ, Adriana L organization: Department of Pathology, Vanderbilt University School of Medicine, United States – sequence: 3 givenname: Joe B surname: PUTNAM fullname: PUTNAM, Joe B organization: Department of Thoracic Surgery, Vanderbilt University School of Medicine, United States – sequence: 4 givenname: York E surname: MILLER fullname: MILLER, York E organization: Pulmonary Division, Department of Medicine, Denver Veterans Affairs Medical Center, United States – sequence: 5 givenname: Wilbur A surname: FRANKLIN fullname: FRANKLIN, Wilbur A organization: Department of Pathology, University of Colorado Denver, Denver, Colorado, United States – sequence: 6 givenname: William J surname: BLOT fullname: BLOT, William J organization: Epidemiology Division, Department of Medicine, Vanderbilt University School of Medicine, United States – sequence: 7 givenname: David P surname: CARBONE fullname: CARBONE, David P organization: Mass Spectrometry Research Center, Vanderbilt University School of Medicine, United States – sequence: 8 givenname: Yu surname: SHYR fullname: SHYR, Yu organization: Division of Cancer Biostatistics, Department of Biostatistics, Vanderbilt University School of Medicine, United States – sequence: 9 givenname: Richard M surname: CAPRIOLI fullname: CAPRIOLI, Richard M organization: Mass Spectrometry Research Center, Vanderbilt University School of Medicine, United States – sequence: 10 givenname: Pierre P surname: MASSION fullname: MASSION, Pierre P organization: Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, United States – sequence: 11 surname: MING LI fullname: MING LI organization: Division of Cancer Biostatistics, Department of Biostatistics, Vanderbilt University School of Medicine, United States – sequence: 12 givenname: Erin H surname: SEELE fullname: SEELE, Erin H organization: Mass Spectrometry Research Center, Vanderbilt University School of Medicine, United States – sequence: 13 givenname: Lisa J surname: ZIMMERMAN fullname: ZIMMERMAN, Lisa J organization: Department of Biochemistry, Vanderbilt University School of Medicine, United States – sequence: 14 givenname: Xueqiong J surname: ZHANG fullname: ZHANG, Xueqiong J organization: Division of Cancer Biostatistics, Department of Biostatistics, Vanderbilt University School of Medicine, United States – sequence: 15 givenname: M. Lisa surname: MANIER fullname: MANIER, M. Lisa organization: Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, United States – sequence: 16 givenname: Sandra J surname: OLSON fullname: OLSON, Sandra J organization: Department of Pathology, Vanderbilt University School of Medicine, United States – sequence: 17 givenname: Ronak N surname: SHAH fullname: SHAH, Ronak N organization: Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, United States – sequence: 18 givenname: Alison N surname: MILLER fullname: MILLER, Alison N organization: Division of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University School of Medicine, United States |
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Keywords | Lung disease Premalignant lesion Respiratory disease Analysis Lung cancer Proteomics Bronchus disease Malignant tumor Diagnosis Bronchopulmonary Cancer |
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Snippet | Early detection may help improve survival from lung cancer. In this study, our goal was to derive and validate a signature from the proteomic analysis of... Early detection may help improve survival from lung cancer. In this study our goal was to derive and validate a signature from the proteomic analysis of... |
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SubjectTerms | Aged Antineoplastic agents Biological and medical sciences Blotting, Western Early Detection of Cancer - methods Female Humans Immunohistochemistry Lung Neoplasms - diagnosis Lung Neoplasms - metabolism Male Medical sciences Middle Aged Neoplasm Proteins - analysis Neoplasm Proteins - metabolism Pharmacology. Drug treatments Pneumology Proteomics - methods Reproducibility of Results Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Tumors Tumors of the respiratory system and mediastinum |
Title | Lung Cancer Diagnosis from Proteomic Analysis of Preinvasive Lesions |
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