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Blood-based lung cancer biomarkers identified through proteomic discovery in cancer tissues,cell lines and conditioned medium
Authors:Charles E. Birse  Robert J. Lagier  William FitzHugh  Harvey I. Pass  William N. Rom  Eric S. Edell  Aaron O. Bungum  Fabien Maldonado  James R. Jett  Mehdi Mesri  Erin Sult  Elizabeth Joseloff  Aiqun Li  Jenny Heidbrink  Gulshan Dhariwal  Chad Danis  Jennifer L. Tomic  Robert J. Bruce  Paul A. Moore  Tao He  Marcia E. Lewis  Steve M. Ruben
Affiliation:.Celera employees during the course of these studies, Celera, 1311 Harbor Bay Parkway, Alameda, CA 94502 USA ;.Department of Cardiothoracic Surgery, NYU Langone Medical Center, 530 First Avenue, New York, NY USA ;.Division of Pulmonary, Critical Care, and Sleep Medicine, NYU School of Medicine, New York, NY USA ;.Division of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN USA ;.Division of Oncology, National Jewish Health, Denver, CO USA
Abstract:

Background

Support for early detection of lung cancer has emerged from the National Lung Screening Trial (NLST), in which low-dose computed tomography (LDCT) screening reduced lung cancer mortality by 20 % relative to chest x-ray. The US Preventive Services Task Force (USPSTF) recently recommended annual screening for the high-risk population, concluding that the benefits (life years gained) outweighed harms (false positive findings, abortive biopsy/surgery, radiation exposure). In making their recommendation, the USPSTF noted that the moderate net benefit of screening was dependent on the resolution of most false-positive results without invasive procedures. Circulating biomarkers may serve as a valuable adjunctive tool to imaging.

Results

We developed a broad-based proteomics discovery program, integrating liquid chromatography/mass spectrometry (LC/MS) analyses of freshly resected lung tumor specimens (n = 13), lung cancer cell lines (n = 17), and conditioned media collected from tumor cell lines (n = 7). To enrich for biomarkers likely to be found at elevated levels in the peripheral circulation of lung cancer patients, proteins were prioritized based on predicted subcellular localization (secreted, cell-membrane associated) and differential expression in disease samples. 179 candidate biomarkers were identified. Several markers selected for further validation showed elevated levels in serum collected from subjects with stage I NSCLC (n = 94), relative to healthy smoker controls (n = 189). An 8-marker model was developed (TFPI, MDK, OPN, MMP2, TIMP1, CEA, CYFRA 21–1, SCC) which accurately distinguished subjects with lung cancer (n = 50) from high risk smokers (n = 50) in an independent validation study (AUC = 0.775).

Conclusions

Integrating biomarker discovery from multiple sample types (fresh tissue, cell lines and conditioned medium) has resulted in a diverse repertoire of candidate biomarkers. This unique collection of biomarkers may have clinical utility in lung cancer detection and diagnoses.

Electronic supplementary material

The online version of this article (doi:10.1186/s12014-015-9090-9) contains supplementary material, which is available to authorized users.
Keywords:Lung cancer   Early detection   Biomarker   Mass spectrometry   Proteomics   Discovery
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