AI Article Synopsis

  • The National Lung Screening Trial demonstrated that low-dose computed tomography (LDCT) can significantly reduce lung cancer mortality, leading to recommendations for annual screening in high-risk populations by the US Preventive Services Task Force.
  • A research program identified 179 potential circulating biomarkers associated with lung cancer by analyzing lung tumor samples and cell lines, focusing on proteins that could be found in patients’ blood.
  • An 8-marker model was created to effectively differentiate between lung cancer patients and high-risk smokers, suggesting that these biomarkers could enhance the accuracy of early lung cancer detection alongside imaging techniques.

Article 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537594PMC
http://dx.doi.org/10.1186/s12014-015-9090-9DOI Listing

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