Surfactant protein B gene variations and susceptibility to lung cancer in chromate workers

2006 ◽  
Vol 49 (5) ◽  
pp. 367-373 ◽  
Author(s):  
Ashraf A. Ewis ◽  
Kazuya Kondo ◽  
Fuquan Dang ◽  
Yutaka Nakahori ◽  
Yasuo Shinohara ◽  
...  
2013 ◽  
Vol 22 (10) ◽  
pp. 1756-1761 ◽  
Author(s):  
Ayumu Taguchi ◽  
Samir Hanash ◽  
Andrew Rundle ◽  
Ian W. McKeague ◽  
Deliang Tang ◽  
...  

Lung Cancer ◽  
2000 ◽  
Vol 29 (1) ◽  
pp. 226
Author(s):  
C Seifart ◽  
U Seifart ◽  
A Neubauer ◽  
M Wolf ◽  
P von Wichert

2015 ◽  
Vol 45 (4) ◽  
pp. 1037-1045 ◽  
Author(s):  
Janice M. Leung ◽  
John Mayo ◽  
Wan Tan ◽  
C. Martin Tammemagi ◽  
Geoffrey Liu ◽  
...  

Plasma pro-surfactant protein B (pro-SFTPB) levels have recently been shown to predict the development of lung cancer in current and ex-smokers, but the ability of pro-SFTPB to predict measures of chronic obstructive pulmonary disease (COPD) severity is unknown. We evaluated the performance characteristics of pro-SFTPB as a biomarker of lung function decline in a population of current and ex-smokers.Plasma pro-SFTPB levels were measured in 2503 current and ex-smokers enrolled in the Pan-Canadian Early Detection of Lung Cancer Study. Linear regression was performed to determine the relationship of pro-SFTPB levels to changes in forced expiratory volume in 1 s (FEV1) over a 2-year period as well as to baseline FEV1 and the burden of emphysema observed in computed tomography (CT) scans.Plasma pro-SFTPB levels were inversely related to both FEV1 % predicted (p=0.024) and FEV1/forced vital capacity (FVC) (p<0.001), and were positively related to the burden of emphysema on CT scans (p<0.001). Higher plasma pro-SFTPB levels were also associated with a more rapid decline in FEV1 at 1 year (p=0.024) and over 2 years of follow-up (p=0.004).Higher plasma pro-SFTPB levels are associated with increased severity of airflow limitation and accelerated decline in lung function. Pro-SFTPB is a promising biomarker for COPD severity and progression.


2014 ◽  
Vol 20 (2 Supplement) ◽  
pp. PR08-PR08
Author(s):  
Don D. Sin ◽  
C Martin Tammemagi ◽  
Stephen Lam ◽  
Matt J. Barnett ◽  
Xiaobo Duan ◽  
...  

2013 ◽  
Vol 31 (36) ◽  
pp. 4536-4543 ◽  
Author(s):  
Don D. Sin ◽  
C. Martin Tammemagi ◽  
Stephen Lam ◽  
Matt J. Barnett ◽  
Xiaobo Duan ◽  
...  

Purpose Preliminary studies have identified pro–surfactant protein B (pro-SFTPB) to be a promising blood biomarker for non–small-cell lung cancer. We conducted a study to determine the independent predictive potential of pro-SFTPB in identifying individuals who are subsequently diagnosed with lung cancer. Patients and Methods Pro-SFTPB levels were measured in 2,485 individuals, who enrolled onto the Pan-Canadian Early Detection of Lung Cancer Study by using plasma sample collected at the baseline visit. Multivariable logistic regression models were used to evaluate the predictive ability of pro-SFTPB in addition to known lung cancer risk factors. Calibration and discrimination were evaluated, the latter by an area under the receiver operating characteristic curve (AUC). External validation was performed with samples collected in the Carotene and Retinol Efficacy Trial (CARET) participants using a case-control study design. Results Adjusted for age, sex, body mass index, personal history of cancer, family history of lung cancer, forced expiratory volume in one second percent predicted, average number of cigarettes smoked per day, and smoking duration, pro-SFTPB (log transformed) had an odds ratio of 2.220 (95% CI, 1.727 to 2.853; P < .001). The AUCs of the full model with and without pro-SFTPB were 0.741 (95% CI, 0.696 to 0.783) and 0.669 (95% CI, 0.620 to 0.717; difference in AUC P < .001). In the CARET Study, the use of pro-SFPTB yielded an AUC of 0.683 (95% CI, 0.604 to 0.761). Conclusion Pro-SFTPB in plasma is an independent predictor of lung cancer and may be a valuable addition to existing lung cancer risk prediction models.


2015 ◽  
Vol 33 (33) ◽  
pp. 3880-3886 ◽  
Author(s):  
William R. Wikoff ◽  
Samir Hanash ◽  
Brian DeFelice ◽  
Suzanne Miyamoto ◽  
Matt Barnett ◽  
...  

Purpose We have investigated the potential of metabolomics to discover blood-based biomarkers relevant to lung cancer screening and early detection. An untargeted metabolomics approach was applied to identify biomarker candidates using prediagnostic sera from the Beta-Carotene and Retinol Efficacy Trial (CARET) study. Patients and Methods A liquid chromatography/mass spectrometry hydrophilic interaction method designed to profile a wide range of metabolites was applied to prediagnostic serum samples from CARET participants (current or former heavy smokers), consisting of 100 patients who subsequently developed non–small-cell lung cancer (NSCLC) and 199 matched controls. A separate aliquot was used to quantify levels of pro-surfactant protein B (pro-SFTPB), a previously established protein biomarker for NSCLC. On the basis of the results from the discovery set, blinded validation of a metabolite, identified as N1,N12-diacetylspermine (DAS), and pro-SFTPB was performed using an independent set of CARET prediagnostic sera from 108 patients with NSCLC and 216 matched controls. Results Serum DAS was elevated by 1.9-fold, demonstrating significant specificity and sensitivity in the discovery set for samples collected up to 6 months before diagnosis of NSCLC. In addition, DAS significantly complemented performance of pro-SFTPB in both the discovery and validations sets, with a combined area under the curve in the validation set of 0.808 (P < .001 v pro-SFTPB). Conclusion DAS is a novel serum metabolite with significant performance in prediagnostic NSCLC and has additive performance with pro-SFTPB.


2017 ◽  
pp. 66-71
Author(s):  
O. Yablon ◽  
◽  
N. Zaichko ◽  
O. Mazulov ◽  
Z.I. Rossokha ◽  
...  

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