| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-119 |
Sentence |
denotes |
Differentially expressed glycosylated patterns of α-1-antitrypsin as serum biomarkers for the diagnosis of lung cancer. |
| T1 |
0-119 |
Sentence |
denotes |
Differentially expressed glycosylated patterns of α-1-antitrypsin as serum biomarkers for the diagnosis of lung cancer. |
| T1 |
0-119 |
Sentence |
denotes |
Differentially expressed glycosylated patterns of α-1-antitrypsin as serum biomarkers for the diagnosis of lung cancer. |
| TextSentencer_T2 |
120-172 |
Sentence |
denotes |
Lung cancer is the most common malignancy worldwide. |
| T2 |
120-172 |
Sentence |
denotes |
Lung cancer is the most common malignancy worldwide. |
| T2 |
120-172 |
Sentence |
denotes |
Lung cancer is the most common malignancy worldwide. |
| TextSentencer_T3 |
173-298 |
Sentence |
denotes |
Thus, there is a critical need for diagnostic biomarkers with adequate sensitivity and specificity for lung cancer detection. |
| T3 |
173-298 |
Sentence |
denotes |
Thus, there is a critical need for diagnostic biomarkers with adequate sensitivity and specificity for lung cancer detection. |
| T3 |
173-298 |
Sentence |
denotes |
Thus, there is a critical need for diagnostic biomarkers with adequate sensitivity and specificity for lung cancer detection. |
| TextSentencer_T4 |
299-433 |
Sentence |
denotes |
Glycans in glycoproteins are significantly altered in cancer, and may serve as a tool for identifying potential diagnostic biomarkers. |
| T4 |
299-433 |
Sentence |
denotes |
Glycans in glycoproteins are significantly altered in cancer, and may serve as a tool for identifying potential diagnostic biomarkers. |
| T4 |
299-433 |
Sentence |
denotes |
Glycans in glycoproteins are significantly altered in cancer, and may serve as a tool for identifying potential diagnostic biomarkers. |
| TextSentencer_T5 |
434-555 |
Sentence |
denotes |
Recent studies have reported changes in α-1-antitrypsin (A1AT) glycosylation in lung cancer serum, tissue and cell lines. |
| T5 |
434-555 |
Sentence |
denotes |
Recent studies have reported changes in α-1-antitrypsin (A1AT) glycosylation in lung cancer serum, tissue and cell lines. |
| T5 |
434-555 |
Sentence |
denotes |
Recent studies have reported changes in α-1-antitrypsin (A1AT) glycosylation in lung cancer serum, tissue and cell lines. |
| TextSentencer_T6 |
556-779 |
Sentence |
denotes |
In this study, a lectin microarray was used to detect glycosylation changes in serum A1AT from patients with lung adenocarcinoma (ADC), squamous cell lung cancer, small-cell lung cancer (SCLC) and benign pulmonary diseases. |
| T6 |
556-779 |
Sentence |
denotes |
In this study, a lectin microarray was used to detect glycosylation changes in serum A1AT from patients with lung adenocarcinoma (ADC), squamous cell lung cancer, small-cell lung cancer (SCLC) and benign pulmonary diseases. |
| T6 |
556-779 |
Sentence |
denotes |
In this study, a lectin microarray was used to detect glycosylation changes in serum A1AT from patients with lung adenocarcinoma (ADC), squamous cell lung cancer, small-cell lung cancer (SCLC) and benign pulmonary diseases. |
| TextSentencer_T7 |
780-945 |
Sentence |
denotes |
Differentially expressed glycosylated patterns of A1AT were identified by lectin arrays and were confirmed by lectin-based enzyme-linked immunosorbent assay (ELISA). |
| T7 |
780-945 |
Sentence |
denotes |
Differentially expressed glycosylated patterns of A1AT were identified by lectin arrays and were confirmed by lectin-based enzyme-linked immunosorbent assay (ELISA). |
| T7 |
780-945 |
Sentence |
denotes |
Differentially expressed glycosylated patterns of A1AT were identified by lectin arrays and were confirmed by lectin-based enzyme-linked immunosorbent assay (ELISA). |
| TextSentencer_T8 |
946-1336 |
Sentence |
denotes |
We found that galactosylated A1AT could distinguish non-small-cell lung cancer (NSCLC) from benign pulmonary diseases (AUC = 0.834); fucosylated A1AT showed exceptional capability in distinguishing ADC from benign diseases (AUC = 0.919) or other lung cancer subtypes (AUC = 0.844), and A1AT containing poly-LacNAc could detect SCLC from benign diseases (AUC = 0.905) or NSCLC (AUC = 0.707). |
| T8 |
946-1336 |
Sentence |
denotes |
We found that galactosylated A1AT could distinguish non-small-cell lung cancer (NSCLC) from benign pulmonary diseases (AUC = 0.834); fucosylated A1AT showed exceptional capability in distinguishing ADC from benign diseases (AUC = 0.919) or other lung cancer subtypes (AUC = 0.844), and A1AT containing poly-LacNAc could detect SCLC from benign diseases (AUC = 0.905) or NSCLC (AUC = 0.707). |
| T8 |
946-1336 |
Sentence |
denotes |
We found that galactosylated A1AT could distinguish non-small-cell lung cancer (NSCLC) from benign pulmonary diseases (AUC = 0.834); fucosylated A1AT showed exceptional capability in distinguishing ADC from benign diseases (AUC = 0.919) or other lung cancer subtypes (AUC = 0.844), and A1AT containing poly-LacNAc could detect SCLC from benign diseases (AUC = 0.905) or NSCLC (AUC = 0.707). |
| TextSentencer_T9 |
1337-1463 |
Sentence |
denotes |
The present study indicates that glycosylated patterns of A1AT may serve as potential biomarkers for detection of lung cancer. |
| T9 |
1337-1463 |
Sentence |
denotes |
The present study indicates that glycosylated patterns of A1AT may serve as potential biomarkers for detection of lung cancer. |
| T9 |
1337-1463 |
Sentence |
denotes |
The present study indicates that glycosylated patterns of A1AT may serve as potential biomarkers for detection of lung cancer. |
| TextSentencer_T10 |
1464-1567 |
Sentence |
denotes |
Further studies in larger sample sizes are necessary to validate the clinical utility of these markers. |
| T10 |
1464-1567 |
Sentence |
denotes |
Further studies in larger sample sizes are necessary to validate the clinical utility of these markers. |
| T10 |
1464-1567 |
Sentence |
denotes |
Further studies in larger sample sizes are necessary to validate the clinical utility of these markers. |