| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-95 |
Sentence |
denotes |
OSMR gene effect on the pathogenesis of chronic autoimmune Urticaria via the JAK/STAT3 pathway. |
| T1 |
0-95 |
Sentence |
denotes |
OSMR gene effect on the pathogenesis of chronic autoimmune Urticaria via the JAK/STAT3 pathway. |
| T2 |
96-107 |
Sentence |
denotes |
BACKGROUND: |
| T2 |
96-107 |
Sentence |
denotes |
BACKGROUND: |
| T3 |
108-248 |
Sentence |
denotes |
Chronic autoimmune urticaria (CAU) is a common skin disease and remains unclear understanding of pathogenesis in the vast majority of cases. |
| T3 |
108-248 |
Sentence |
denotes |
Chronic autoimmune urticaria (CAU) is a common skin disease and remains unclear understanding of pathogenesis in the vast majority of cases. |
| T4 |
249-482 |
Sentence |
denotes |
In order to explore a new therapy for CAU, the current study was performed to investigate the possible functioning of the Oncostatin M receptor (OSMR) gene in the autoimmunity of CAU via regulation of the JAK/STAT3 signaling pathway. |
| T4 |
249-482 |
Sentence |
denotes |
In order to explore a new therapy for CAU, the current study was performed to investigate the possible functioning of the Oncostatin M receptor (OSMR) gene in the autoimmunity of CAU via regulation of the JAK/STAT3 signaling pathway. |
| T5 |
483-590 |
Sentence |
denotes |
METHODS: CAU skin tissues from 24 CAU patients and normal skin tissues from normal subjects were collected. |
| T5 |
483-590 |
Sentence |
denotes |
METHODS: CAU skin tissues from 24 CAU patients and normal skin tissues from normal subjects were collected. |
| T6 |
591-776 |
Sentence |
denotes |
Hematoxylin-eosin (HE) staining was conducted to count eosinophils, and immunohistochemistry was carried out to detect the positive rate of OSMR expression in two kinds of skin tissues. |
| T6 |
591-776 |
Sentence |
denotes |
Hematoxylin-eosin (HE) staining was conducted to count eosinophils, and immunohistochemistry was carried out to detect the positive rate of OSMR expression in two kinds of skin tissues. |
| T7 |
777-920 |
Sentence |
denotes |
A total of 72 Kunming (KM) mice were selected, and 60 mice were used for establishing CAU models and later transfected with different plasmids. |
| T7 |
777-920 |
Sentence |
denotes |
A total of 72 Kunming (KM) mice were selected, and 60 mice were used for establishing CAU models and later transfected with different plasmids. |
| T8 |
921-1020 |
Sentence |
denotes |
The expression of inflammatory factors was evaluated by enzyme-linked immunosorbent assays (ELISA). |
| T8 |
921-1020 |
Sentence |
denotes |
The expression of inflammatory factors was evaluated by enzyme-linked immunosorbent assays (ELISA). |
| T9 |
1021-1342 |
Sentence |
denotes |
Expressions of janus kinase (JAK), signal transducer and activator of transcription 3 (STAT3), interferon-stimulated gene 15 (ISG15), CT10-regulated kinase (CRK), and interferon regulatory factor 9 (IRF9) were identified using Western blot assay and reverse transcription quantitative polymerase chain reaction (RT-qPCR). |
| T9 |
1021-1342 |
Sentence |
denotes |
Expressions of janus kinase (JAK), signal transducer and activator of transcription 3 (STAT3), interferon-stimulated gene 15 (ISG15), CT10-regulated kinase (CRK), and interferon regulatory factor 9 (IRF9) were identified using Western blot assay and reverse transcription quantitative polymerase chain reaction (RT-qPCR). |
| T10 |
1343-1546 |
Sentence |
denotes |
Epithelial cell proliferation was assessed by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MTT) assay, and cell cycle distribution and cell apoptosis were assessed using flow cytometry. |
| T10 |
1343-1546 |
Sentence |
denotes |
Epithelial cell proliferation was assessed by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide (MTT) assay, and cell cycle distribution and cell apoptosis were assessed using flow cytometry. |
| T11 |
1547-1555 |
Sentence |
denotes |
RESULTS: |
| T11 |
1547-1555 |
Sentence |
denotes |
RESULTS: |
| T12 |
1556-1806 |
Sentence |
denotes |
The findings confirm that OSMR protein expression and histamine release rate are highly elevated in human CAU skin tissues, and the expression of the JAK/STAT3 signaling pathway-related genes (OSMR, JAK2, STAT3, ISG15, CRK and IRF9) was up-regulated. |
| T12 |
1556-1806 |
Sentence |
denotes |
The findings confirm that OSMR protein expression and histamine release rate are highly elevated in human CAU skin tissues, and the expression of the JAK/STAT3 signaling pathway-related genes (OSMR, JAK2, STAT3, ISG15, CRK and IRF9) was up-regulated. |
| T13 |
1807-2143 |
Sentence |
denotes |
OSMR gene silencing in CAU mice significantly decreases the content of inflammatory factors (IL-1, IL-6, IFN-γ, and IgE), the number of eosinophils, and reduces the expression of the JAK/STAT3 signaling pathway related genes, and further enhances cell proliferation, promotes cell cycle entry and inhibits apoptosis of epithelial cells. |
| T13 |
1807-2143 |
Sentence |
denotes |
OSMR gene silencing in CAU mice significantly decreases the content of inflammatory factors (IL-1, IL-6, IFN-γ, and IgE), the number of eosinophils, and reduces the expression of the JAK/STAT3 signaling pathway related genes, and further enhances cell proliferation, promotes cell cycle entry and inhibits apoptosis of epithelial cells. |
| T14 |
2144-2155 |
Sentence |
denotes |
CONCLUSION: |
| T14 |
2144-2155 |
Sentence |
denotes |
CONCLUSION: |
| T15 |
2156-2320 |
Sentence |
denotes |
All aforementioned results indicate that OSMR gene silencing inhibits the activation of the JAK/STAT3 signaling pathway, thereby suppressing the development of CAU. |
| T15 |
2156-2320 |
Sentence |
denotes |
All aforementioned results indicate that OSMR gene silencing inhibits the activation of the JAK/STAT3 signaling pathway, thereby suppressing the development of CAU. |