| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-82 |
Sentence |
denotes |
Tumor-suppressive functions of long-chain acyl-CoA synthetase 4 in gastric cancer. |
| T1 |
0-82 |
Sentence |
denotes |
Tumor-suppressive functions of long-chain acyl-CoA synthetase 4 in gastric cancer. |
| TextSentencer_T2 |
83-214 |
Sentence |
denotes |
Long chain acyl CoA synthetase 4 (ACSL4) is a key enzyme in fatty acid metabolism with marked preference for arachidonic acid (AA). |
| T2 |
83-214 |
Sentence |
denotes |
Long chain acyl CoA synthetase 4 (ACSL4) is a key enzyme in fatty acid metabolism with marked preference for arachidonic acid (AA). |
| TextSentencer_T3 |
215-281 |
Sentence |
denotes |
Recent reports have implicated its crucial roles in tumorigenesis. |
| T3 |
215-281 |
Sentence |
denotes |
Recent reports have implicated its crucial roles in tumorigenesis. |
| TextSentencer_T4 |
282-366 |
Sentence |
denotes |
However in gastric cancer (GC), the expression and function of ACSL4 remain unclear. |
| T4 |
282-366 |
Sentence |
denotes |
However in gastric cancer (GC), the expression and function of ACSL4 remain unclear. |
| TextSentencer_T5 |
367-447 |
Sentence |
denotes |
In the present study, we identified ACSL4 as a potential tumor suppressor in GC. |
| T5 |
367-447 |
Sentence |
denotes |
In the present study, we identified ACSL4 as a potential tumor suppressor in GC. |
| TextSentencer_T6 |
448-539 |
Sentence |
denotes |
The ACSL4 expression in GC samples was evaluated by real-time PCR and immunohistochemistry. |
| T6 |
448-539 |
Sentence |
denotes |
The ACSL4 expression in GC samples was evaluated by real-time PCR and immunohistochemistry. |
| TextSentencer_T7 |
540-716 |
Sentence |
denotes |
The results indicated that the mRNA and protein levels of ACSL4 were frequently downregulated in cancer tissues compared with the adjacent non-cancerous mucosa control tissues. |
| T7 |
540-716 |
Sentence |
denotes |
The results indicated that the mRNA and protein levels of ACSL4 were frequently downregulated in cancer tissues compared with the adjacent non-cancerous mucosa control tissues. |
| TextSentencer_T8 |
717-895 |
Sentence |
denotes |
Cell-based functional assays exhibited that ectopic expression of ACSL4 inhibits cell growth, colony formation and cell migration, whereas ACSL4 knockdown enhanced these effects. |
| T8 |
717-895 |
Sentence |
denotes |
Cell-based functional assays exhibited that ectopic expression of ACSL4 inhibits cell growth, colony formation and cell migration, whereas ACSL4 knockdown enhanced these effects. |
| TextSentencer_T9 |
896-988 |
Sentence |
denotes |
In a nude mice model, ACSL4 knockdown also promoted subcutaneous xenografts' growth in vivo. |
| T9 |
896-988 |
Sentence |
denotes |
In a nude mice model, ACSL4 knockdown also promoted subcutaneous xenografts' growth in vivo. |
| TextSentencer_T10 |
989-1106 |
Sentence |
denotes |
Moreover, western blot analysis revealed that ACSL4 expression had a significant effect on FAK and P21 protein level. |
| T10 |
989-1106 |
Sentence |
denotes |
Moreover, western blot analysis revealed that ACSL4 expression had a significant effect on FAK and P21 protein level. |
| TextSentencer_T11 |
1107-1222 |
Sentence |
denotes |
These findings suggest that ACSL4 plays a tumor-suppressive role and could be a potential therapeutic target in GC. |
| T11 |
1107-1222 |
Sentence |
denotes |
These findings suggest that ACSL4 plays a tumor-suppressive role and could be a potential therapeutic target in GC. |