| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-122 |
Sentence |
denotes |
Klotho, an anti-senescence related gene, is frequently inactivated through promoter hypermethylation in colorectal cancer. |
| T1 |
0-122 |
Sentence |
denotes |
Klotho, an anti-senescence related gene, is frequently inactivated through promoter hypermethylation in colorectal cancer. |
| TextSentencer_T2 |
123-307 |
Sentence |
denotes |
The potential anti-senescence gene Klotho (KL) has been recently found to participate in the progression of several different human cancers including breast, lung, and cervical cancer. |
| T2 |
123-307 |
Sentence |
denotes |
The potential anti-senescence gene Klotho (KL) has been recently found to participate in the progression of several different human cancers including breast, lung, and cervical cancer. |
| TextSentencer_T3 |
308-455 |
Sentence |
denotes |
In this current study, we identified KL as a candidate tumor suppressor gene silenced through promoter hypermethylation in colorectal cancer (CRC). |
| T3 |
308-455 |
Sentence |
denotes |
In this current study, we identified KL as a candidate tumor suppressor gene silenced through promoter hypermethylation in colorectal cancer (CRC). |
| TextSentencer_T4 |
456-677 |
Sentence |
denotes |
KL gene expression is found to be absent or reduced in colon cancer cell lines (5/6, 83.3%), which can be reversed by treatment with demethylation agent 5-aza-2'-deoxycytidine (Aza), but not HDAC inhibitor trichostatin A. |
| T4 |
456-677 |
Sentence |
denotes |
KL gene expression is found to be absent or reduced in colon cancer cell lines (5/6, 83.3%), which can be reversed by treatment with demethylation agent 5-aza-2'-deoxycytidine (Aza), but not HDAC inhibitor trichostatin A. |
| TextSentencer_T5 |
678-826 |
Sentence |
denotes |
In addition, KL expression is markedly downregulated in colorectal carcinoma tissues when compared to the adjacent nontumor tissues (n=25, p<0.001). |
| T5 |
678-826 |
Sentence |
denotes |
In addition, KL expression is markedly downregulated in colorectal carcinoma tissues when compared to the adjacent nontumor tissues (n=25, p<0.001). |
| TextSentencer_T6 |
827-980 |
Sentence |
denotes |
The methylation of the KL gene promoter was frequently detected in primary tumor tissues (34/40, 85%) when compared with adjacent nontumor colon tissues. |
| T6 |
827-980 |
Sentence |
denotes |
The methylation of the KL gene promoter was frequently detected in primary tumor tissues (34/40, 85%) when compared with adjacent nontumor colon tissues. |
| TextSentencer_T7 |
981-1153 |
Sentence |
denotes |
Furthermore, ectopic expression of KL led to the cell proliferation inhibition of colon cancer cell lines via the induction of cell apoptosis and S-phase cell cycle arrest. |
| T7 |
981-1153 |
Sentence |
denotes |
Furthermore, ectopic expression of KL led to the cell proliferation inhibition of colon cancer cell lines via the induction of cell apoptosis and S-phase cell cycle arrest. |
| TextSentencer_T8 |
1154-1307 |
Sentence |
denotes |
Taken together, our results suggest that KL is inactivated through promoter hypermethylation and potentially functions as a tumor suppressor gene in CRC. |
| T8 |
1154-1307 |
Sentence |
denotes |
Taken together, our results suggest that KL is inactivated through promoter hypermethylation and potentially functions as a tumor suppressor gene in CRC. |