| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-78 |
Sentence |
denotes |
p53-Independent regulation of p21Waf1/Cip1 expression and senescence by PRMT6. |
| T1 |
0-78 |
Sentence |
denotes |
p53-Independent regulation of p21Waf1/Cip1 expression and senescence by PRMT6. |
| TextSentencer_T2 |
79-205 |
Sentence |
denotes |
p21 is a potent cyclin-dependent kinase inhibitor that plays a role in promoting G1 cell cycle arrest and cellular senescence. |
| T2 |
79-205 |
Sentence |
denotes |
p21 is a potent cyclin-dependent kinase inhibitor that plays a role in promoting G1 cell cycle arrest and cellular senescence. |
| TextSentencer_T3 |
206-381 |
Sentence |
denotes |
Consistent with this role, p21 is a downstream target of several tumour suppressors and oncogenes, and it is downregulated in the majority of tumours, including breast cancer. |
| T3 |
206-381 |
Sentence |
denotes |
Consistent with this role, p21 is a downstream target of several tumour suppressors and oncogenes, and it is downregulated in the majority of tumours, including breast cancer. |
| TextSentencer_T4 |
382-543 |
Sentence |
denotes |
Here, we report that protein arginine methyltransferase 6 (PRMT6), a type I PRMT known to act as a transcriptional cofactor, directly represses the p21 promoter. |
| T4 |
382-543 |
Sentence |
denotes |
Here, we report that protein arginine methyltransferase 6 (PRMT6), a type I PRMT known to act as a transcriptional cofactor, directly represses the p21 promoter. |
| TextSentencer_T5 |
544-823 |
Sentence |
denotes |
PRMT6 knock-down (KD) results in a p21 derepression in breast cancer cells, which is p53-independent, and leads to cell cycle arrest, cellular senescence and reduced growth in soft agar assays and in severe combined immunodeficiency (SCID) mice for all the cancer lines examined. |
| T5 |
544-823 |
Sentence |
denotes |
PRMT6 knock-down (KD) results in a p21 derepression in breast cancer cells, which is p53-independent, and leads to cell cycle arrest, cellular senescence and reduced growth in soft agar assays and in severe combined immunodeficiency (SCID) mice for all the cancer lines examined. |
| TextSentencer_T6 |
824-970 |
Sentence |
denotes |
We finally show that bypassing the p21-mediated arrest rescues PRMT6 KD cells from senescence, and it restores their ability to grow on soft agar. |
| T6 |
824-970 |
Sentence |
denotes |
We finally show that bypassing the p21-mediated arrest rescues PRMT6 KD cells from senescence, and it restores their ability to grow on soft agar. |
| TextSentencer_T7 |
971-1132 |
Sentence |
denotes |
We conclude that PRMT6 acts as an oncogene in breast cancer cells, promoting growth and preventing senescence, making it an attractive target for cancer therapy. |
| T7 |
971-1132 |
Sentence |
denotes |
We conclude that PRMT6 acts as an oncogene in breast cancer cells, promoting growth and preventing senescence, making it an attractive target for cancer therapy. |