Id |
Subject |
Object |
Predicate |
Lexical cue |
TextSentencer_T1 |
0-104 |
Sentence |
denotes |
The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1. |
T1 |
0-104 |
Sentence |
denotes |
The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1. |
TextSentencer_T2 |
105-270 |
Sentence |
denotes |
Epithelial to mesenchymal transition (EMT) facilitates tissue remodelling during embryonic development and is viewed as an essential early step in tumour metastasis. |
T2 |
105-270 |
Sentence |
denotes |
Epithelial to mesenchymal transition (EMT) facilitates tissue remodelling during embryonic development and is viewed as an essential early step in tumour metastasis. |
TextSentencer_T3 |
271-571 |
Sentence |
denotes |
We found that all five members of the microRNA-200 family (miR-200a, miR-200b, miR-200c, miR-141 and miR-429) and miR-205 were markedly downregulated in cells that had undergone EMT in response to transforming growth factor (TGF)-beta or to ectopic expression of the protein tyrosine phosphatase Pez. |
T3 |
271-571 |
Sentence |
denotes |
We found that all five members of the microRNA-200 family (miR-200a, miR-200b, miR-200c, miR-141 and miR-429) and miR-205 were markedly downregulated in cells that had undergone EMT in response to transforming growth factor (TGF)-beta or to ectopic expression of the protein tyrosine phosphatase Pez. |
TextSentencer_T4 |
572-667 |
Sentence |
denotes |
Enforced expression of the miR-200 family alone was sufficient to prevent TGF-beta-induced EMT. |
T4 |
572-667 |
Sentence |
denotes |
Enforced expression of the miR-200 family alone was sufficient to prevent TGF-beta-induced EMT. |
TextSentencer_T5 |
668-893 |
Sentence |
denotes |
Together, these microRNAs cooperatively regulate expression of the E-cadherin transcriptional repressors ZEB1 (also known as deltaEF1) and SIP1 (also known as ZEB2), factors previously implicated in EMT and tumour metastasis. |
T5 |
668-893 |
Sentence |
denotes |
Together, these microRNAs cooperatively regulate expression of the E-cadherin transcriptional repressors ZEB1 (also known as deltaEF1) and SIP1 (also known as ZEB2), factors previously implicated in EMT and tumour metastasis. |
TextSentencer_T6 |
894-1007 |
Sentence |
denotes |
Inhibition of the microRNAs was sufficient to induce EMT in a process requiring upregulation of ZEB1 and/or SIP1. |
T6 |
894-1007 |
Sentence |
denotes |
Inhibition of the microRNAs was sufficient to induce EMT in a process requiring upregulation of ZEB1 and/or SIP1. |
TextSentencer_T7 |
1008-1132 |
Sentence |
denotes |
Conversely, ectopic expression of these microRNAs in mesenchymal cells initiated mesenchymal to epithelial transition (MET). |
T7 |
1008-1132 |
Sentence |
denotes |
Conversely, ectopic expression of these microRNAs in mesenchymal cells initiated mesenchymal to epithelial transition (MET). |
TextSentencer_T8 |
1133-1294 |
Sentence |
denotes |
Consistent with their role in regulating EMT, expression of these microRNAs was found to be lost in invasive breast cancer cell lines with mesenchymal phenotype. |
T8 |
1133-1294 |
Sentence |
denotes |
Consistent with their role in regulating EMT, expression of these microRNAs was found to be lost in invasive breast cancer cell lines with mesenchymal phenotype. |
TextSentencer_T9 |
1295-1411 |
Sentence |
denotes |
Expression of the miR-200 family was also lost in regions of metaplastic breast cancer specimens lacking E-cadherin. |
T9 |
1295-1411 |
Sentence |
denotes |
Expression of the miR-200 family was also lost in regions of metaplastic breast cancer specimens lacking E-cadherin. |
TextSentencer_T10 |
1412-1515 |
Sentence |
denotes |
These data suggest that downregulation of the microRNAs may be an important step in tumour progression. |
T10 |
1412-1515 |
Sentence |
denotes |
These data suggest that downregulation of the microRNAs may be an important step in tumour progression. |