| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-134 |
Sentence |
denotes |
Expression of stage-specific embryonic antigen-4 (SSEA-4) defines spontaneous loss of epithelial phenotype in human solid tumor cells. |
| T1 |
0-134 |
Sentence |
denotes |
Expression of stage-specific embryonic antigen-4 (SSEA-4) defines spontaneous loss of epithelial phenotype in human solid tumor cells. |
| T1 |
0-134 |
Sentence |
denotes |
Expression of stage-specific embryonic antigen-4 (SSEA-4) defines spontaneous loss of epithelial phenotype in human solid tumor cells. |
| TextSentencer_T2 |
135-285 |
Sentence |
denotes |
Stage-specific embryonic antigen-4 (SSEA-4) is a glycosphingolipid, which is overexpressed in some cancers and has been linked to disease progression. |
| T2 |
135-285 |
Sentence |
denotes |
Stage-specific embryonic antigen-4 (SSEA-4) is a glycosphingolipid, which is overexpressed in some cancers and has been linked to disease progression. |
| T2 |
135-285 |
Sentence |
denotes |
Stage-specific embryonic antigen-4 (SSEA-4) is a glycosphingolipid, which is overexpressed in some cancers and has been linked to disease progression. |
| TextSentencer_T3 |
286-398 |
Sentence |
denotes |
However, little is known about the functions of SSEA-4 and the characteristics of SSEA-4 expressing tumor cells. |
| T3 |
286-398 |
Sentence |
denotes |
However, little is known about the functions of SSEA-4 and the characteristics of SSEA-4 expressing tumor cells. |
| T3 |
286-398 |
Sentence |
denotes |
However, little is known about the functions of SSEA-4 and the characteristics of SSEA-4 expressing tumor cells. |
| TextSentencer_T4 |
399-530 |
Sentence |
denotes |
Our studies identified SSEA-4 expression on a subpopulation of cells in many solid tumor cell lines but not in leukemic cell lines. |
| T4 |
399-530 |
Sentence |
denotes |
Our studies identified SSEA-4 expression on a subpopulation of cells in many solid tumor cell lines but not in leukemic cell lines. |
| T4 |
399-530 |
Sentence |
denotes |
Our studies identified SSEA-4 expression on a subpopulation of cells in many solid tumor cell lines but not in leukemic cell lines. |
| TextSentencer_T5 |
531-739 |
Sentence |
denotes |
Fluorescence-activated cell sorting-sorted SSEA-4(+) prostate cancer cells formed fibroblast-like colonies with limited cell-cell contacts, whereas SSEA-4(-) cells formed cobblestone-like epithelial colonies. |
| T5 |
531-739 |
Sentence |
denotes |
Fluorescence-activated cell sorting-sorted SSEA-4(+) prostate cancer cells formed fibroblast-like colonies with limited cell-cell contacts, whereas SSEA-4(-) cells formed cobblestone-like epithelial colonies. |
| T5 |
531-739 |
Sentence |
denotes |
Fluorescence-activated cell sorting-sorted SSEA-4(+) prostate cancer cells formed fibroblast-like colonies with limited cell-cell contacts, whereas SSEA-4(-) cells formed cobblestone-like epithelial colonies. |
| TextSentencer_T6 |
740-841 |
Sentence |
denotes |
Only colonies derived from SSEA-4(+) cells were enriched for pluripotent embryonic stem cell markers. |
| T6 |
740-841 |
Sentence |
denotes |
Only colonies derived from SSEA-4(+) cells were enriched for pluripotent embryonic stem cell markers. |
| T6 |
740-841 |
Sentence |
denotes |
Only colonies derived from SSEA-4(+) cells were enriched for pluripotent embryonic stem cell markers. |
| TextSentencer_T7 |
842-1005 |
Sentence |
denotes |
Moreover, major epithelial cell-associated markers Claudin-7, E-cadherin, ESRP1 and GRHL2 were down-regulated in the SSEA-4(+) fraction of DU145 and HCT-116 cells. |
| T7 |
842-1005 |
Sentence |
denotes |
Moreover, major epithelial cell-associated markers Claudin-7, E-cadherin, ESRP1 and GRHL2 were down-regulated in the SSEA-4(+) fraction of DU145 and HCT-116 cells. |
| T7 |
842-1005 |
Sentence |
denotes |
Moreover, major epithelial cell-associated markers Claudin-7, E-cadherin, ESRP1 and GRHL2 were down-regulated in the SSEA-4(+) fraction of DU145 and HCT-116 cells. |
| TextSentencer_T8 |
1006-1134 |
Sentence |
denotes |
Similar to cell lines, SSEA-4(+) primary prostate tumor cells also showed down-regulation of epithelial cell-associated markers. |
| T8 |
1006-1134 |
Sentence |
denotes |
Similar to cell lines, SSEA-4(+) primary prostate tumor cells also showed down-regulation of epithelial cell-associated markers. |
| T8 |
1006-1134 |
Sentence |
denotes |
Similar to cell lines, SSEA-4(+) primary prostate tumor cells also showed down-regulation of epithelial cell-associated markers. |
| TextSentencer_T9 |
1135-1245 |
Sentence |
denotes |
In addition, they showed up-regulation of epithelial-to-mesenchymal transition as well as mesenchymal markers. |
| T9 |
1135-1245 |
Sentence |
denotes |
In addition, they showed up-regulation of epithelial-to-mesenchymal transition as well as mesenchymal markers. |
| T9 |
1135-1245 |
Sentence |
denotes |
In addition, they showed up-regulation of epithelial-to-mesenchymal transition as well as mesenchymal markers. |
| TextSentencer_T10 |
1246-1462 |
Sentence |
denotes |
Furthermore, SSEA-4(+) cells escape from adhesive colonies spontaneously and form invadopodia-like migratory structures, in which SSEA-4, cortactin as well as active pPI3K, pAkt and pSrc are enriched and colocalized. |
| T10 |
1246-1462 |
Sentence |
denotes |
Furthermore, SSEA-4(+) cells escape from adhesive colonies spontaneously and form invadopodia-like migratory structures, in which SSEA-4, cortactin as well as active pPI3K, pAkt and pSrc are enriched and colocalized. |
| T10 |
1246-1462 |
Sentence |
denotes |
Furthermore, SSEA-4(+) cells escape from adhesive colonies spontaneously and form invadopodia-like migratory structures, in which SSEA-4, cortactin as well as active pPI3K, pAkt and pSrc are enriched and colocalized. |
| TextSentencer_T11 |
1463-1642 |
Sentence |
denotes |
Finally, SSEA-4(+) cells displayed strong tumorigenic ability and stable knockdown of SSEA-4 synthesis resulted in decreased cellular adhesion to different extracellular matrices. |
| T11 |
1463-1642 |
Sentence |
denotes |
Finally, SSEA-4(+) cells displayed strong tumorigenic ability and stable knockdown of SSEA-4 synthesis resulted in decreased cellular adhesion to different extracellular matrices. |
| T11 |
1463-1642 |
Sentence |
denotes |
Finally, SSEA-4(+) cells displayed strong tumorigenic ability and stable knockdown of SSEA-4 synthesis resulted in decreased cellular adhesion to different extracellular matrices. |
| TextSentencer_T12 |
1643-1762 |
Sentence |
denotes |
In conclusion, we introduce SSEA-4 as a novel marker to identify heterogeneous, invasive subpopulations of tumor cells. |
| T12 |
1643-1762 |
Sentence |
denotes |
In conclusion, we introduce SSEA-4 as a novel marker to identify heterogeneous, invasive subpopulations of tumor cells. |
| T12 |
1643-1762 |
Sentence |
denotes |
In conclusion, we introduce SSEA-4 as a novel marker to identify heterogeneous, invasive subpopulations of tumor cells. |
| TextSentencer_T13 |
1763-2026 |
Sentence |
denotes |
Moreover, increased cell-surface SSEA-4 expression is associated with the loss of cell-cell interactions and the gain of a migratory phenotype, suggesting an important role of SSEA-4 in cancer invasion by influencing cellular adhesion to the extracellular matrix. |
| T13 |
1763-2026 |
Sentence |
denotes |
Moreover, increased cell-surface SSEA-4 expression is associated with the loss of cell-cell interactions and the gain of a migratory phenotype, suggesting an important role of SSEA-4 in cancer invasion by influencing cellular adhesion to the extracellular matrix. |
| T13 |
1763-2026 |
Sentence |
denotes |
Moreover, increased cell-surface SSEA-4 expression is associated with the loss of cell-cell interactions and the gain of a migratory phenotype, suggesting an important role of SSEA-4 in cancer invasion by influencing cellular adhesion to the extracellular matrix. |