Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT).
RUNX3 is a transcription factor known for its tumor suppressor activity, and more recently has been implicated in cancer metastasis. One of the factors involved in successful cancer metastasis is the acquisition of phenotypic plasticity for migration and re-colonization, a process known as Epithelia...
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sg-ntu-dr.10356-538002019-12-10T11:13:18Z Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT). Muhammad Bakhait Rahmat. School of Biological Sciences Madhura Kalkurni DRNTU::Science RUNX3 is a transcription factor known for its tumor suppressor activity, and more recently has been implicated in cancer metastasis. One of the factors involved in successful cancer metastasis is the acquisition of phenotypic plasticity for migration and re-colonization, a process known as Epithelial-mesenchymal transition (EMT). To elucidate the role of RUNX3 in EMT progression, RUNX3 expression in A549 cells was knocked down, and the progression of EMT stages was assessed and compared to that of control cells expressing endogenous RUNX3 after growth factor stimulation. Herein, we found that in the absence of RUNX3, mesenchymal markers were induced earlier and expressed higher than control cells. These findings indicate that RUNX3 possibly imparts an inhibitory effect in A549 cells undergoing EMT. Further biochemical studies need to be followed up to investigate the mechanistic principles involved in RUNX3 mediated inhibition of EMT in intermediate stage A549 cell lines. Bachelor of Science in Biological Sciences 2013-06-07T06:46:46Z 2013-06-07T06:46:46Z 2013 2013 Final Year Project (FYP) http://hdl.handle.net/10356/53800 en Nanyang Technological University 34 p. application/msword |
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DRNTU::Science Muhammad Bakhait Rahmat. Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT). |
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RUNX3 is a transcription factor known for its tumor suppressor activity, and more recently has been implicated in cancer metastasis. One of the factors involved in successful cancer metastasis is the acquisition of phenotypic plasticity for migration and re-colonization, a process known as Epithelial-mesenchymal transition (EMT). To elucidate the role of RUNX3 in EMT progression, RUNX3 expression in A549 cells was knocked down, and the progression of EMT stages was assessed and compared to that of control cells expressing endogenous RUNX3 after growth factor stimulation. Herein, we found that in the absence of RUNX3, mesenchymal markers were induced earlier and expressed higher than control cells. These findings indicate that RUNX3 possibly imparts an inhibitory effect in A549 cells undergoing EMT. Further biochemical studies need to be followed up to investigate the mechanistic principles involved in RUNX3 mediated inhibition of EMT in intermediate stage A549 cell lines. |
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School of Biological Sciences |
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School of Biological Sciences Muhammad Bakhait Rahmat. |
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Final Year Project |
author |
Muhammad Bakhait Rahmat. |
author_sort |
Muhammad Bakhait Rahmat. |
title |
Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT). |
title_short |
Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT). |
title_full |
Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT). |
title_fullStr |
Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT). |
title_full_unstemmed |
Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT). |
title_sort |
investigating the role of runx3 in epithelial-mesenchymal transition (emt). |
publishDate |
2013 |
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http://hdl.handle.net/10356/53800 |
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1681049254818217984 |