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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Main Author: Muhammad Bakhait Rahmat.
Other Authors: School of Biological Sciences
Format: Final Year Project
Language:English
Published: 2013
Subjects:
Online Access:http://hdl.handle.net/10356/53800
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Institution: Nanyang Technological University
Language: English
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spelling 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
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic DRNTU::Science
spellingShingle DRNTU::Science
Muhammad Bakhait Rahmat.
Investigating the role of RUNX3 in Epithelial-Mesenchymal Transition (EMT).
description 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.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Muhammad Bakhait Rahmat.
format 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
url http://hdl.handle.net/10356/53800
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