Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection.

Hepatitis B virus (HBV) infection is a major risk factor for hepatocellular carcinoma (HCC). Antiviral drug therapy used to treat Chronic Hepatitis B patients at high risk of developing HCC has resulted in drug-resistant HBV mutants, which may lead to a different onset mechanism to HCC. Early detect...

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Main Author: Lee, Kar Kei.
Other Authors: Chen Wei Ning, William
Format: Final Year Project
Language:English
Published: 2010
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Online Access:http://hdl.handle.net/10356/40195
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-401952023-03-03T15:36:16Z Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection. Lee, Kar Kei. Chen Wei Ning, William School of Chemical and Biomedical Engineering DRNTU::Science::Medicine::Biosensors Hepatitis B virus (HBV) infection is a major risk factor for hepatocellular carcinoma (HCC). Antiviral drug therapy used to treat Chronic Hepatitis B patients at high risk of developing HCC has resulted in drug-resistant HBV mutants, which may lead to a different onset mechanism to HCC. Early detection of HBV-HCC is crucial to the patient’s recovery. However, to date, much of the researches only focused on developing biomarkers for wild-type HBV induced HCC. This research addresses the need to also develop biomarkers for early diagnosis of mutant HBV induced HCC. As a small digression, the research also looked into the possibility of interaction between Hepatitis B x protein (HBx) with Siah1 protein (which plays a role in inducing apoptosis) to establish evidence for HBx as a potential drug target. The research focuses on designing experiment approaches for biomarker discovery and binding mechanism identification. For biomarker discovery, iTRAQ coupled 2D-liquid chromatography-mass spectrometry was chosen as the method to study the protein profiles of different HBV strains induced HCC. Meanwhile, for the HBx-Siah1 interaction, a Siah1 binding motif-like structure was found in HBx from previous studies. To validate the actual binding, fusion protein plasmid constructs of HBx and Siah1 would be used to transfect HepG2 cells. In-vivo binding of the proteins is then confirmed using an anti-HA-Sepharose pull-down assay. Overall, the proposed experiments were anticipated to give potentially useful results for early diagnosis of HBV induced HCC and also reinforcing the prospect of HBx as drug target. Future implementation of the experiments should consider large scale population studies to verify the results. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2010-06-11T05:08:42Z 2010-06-11T05:08:42Z 2010 2010 Final Year Project (FYP) http://hdl.handle.net/10356/40195 en Nanyang Technological University 67 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Medicine::Biosensors
spellingShingle DRNTU::Science::Medicine::Biosensors
Lee, Kar Kei.
Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection.
description Hepatitis B virus (HBV) infection is a major risk factor for hepatocellular carcinoma (HCC). Antiviral drug therapy used to treat Chronic Hepatitis B patients at high risk of developing HCC has resulted in drug-resistant HBV mutants, which may lead to a different onset mechanism to HCC. Early detection of HBV-HCC is crucial to the patient’s recovery. However, to date, much of the researches only focused on developing biomarkers for wild-type HBV induced HCC. This research addresses the need to also develop biomarkers for early diagnosis of mutant HBV induced HCC. As a small digression, the research also looked into the possibility of interaction between Hepatitis B x protein (HBx) with Siah1 protein (which plays a role in inducing apoptosis) to establish evidence for HBx as a potential drug target. The research focuses on designing experiment approaches for biomarker discovery and binding mechanism identification. For biomarker discovery, iTRAQ coupled 2D-liquid chromatography-mass spectrometry was chosen as the method to study the protein profiles of different HBV strains induced HCC. Meanwhile, for the HBx-Siah1 interaction, a Siah1 binding motif-like structure was found in HBx from previous studies. To validate the actual binding, fusion protein plasmid constructs of HBx and Siah1 would be used to transfect HepG2 cells. In-vivo binding of the proteins is then confirmed using an anti-HA-Sepharose pull-down assay. Overall, the proposed experiments were anticipated to give potentially useful results for early diagnosis of HBV induced HCC and also reinforcing the prospect of HBx as drug target. Future implementation of the experiments should consider large scale population studies to verify the results.
author2 Chen Wei Ning, William
author_facet Chen Wei Ning, William
Lee, Kar Kei.
format Final Year Project
author Lee, Kar Kei.
author_sort Lee, Kar Kei.
title Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection.
title_short Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection.
title_full Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection.
title_fullStr Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection.
title_full_unstemmed Smart detectives for early detection of hepatocellular carcinoma related to drug-resistant HBV-mutant infection.
title_sort smart detectives for early detection of hepatocellular carcinoma related to drug-resistant hbv-mutant infection.
publishDate 2010
url http://hdl.handle.net/10356/40195
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