Metabolic changes of host cells in response to HBV replication

As a multifunctional regulator, HBx has long been suspected as the primary factor for inducing HCC. However, as a DNA virus, HBV exhibits relatively high mutation rate, thus studying the pathology of different genotypes of HBx mutants seems to be significant. GC/MS is utilized to qualitatively and q...

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Main Author: Li, Lingyu
Other Authors: Chen Wei Ning, William
Format: Thesis
Language:English
Published: 2012
Subjects:
Online Access:http://hdl.handle.net/10356/50533
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author Li, Lingyu
author2 Chen Wei Ning, William
author_facet Chen Wei Ning, William
Li, Lingyu
author_sort Li, Lingyu
collection NTU
description As a multifunctional regulator, HBx has long been suspected as the primary factor for inducing HCC. However, as a DNA virus, HBV exhibits relatively high mutation rate, thus studying the pathology of different genotypes of HBx mutants seems to be significant. GC/MS is utilized to qualitatively and quantitatively analyse the metabolites change of host cell in response to the introduction of HBx gene. Four kinds of metabolites are finally picked out: butanedioic acid, glutamine, lactic acid and D-glucose. The first two molecules are significantly down-regulated while the other two seem to be up-regulated, suggesting that glycolysis of the infected cells is enhanced, while TCAC activity is inhibited.
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spelling ntu-10356/505332023-03-03T16:01:36Z Metabolic changes of host cells in response to HBV replication Li, Lingyu Chen Wei Ning, William School of Chemical and Biomedical Engineering DRNTU::Engineering::Chemical engineering As a multifunctional regulator, HBx has long been suspected as the primary factor for inducing HCC. However, as a DNA virus, HBV exhibits relatively high mutation rate, thus studying the pathology of different genotypes of HBx mutants seems to be significant. GC/MS is utilized to qualitatively and quantitatively analyse the metabolites change of host cell in response to the introduction of HBx gene. Four kinds of metabolites are finally picked out: butanedioic acid, glutamine, lactic acid and D-glucose. The first two molecules are significantly down-regulated while the other two seem to be up-regulated, suggesting that glycolysis of the infected cells is enhanced, while TCAC activity is inhibited. Master of Science 2012-06-11T09:01:14Z 2012-06-11T09:01:14Z 2012 2012 Thesis http://hdl.handle.net/10356/50533 en 53 p. application/pdf
spellingShingle DRNTU::Engineering::Chemical engineering
Li, Lingyu
Metabolic changes of host cells in response to HBV replication
title Metabolic changes of host cells in response to HBV replication
title_full Metabolic changes of host cells in response to HBV replication
title_fullStr Metabolic changes of host cells in response to HBV replication
title_full_unstemmed Metabolic changes of host cells in response to HBV replication
title_short Metabolic changes of host cells in response to HBV replication
title_sort metabolic changes of host cells in response to hbv replication
topic DRNTU::Engineering::Chemical engineering
url http://hdl.handle.net/10356/50533
work_keys_str_mv AT lilingyu metabolicchangesofhostcellsinresponsetohbvreplication