Two teams of Asian researchers have independently
completed whole-genome sequencing studies of a type of liver cancer commonly
caused by hepatitis virus infection.
Two
teams of Asian researchers, one Japanese and the other from China and
Singapore, have independently completed large-scale, whole-genome sequencing
studies of a type of liver cancer commonly caused by hepatitis B virus (HBV)
and hepatitis C virus (HCV) infection.
Both
studies were published this week in Nature Genetics, providing
important insights into how hepatitis viral infection causes hepatocellular
carcinoma (HCC), the most common form of liver cancer worldwide, and may lead
to improvements in diagnosis and treatment.
Individuals
infected with HBV and HCV are known to have a significantly higher risk of
developing HCC.
In
countries like China and other parts of Asia where hepatitis B is endemic, HBV
infection is the predominant cause of HCC.
In
Japan, which has the highest HCC rates of any industrialized country in the
world, HCV infection is thought to be responsible for the majority of cases.
It is
thought that the HBV and HCV genomes are integrated into the genome of the
human host in a manner that promotes the accumulation of genetic abnormalities,
leading to cancer development.
The
China-Singapore team studied tumor samples and adjacent normal tissues from 81
HBV-positive and 7 HBV-negative HCC patients while the Japanese team collected
tumor and blood samples from 11 HBV-positive HCCs, 14 HCV-positive HCCs, and 2
HCCs that were not associated with hepatitis infection.
Both
teams used whole-genome sequencing technologies to identify novel gene
mutations that may be responsible for HCC development and pinpoint locations
where the viral genome has been integrated into the host genome.
In
particular, the China-Singapore team identified characteristics of HBV
integrations that may help the virus to control specific genes in the host
tumor, providing new insights into the mechanisms through which HBV integration
promotes cancer.
“A deep
understanding of the recurring HBV insertions in HCC will help the research
community identify novel molecular targets in liver cancer, for which effective
treatments are still limited,” said John Luk, a leader of the China-Singapore
collaboration.
The
articles can be found at: Fujimoto et al. (2012) Whole-genome Sequencing Of Liver Cancers
Identifies Etiological Influences On Mutation Patterns And Recurrent Mutations
In Chromatin Regulators and Sung et al. (2012) Genome-wide Survey Of Recurrent HBV
Integration In Hepatocellular Carcinoma.
Copyright:
Asian Scientist Magazine. Sources: BGI, Nature
Publishing Group.
No comments:
Post a Comment