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The biology of Hepatocellular carcinoma: implications for genomic and immune therapies
by
Khemlina, Galina
, Kurzrock, Razelle
, Ikeda, Sadakatsu
in
Analysis
/ Animals
/ Biomarkers, Tumor
/ Biomedical and Life Sciences
/ Biomedicine
/ Cancer genetics
/ Cancer Research
/ Carcinoma, Hepatocellular - etiology
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Transformation, Neoplastic - genetics
/ Cell Transformation, Neoplastic - metabolism
/ Gene Expression Regulation, Neoplastic
/ Gene mutation
/ Genetic aspects
/ Genetic Variation
/ Genomics - methods
/ Health aspects
/ Hepatocellular carcinoma
/ Humans
/ Immunohistochemistry
/ Immunotherapy
/ Immunotherapy - methods
/ Liver Neoplasms - etiology
/ Liver Neoplasms - metabolism
/ Liver Neoplasms - pathology
/ Liver Neoplasms - therapy
/ Molecular targeted therapyg
/ Next-generation sequencing
/ Oncology
/ Review
/ Signal Transduction
2017
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The biology of Hepatocellular carcinoma: implications for genomic and immune therapies
by
Khemlina, Galina
, Kurzrock, Razelle
, Ikeda, Sadakatsu
in
Analysis
/ Animals
/ Biomarkers, Tumor
/ Biomedical and Life Sciences
/ Biomedicine
/ Cancer genetics
/ Cancer Research
/ Carcinoma, Hepatocellular - etiology
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Transformation, Neoplastic - genetics
/ Cell Transformation, Neoplastic - metabolism
/ Gene Expression Regulation, Neoplastic
/ Gene mutation
/ Genetic aspects
/ Genetic Variation
/ Genomics - methods
/ Health aspects
/ Hepatocellular carcinoma
/ Humans
/ Immunohistochemistry
/ Immunotherapy
/ Immunotherapy - methods
/ Liver Neoplasms - etiology
/ Liver Neoplasms - metabolism
/ Liver Neoplasms - pathology
/ Liver Neoplasms - therapy
/ Molecular targeted therapyg
/ Next-generation sequencing
/ Oncology
/ Review
/ Signal Transduction
2017
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The biology of Hepatocellular carcinoma: implications for genomic and immune therapies
by
Khemlina, Galina
, Kurzrock, Razelle
, Ikeda, Sadakatsu
in
Analysis
/ Animals
/ Biomarkers, Tumor
/ Biomedical and Life Sciences
/ Biomedicine
/ Cancer genetics
/ Cancer Research
/ Carcinoma, Hepatocellular - etiology
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Transformation, Neoplastic - genetics
/ Cell Transformation, Neoplastic - metabolism
/ Gene Expression Regulation, Neoplastic
/ Gene mutation
/ Genetic aspects
/ Genetic Variation
/ Genomics - methods
/ Health aspects
/ Hepatocellular carcinoma
/ Humans
/ Immunohistochemistry
/ Immunotherapy
/ Immunotherapy - methods
/ Liver Neoplasms - etiology
/ Liver Neoplasms - metabolism
/ Liver Neoplasms - pathology
/ Liver Neoplasms - therapy
/ Molecular targeted therapyg
/ Next-generation sequencing
/ Oncology
/ Review
/ Signal Transduction
2017
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The biology of Hepatocellular carcinoma: implications for genomic and immune therapies
Journal Article
The biology of Hepatocellular carcinoma: implications for genomic and immune therapies
2017
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Overview
Hepatocellular carcinoma (HCC), the most common type of primary liver cancer, is a leading cause of cancer-related death worldwide. It is highly refractory to most systemic therapies. Recently, significant progress has been made in uncovering genomic alterations in HCC, including potentially targetable aberrations. The most common molecular anomalies in this malignancy are mutations in the
TERT
promoter,
TP53
,
CTNNB1
,
AXIN1
,
ARID1A, CDKN2A
and
CCND1
genes
.
PTEN loss at the protein level is also frequent. Genomic portfolios stratify by risk factors as follows: (i)
CTNNB1
with alcoholic cirrhosis; and (ii)
TP53
with hepatitis B virus-induced cirrhosis. Activating mutations in
CTNNB1
and inactivating mutations in
AXIN1
both activate WNT signaling. Alterations in this pathway, as well as in
TP53
and the cell cycle machinery, and in the PI3K/Akt/mTor axis (the latter activated in the presence of PTEN loss), as well as aberrant angiogenesis and epigenetic anomalies, appear to be major events in HCC. Many of these abnormalities may be pharmacologically tractable. Immunotherapy with checkpoint inhibitors is also emerging as an important treatment option. Indeed, 82% of patients express PD-L1 (immunohistochemistry) and response rates to anti-PD-1 treatment are about 19%, and include about 5% complete remissions as well as durable benefit in some patients. Biomarker-matched trials are still limited in this disease, and many of the genomic alterations in HCC remain challenging to target. Future studies may require combination regimens that include both immunotherapies and molecularly matched targeted treatments.
Publisher
BioMed Central,BioMed Central Ltd,BMC
Subject
/ Animals
/ Biomedical and Life Sciences
/ Carcinoma, Hepatocellular - etiology
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Carcinoma, Hepatocellular - therapy
/ Cell Transformation, Neoplastic - genetics
/ Cell Transformation, Neoplastic - metabolism
/ Gene Expression Regulation, Neoplastic
/ Humans
/ Liver Neoplasms - metabolism
/ Oncology
/ Review
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