Journal of Personalized Medicine,
Journal Year:
2022,
Volume and Issue:
12(8), P. 1247 - 1247
Published: July 29, 2022
Recent
years
have
witnessed
the
advent
of
molecular
profiling
for
intrahepatic
cholangiocarcinoma
(iCCA),
and
new
techniques
led
to
identification
several
alterations.
Precision
oncology
approaches
been
widely
evaluated
are
currently
under
assessment,
as
shown
by
recent
development
a
wide
range
agents
targeting
Fibroblast
Growth
Factor
Receptor
(FGFR)
2,
Isocitrate
Dehydrogenase
1
(IDH-1),
BRAF.
However,
knowledge
gaps
persist
in
understanding
genomic
landscape
this
hepatobiliary
malignancy.In
current
study,
we
aimed
comprehensively
analyze
clinicopathological
features
BAP1-mutated
iCCA
patients
public
datasets
increase
on
biological
profile
iCCA.The
database
including
772
iCCAs,
identified
BAP1
mutations
120
cases
(15.7%).
According
our
analysis,
no
differences
terms
overall
survival
relapse-free
were
observed
between
wild-type
receiving
radical
surgery.
In
addition,
IDH1,
PBRM1,
ARID1A
most
commonly
co-altered
genes
iCCAs.The
characterization
is
destined
become
increasingly
important,
more
efforts
implement
genomics
analysis
warranted.
The Oncologist,
Journal Year:
2024,
Volume and Issue:
unknown
Published: June 6, 2024
Abstract
Background
Patients
with
intrahepatic
cholangiocarcinoma
(ICC)
are
prone
to
recurrence
and
poor
survival.
Targeted
therapy
related
isocitrate
dehydrogenase
(IDH)
is
an
extremely
important
treatment.
IDH1
IDH2
mutations
generally
thought
have
similar
effects
on
the
tumor
landscape.
However,
it
doubtful
whether
these
2
exactly
same
cells
microenvironment.
Methods
All
collected
samples
were
subjected
simultaneous
whole-exon
sequencing
proteome
sequencing.
Results
accounted
for
12.2%,
5.5%,
all
missense
mutations.
Tumors
IDH
had
lower
proportions
of
KRAS
TP53
Mutated
genes
obviously
enriched
in
kinase
pathway
tumors
The
signaling
pathways
mainly
activation
cellular
metabolic
activities
increase
inhibitory
immune
Moreover,
unique
enrichment
DNA
repair
mutants
secretion
biological
molecules
mutants.
Inhibitory
might
be
more
prominent
mutants,
expression
checkpoints
PVR
HLA-DQB1
was
metabolism-related
inflammation-immune
response
clusters,
some
belonged
replication
cluster.
Conclusions
These
results
revealed
differential
mutation-related
landscapes,
we
provided
reference
database
guide
ICC
Expert Review of Gastroenterology & Hepatology,
Journal Year:
2024,
Volume and Issue:
18(10), P. 605 - 630
Published: Oct. 2, 2024
Introduction
After
years
of
treatment
stagnation
in
biliary
tract
cancers
(BTC),
there
has
been
a
notable
shift
with
the
emergence
targeted
therapies
and
immunotherapy,
leading
to
substantial
progress
tackling
this
aggressive
disease.
Journal of Personalized Medicine,
Journal Year:
2022,
Volume and Issue:
12(8), P. 1247 - 1247
Published: July 29, 2022
Recent
years
have
witnessed
the
advent
of
molecular
profiling
for
intrahepatic
cholangiocarcinoma
(iCCA),
and
new
techniques
led
to
identification
several
alterations.
Precision
oncology
approaches
been
widely
evaluated
are
currently
under
assessment,
as
shown
by
recent
development
a
wide
range
agents
targeting
Fibroblast
Growth
Factor
Receptor
(FGFR)
2,
Isocitrate
Dehydrogenase
1
(IDH-1),
BRAF.
However,
knowledge
gaps
persist
in
understanding
genomic
landscape
this
hepatobiliary
malignancy.In
current
study,
we
aimed
comprehensively
analyze
clinicopathological
features
BAP1-mutated
iCCA
patients
public
datasets
increase
on
biological
profile
iCCA.The
database
including
772
iCCAs,
identified
BAP1
mutations
120
cases
(15.7%).
According
our
analysis,
no
differences
terms
overall
survival
relapse-free
were
observed
between
wild-type
receiving
radical
surgery.
In
addition,
IDH1,
PBRM1,
ARID1A
most
commonly
co-altered
genes
iCCAs.The
characterization
is
destined
become
increasingly
important,
more
efforts
implement
genomics
analysis
warranted.