International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(13), P. 7377 - 7377
Published: July 5, 2024
Gastric
cancer
is
the
fifth
most
common
disease
in
world
and
fourth
cause
of
death.
It
diagnosed
through
esophagogastroduodenoscopy
with
biopsy;
however,
there
are
limitations
finding
lesions
early
stages.
Recently,
research
has
been
actively
conducted
to
use
liquid
biopsy
diagnose
various
cancers,
including
gastric
cancer.
Various
substances
derived
from
reflected
blood.
By
analyzing
these
substances,
it
was
expected
that
not
only
presence
or
absence
but
also
type
can
be
diagnosed.
However,
amount
extremely
small,
even
have
variables
depending
on
characteristics
individual
To
overcome
these,
we
collected
methylated
DNA
fragments
using
MeDIP
compared
them
normal
plasma
characterize
tissue
patients'
plasma.
We
attempted
blood
As
a
result,
confirmed
consistency
between
approximately
41.2%
found
possibility
diagnosing
characterizing
SFR
5'end-motif
analysis.
Cancer Science,
Journal Year:
2024,
Volume and Issue:
115(4), P. 1060 - 1072
Published: Feb. 3, 2024
Abstract
Liquid
biopsy
is
emerging
as
a
pivotal
tool
in
precision
oncology,
offering
noninvasive
and
comprehensive
approach
to
cancer
diagnostics
management.
By
harnessing
biofluids
such
blood,
urine,
saliva,
cerebrospinal
fluid,
pleural
effusions,
this
technique
profiles
key
biomarkers
including
circulating
tumor
DNA,
cells,
microRNAs,
extracellular
vesicles.
This
review
discusses
the
extended
scope
of
liquid
biopsy,
highlighting
its
indispensable
role
enhancing
patient
outcomes
through
early
detection,
continuous
monitoring,
tailored
therapy.
While
advantages
are
notable,
we
also
address
challenges,
emphasizing
necessity
for
precision,
cost‐effectiveness,
standardized
methodologies
broader
application.
The
future
trajectory
set
expand
reach
personalized
medicine,
fueled
by
technological
advancements
collaborative
research.
Medicine in Omics,
Journal Year:
2024,
Volume and Issue:
11, P. 100039 - 100039
Published: May 21, 2024
Over
the
last
few
years,
development
of
so-called
omics
technologies
has
greatly
contributed
to
discovery
new
biomarkers
and
targets,
embracing
various
fields
from
diagnostics
therapy
contributing
meliorate
advance
precision
personalized
medicine.
In
addition
classic
omics,
including
genomics,
transcriptomics,
proteomics,
metabolomics,
newer-generation
their
platforms,
such
as
microbiomics
nutrigenomics,
are
emerging.
parallel,
use
liquid
biopsies,
optimal
biological
samples,
consisting
in
fluids
(i.e.
blood,
saliva,
urine)
easy
collect,
whose
components
(cells,
nucleic
acids,
exosome)
can
be
analysed
using
throughput
techniques,
is
becoming
an
attractive,
because
enables
extrapolation
big
data
via
multi-omics
technologies.
Here,
we
report
a
brief
description
discussion
technologies,
by
evidencing
applications
eventual
limitations.
Journal of Molecular Neuroscience,
Journal Year:
2025,
Volume and Issue:
75(1)
Published: March 13, 2025
Abstract
Neurodegenerative
disorders,
including
Alzheimer’s
disease
(AD),
Parkinson’s
(PD),
multiple
sclerosis
(MS),
and
amyotrophic
lateral
(ALS),
are
characterized
by
the
progressive
gradual
degeneration
of
neurons.
The
prevalence
rates
these
disorders
rise
significantly
with
age.
As
life
spans
continue
to
increase
in
many
countries,
number
cases
is
expected
grow
foreseeable
future.
Early
precise
diagnosis,
along
appropriate
surveillance,
continues
pose
a
challenge.
high
heterogeneity
neurodegenerative
diseases
calls
for
more
accurate
definitive
biomarkers
improve
clinical
therapy.
Cell-free
DNA
(cfDNA),
fragmented
released
into
bodily
fluids
via
apoptosis,
necrosis,
or
active
secretion,
has
emerged
as
promising
non-invasive
diagnostic
tool
various
diseases.
cfDNA
can
serve
an
indicator
ongoing
cellular
damage
mortality,
neuronal
loss,
may
provide
valuable
insights
processes,
progression,
therapeutic
responses.
This
review
will
first
cover
key
aspects
then
examine
recent
advances
its
potential
use
biomarker
disorders.
IEEE Journal of Translational Engineering in Health and Medicine,
Journal Year:
2024,
Volume and Issue:
12, P. 306 - 313
Published: Jan. 1, 2024
Objective
:
The
field
of
cancer
diagnostics
has
been
revolutionized
by
liquid
biopsies,
which
offer
a
bridge
between
laboratory
research
and
clinical
settings.
These
tests
are
less
invasive
than
traditional
biopsies
more
convenient
routine
imaging
methods.
Liquid
allow
studying
tumor-derived
markers
in
bodily
fluids,
enabling
the
development
precise
diagnostic
for
screening,
disease
monitoring,
therapy
personalization.
This
study
presents
multiclass
approach
based
on
deep
learning
to
analyze
classify
diseases
blood
platelet
RNA.
Its
primary
objective
is
enhance
cancer-type
diagnosis
settings
leveraging
power
combined
with
high-throughput
sequencing
biopsy.
Ultimately,
demonstrates
potential
this
accurately
identify
patient's
type
cancer.
xmlns:xlink="http://www.w3.org/1999/xlink">Methods
developed
method
classifies
patients
using
heatmap
images,
generated
gene
expression
arranged
according
Kyoto
Encyclopedia
Genes
Genomes
pathways.
images
represent
samples
ovarian
cancer,
endometrial
glioblastoma,
non-small
cell
lung
sarcoma,
as
well
brain
metastasis.
xmlns:xlink="http://www.w3.org/1999/xlink">Results
Our
learning-based
models
reached
66.51%
balanced
accuracy
when
distinguishing
those
6
sites
origin
90.5%
location-specific
dataset
where
types
from
close
locations
were
grouped.
further
investigated
an
explainable
artificial
intelligence-based
(XAI)
-SHAP.
They
returned
set
60
genes
highest
impact
models'
decision-making
process.
xmlns:xlink="http://www.w3.org/1999/xlink">Conclusions
results
show
that
deep-learning
methods
promising
opportunity
detection
could
support
clinicians'
process
finding
solution
black-box
problem.
Biomedical Journal,
Journal Year:
2024,
Volume and Issue:
unknown, P. 100718 - 100718
Published: March 1, 2024
This
review
provides
a
comprehensive
overview
of
the
latest
advancements
in
clinical
utility
liquid
biopsy,
with
particular
focus
on
epigenetic
approaches
aimed
at
overcoming
challenges
cancer
diagnosis
and
treatment.
It
begins
by
elucidating
key
terms,
including
methylomics,
fragmentomics,
nucleosomics.
The
progresses
to
discuss
methods
for
analyzing
circulating
cell-free
DNA
(cfDNA)
highlights
recent
studies
showcasing
relevance
modifications
areas
such
as
diagnosis,
drug
treatment
response,
minimal
residual
disease
(MRD)
detection,
prognosis
prediction.
While
acknowledging
hurdles
like
complexity
interpreting
data
absence
standardization,
charts
path
forward.
advocates
integration
multi-omic
through
machine
learning
algorithms
refine
predictive
models
stresses
importance
collaboration
among
clinicians,
researchers,
scientists.
Such
cooperative
efforts
are
essential
fully
leverage
potential
features
practice.
Cancer Letters,
Journal Year:
2024,
Volume and Issue:
unknown, P. 217350 - 217350
Published: Nov. 1, 2024
Pancreatic
cancer
remains
one
of
the
most
challenging
malignancies
to
treat
due
its
late-stage
diagnosis,
aggressive
progression,
and
high
resistance
existing
therapies.
This
review
examines
latest
advancements
in
early
detection,
therapeutic
strategies,
with
a
focus
on
emerging
biomarkers,
tumor
microenvironment
(TME)
modulation,
integration
artificial
intelligence
(AI)
data
analysis.
We
highlight
promising
including
microRNAs
(miRNAs)
circulating
DNA
(ctDNA),
that
offer
enhanced
sensitivity
specificity
for
early-stage
diagnosis
when
combined
multi-omics
panels.
A
detailed
analysis
TME
reveals
how
components
such
as
cancer-associated
fibroblasts
(CAFs),
immune
cells,
extracellular
matrix
(ECM)
contribute
therapy
by
creating
immunosuppressive
barriers.
also
discuss
interventions
target
these
components,
aiming
improve
drug
delivery
overcome
evasion.
Furthermore,
AI-driven
analyses
are
explored
their
potential
interpret
complex
data,
enabling
personalized
treatment
strategies
real-time
monitoring
response.
conclude
identifying
key
areas
future
research,
clinical
validation
regulatory
frameworks
AI
applications,
equitable
access
innovative
comprehensive
approach
underscores
need
integrated,
outcomes
pancreatic
cancer.
Frontiers in Genetics,
Journal Year:
2024,
Volume and Issue:
15
Published: Jan. 18, 2024
Vascular
malformations
are
congenital
lesions
that
occur
due
to
mutations
in
major
cellular
signalling
pathways
which
govern
angiogenesis,
cell
proliferation,
motility,
and
death.
These
have
been
widely
studied
oncology
substrates
for
various
small
molecule
inhibitors.
Given
their
common
molecular
biology,
there
is
now
a
potential
repurpose
these
cancer
drugs
vascular
malformation
care;
however,
diagnosis
required
order
tailour
specific
the
individual
patient’s
mutational
profile.
Liquid
biopsies
(LBs),
emerging
as
transformative
tool
field
of
oncology,
hold
significant
promise
this
feat.
This
paper
explores
principles
technologies
underlying
LBs
evaluates
revolutionize
management
malformations.
The
review
begins
by
delineating
fundamental
LBs,
focusing
on
detection
analysis
circulating
biomarkers
such
cell-free
DNA,
tumor
cells,
extracellular
vesicles.
Subsequently,
an
in-depth
technological
advancements
driving
LB
platforms
presented.
Lastly,
highlights
current
state
research
applying
malformations,
uses
aforementioned
techniques
conceptualize
liquid
biopsy
framework
unique
clinical
care.
International Journal of Molecular Sciences,
Journal Year:
2025,
Volume and Issue:
26(5), P. 2216 - 2216
Published: Feb. 28, 2025
Colorectal
cancer
(CRC)
remains
a
leading
cause
of
cancer-related
mortality,
with
metastatic
disease
posing
significant
therapeutic
challenges.
While
anti-EGFR
therapy
has
improved
outcomes
for
patients
RAS
and
BRAF
wild-type
tumors,
resistance
major
hurdle,
limiting
treatment
efficacy.
The
concept
negative
hyperselection
emerged
as
refinement
molecular
profiling,
identifying
additional
genomic
alterations-such
HER2
MET
amplificationsand
MAP2K1
mutations-that
predict
to
agents.
Studies
incorporating
these
expanded
assessments
have
demonstrated
that
nearly
half
RAS/BRAF
tumors
harbor
alternative
biomarkers,
underscoring
the
need
selection
criteria.
Liquid
biopsies,
particularly
circulating
tumor
DNA
(ctDNA)
analysis,
revolutionized
precision
oncology
by
providing
minimally
invasive,
real-time
assessment
dynamics.
ctDNA-based
enables
detection
resistance-associated
alterations,
guiding
decisions
greater
accuracy
than
conventional
tissue
biopsies.
Recent
trials
support
predictive
value
ctDNA-defined
hyperselection,
revealing
superior
stratified
through
liquid
biopsy.
This
narrative
review
explores
evolving
role
in
first-line
therapy,
emphasizing
integration
ctDNA
refine
patient
selection,
enhance
efficacy,
pave
way
personalized
strategies
CRC.
World Journal of Gastrointestinal Oncology,
Journal Year:
2025,
Volume and Issue:
17(4)
Published: March 24, 2025
A
recent
study
by
Long
et
al
used
a
predictive
model
to
explore
the
efficacy
of
radiomics
based
on
multiparametric
magnetic
resonance
imaging
in
predicting
metachronous
liver
metastasis
(MLM)
newly
diagnosed
rectal
cancer
(RC)
patients.
The
machine
learning
algorithms,
particularly
random
forest
(RFM),
appeared
well-matched
complex
nature
data.
capabilities
RFM,
as
evidenced
area
under
curve
0.919
training
cohort
and
0.901
validation
cohort,
highlighted
its
potential
clinical
utility.
However,
we
several
methodological
limitations,
including
excluding
genomic
markers,
biases
from
retrospective
design,
limited
generalizability
due
single-center
study,
variability
image
interpretation.
We
propose
further
investigation
into
integrating
multi-omic
data,
conducting
larger
multicenter
studies,
utilizing
advanced
techniques.
Additionally,
importance
interdisciplinary
collaboration
improve
development
advocate
for
cost-effectiveness
analyses
facilitate
integration.
Overall,
this
may
early
detection
management
MLM
RC
patients,
with
promising
avenues
future
exploration.
Ongoing
research
domain
can
potentially
outcomes
quality
care