Journal of Translational Medicine,
Год журнала:
2024,
Номер
22(1)
Опубликована: Март 15, 2024
Abstract
Background
Ovarian
cancer
(OC)
is
distinguished
by
its
aggressive
nature
and
the
limited
efficacy
of
current
treatment
strategies.
Recent
studies
have
emphasized
significant
role
cancer-associated
fibroblasts
(CAFs)
in
OC
development
progression.
Methods
Employing
sophisticated
machine
learning
techniques
on
bulk
transcriptomic
datasets,
we
identified
fibroblast
growth
factor
7
(FGF7),
derived
from
CAFs,
as
a
potential
oncogenic
factor.
We
investigated
relationship
between
FGF7
expression
various
clinical
parameters.
A
series
vitro
experiments
were
undertaken
to
evaluate
effect
CAFs-derived
cell
activities,
such
proliferation,
migration,
invasion.
Single-cell
analysis
was
also
conducted
elucidate
interaction
receptor.
Detailed
mechanistic
investigations
sought
clarify
pathways
through
which
fosters
Results
Our
findings
indicate
that
higher
levels
correlate
with
advanced
tumor
stages,
increased
vascular
invasion,
poorer
prognosis.
significantly
enhanced
revealed
inhibits
ubiquitination
degradation
hypoxia-inducible
1
alpha
(HIF-1α)
via
FGFR2
interaction.
Activation
FGF7/HIF-1α
pathway
resulted
upregulation
mesenchymal
markers
downregulation
epithelial
markers.
Importantly,
vivo
neutralizing
antibodies
targeting
substantially
reduced
growth.
Conclusion
Neutralizing
medium
or
inhibiting
HIF-1α
signaling
reversed
effects
FGF7-mediated
EMT,
emphasizing
dependence
EMT
activation.
These
suggest
FGF7/HIF-1α/EMT
axis
may
offer
new
therapeutic
opportunities
intervene
Nucleic Acids Research,
Год журнала:
2024,
Номер
52(W1), С. W415 - W421
Опубликована: Май 29, 2024
Enrichment
analysis,
crucial
for
interpreting
genomic,
transcriptomic,
and
proteomic
data,
is
expanding
into
metabolomics.
Furthermore,
there
a
rising
demand
integrated
enrichment
analysis
that
combines
data
from
different
studies
omics
platforms,
as
seen
in
meta-analysis
multi-omics
research.
To
address
these
growing
needs,
we
have
updated
WebGestalt
to
include
capabilities
both
metabolites
multiple
input
lists
of
analytes.
We
also
significantly
increased
speed,
revamped
the
user
interface,
introduced
new
pathway
visualizations
accommodate
updates.
Notably,
adoption
Rust
backend
reduced
gene
set
time
by
95%
270.64
12.41
s
network
topology-based
89%
159.59
17.31
our
evaluation.
This
performance
improvement
accessible
R
package
newly
Python
package.
Additionally,
database
reflect
current
status
each
source
expanded
collection
pathways,
networks,
signatures.
The
2024
update
represents
significant
leap
forward,
offering
support
metabolomics,
streamlined
capabilities,
remarkable
enhancements.
Discover
updates
more
at
https://www.webgestalt.org.
Frontiers in Artificial Intelligence,
Год журнала:
2023,
Номер
6
Опубликована: Фев. 9, 2023
Biological
systems
function
through
complex
interactions
between
various
'omics
(biomolecules),
and
a
more
complete
understanding
of
these
is
only
possible
an
integrated,
multi-omic
perspective.
This
has
presented
the
need
for
development
integration
approaches
that
are
able
to
capture
complex,
often
non-linear,
define
biological
adapted
challenges
combining
heterogenous
data
across
'omic
views.
A
principal
challenge
missing
because
all
biomolecules
not
measured
in
samples.
Due
either
cost,
instrument
sensitivity,
or
other
experimental
factors,
sample
may
be
one
techologies.
Recent
methodological
developments
artificial
intelligence
statistical
learning
have
greatly
facilitated
analyses
multi-omics
data,
however
many
techniques
assume
access
completely
observed
data.
subset
methods
incorporate
mechanisms
handling
partially
samples,
focus
this
review.
We
describe
recently
developed
approaches,
noting
their
primary
use
cases
highlighting
each
method's
approach
additionally
provide
overview
traditional
workflows
limitations;
we
discuss
potential
avenues
further
as
well
how
issue
its
current
solutions
generalize
beyond
context.
Machine
learning
(ML)
methods
are
motivated
by
the
need
to
automate
information
extraction
from
large
datasets
in
order
support
human
users
data-driven
tasks.
This
is
an
attractive
approach
for
integrative
joint
analysis
of
vast
amounts
omics
data
produced
next
generation
sequencing
and
other
-omics
assays.
A
systematic
assessment
current
literature
can
help
identify
key
trends
potential
gaps
methodology
applications.
We
surveyed
on
ML
multi-omic
integration
quantitatively
explored
goals,
techniques
involved
this
field.
were
particularly
interested
examining
how
researchers
use
deal
with
volume
complexity
these
datasets.Our
main
finding
that
used
those
address
challenges
few
samples
many
features.
Dimensionality
reduction
reduce
feature
count
alongside
models
also
appropriately
handle
relatively
samples.
Popular
include
autoencoders,
random
forests
vector
machines.
found
field
heavily
influenced
The
Cancer
Genome
Atlas
dataset,
which
accessible
contains
diverse
experiments.All
processing
scripts
available
at
GitLab
repository:
https://gitlab.com/polavieja_lab/ml_multi-omics_review/
or
Zenodo:
https://doi.org/10.5281/zenodo.7361807.Supplementary
Bioinformatics
online.
Biomedicines,
Год журнала:
2024,
Номер
12(7), С. 1496 - 1496
Опубликована: Июль 5, 2024
The
field
of
multi-omics
has
witnessed
unprecedented
growth,
converging
multiple
scientific
disciplines
and
technological
advances.
This
surge
is
evidenced
by
a
more
than
doubling
in
publications
within
just
two
years
(2022-2023)
since
its
first
referenced
mention
2002,
as
indexed
the
National
Library
Medicine.
emerging
demonstrated
capability
to
provide
comprehensive
insights
into
complex
biological
systems,
representing
transformative
force
health
diagnostics
therapeutic
strategies.
However,
several
challenges
are
evident
when
merging
varied
omics
data
sets
methodologies,
interpreting
vast
dimensions,
streamlining
longitudinal
sampling
analysis,
addressing
ethical
implications
managing
sensitive
information.
review
evaluates
these
while
spotlighting
pivotal
milestones:
development
targeted
methods,
use
artificial
intelligence
formulating
indices,
integration
sophisticated
Computational and Structural Biotechnology Journal,
Год журнала:
2024,
Номер
23, С. 2798 - 2810
Опубликована: Июнь 29, 2024
The
widespread
use
of
high-throughput
sequencing
technologies
has
revolutionized
the
understanding
biology
and
cancer
heterogeneity.
Recently,
several
machine-learning
models
based
on
transcriptional
data
have
been
developed
to
accurately
predict
patients'
outcome
clinical
response.
However,
an
open-source
R
package
covering
state-of-the-art
algorithms
for
user-friendly
access
yet
be
developed.
Thus,
we
proposed
a
flexible
computational
framework
construct
machine
learning-based
integration
model
with
elegant
performance
(Mime).
Mime
streamlines
process
developing
predictive
high
accuracy,
leveraging
complex
datasets
identify
critical
genes
associated
prognosis.
An
in
silico
combined
de
novo
PIEZO1-associated
signatures
constructed
by
demonstrated
accuracy
predicting
outcomes
patients
compared
other
published
models.
Furthermore,
could
also
precisely
infer
immunotherapy
response
applying
different
Mime.
Finally,
SDC1
selected
from
potential
as
glioma
target.
Taken
together,
our
provides
solution
constructing
will
greatly
expanded
provide
valuable
insights
into
current
fields.
is
available
GitHub
(https://github.com/l-magnificence/Mime).
Circulation Research,
Год журнала:
2024,
Номер
134(7), С. 842 - 854
Опубликована: Март 28, 2024
BACKGROUND:
Consistent
evidence
suggests
diabetes-protective
effects
of
dietary
fiber
intake.
However,
the
underlying
mechanisms,
particularly
role
gut
microbiota
and
host
circulating
metabolites,
are
not
fully
understood.
We
aimed
to
investigate
metabolites
associated
with
intake
their
relationships
type
2
diabetes
(T2D).
METHODS:
This
study
included
up
11
394
participants
from
HCHS/SOL
(Hispanic
Community
Health
Study/Study
Latinos).
Diet
was
assessed
two
24-hour
recalls
at
baseline.
examined
associations
microbiome
measured
by
shotgun
metagenomics
(350
species/85
genera
1958
enzymes;
n=2992
visit
2),
serum
metabolome
untargeted
metabolomics
(624
metabolites;
n=6198
baseline),
between
fiber-related
bacteria
(n=804
2).
prospective
microbial-associated
(n=3579
baseline)
incident
T2D
over
6
years.
RESULTS:
identified
multiple
bacterial
genera,
species,
related
enzymes
Several
(eg,
Butyrivibrio
,
Faecalibacterium
)
involved
in
degradation
xylanase
EC3.2.1.156)
were
positively
intake,
inversely
prevalent
T2D,
favorably
T2D-related
metabolic
traits.
159
47
which
T2D.
18
these
bacteria,
including
several
microbial
indolepropionate
3-phenylpropionate)
risk
Both
favorable
metabolites.
The
especially
attenuated
after
further
adjustment
for
CONCLUSIONS:
Among
United
States
Hispanics/Latinos,
profiles
These
findings
advance
our
understanding
relationship
diet