BME Frontiers,
Journal Year:
2024,
Volume and Issue:
6
Published: Jan. 13, 2024
Spatial
monoomics
has
been
recognized
as
a
powerful
tool
for
exploring
life
sciences.
Recently,
spatial
multiomics
advanced
considerably,
which
could
contribute
to
clarifying
many
biological
issues.
techniques
in
epigenomics,
genomics,
transcriptomics,
proteomics,
and
metabolomics
can
enhance
our
understanding
of
functions
cellular
identities
by
simultaneously
measuring
tissue
structures
biomolecule
levels.
technology
evolved
from
multiomics.
Moreover,
the
resolution,
high-throughput
detection
capability,
capture
efficiency,
compatibility
with
various
sample
types
omics
have
considerably
advanced.
Despite
technological
advances
this
field,
data
analysis
frameworks
stagnated.
Current
challenges
include
incomplete
pipeline,
overly
complex
tasks,
few
established
strategies.
In
review,
we
systematically
summarize
recent
developments
improvements
related
pipeline.
On
basis
technology,
propose
integration
strategy
cross-platform,
cross-slice,
cross-modality.
We
potential
applications
aiming
provide
researchers
clinicians
better
how
such
is
expected
substantially
impact
biology
precision
medicine
through
measurements
extraction
biomolecular
features.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
15
Published: March 26, 2025
Objective
The
metabolism
of
amino
acids
and
derivatives
(MAAD)
is
closely
related
to
the
occurrence
development
colorectal
cancer
(CRC),
but
specific
regulatory
mechanisms
are
not
yet
clear.
This
study
aims
explore
role
MAAD
in
progression
ultimately
identify
key
molecules
that
may
become
potential
therapeutic
targets
for
CRC.
Methods
integrates
bulk
transcriptome
single-cell
analyze
MAAD-related
genes
from
multiple
levels.
Subsequently,
numerous
machine
learning
methods
were
incorporated
construct
prognostic
models,
infiltration
immune
cells,
tumor
heterogeneity,
mutation
burden,
pathway
changes
under
different
modes
analyzed.
Finally,
identified
experimental
validation.
Results
We
successfully
constructed
models
Nomograms
based
on
molecules.
There
was
a
notable
survival
benefit
observed
low-risk
patients
when
contrasted
with
their
high-risk
counterparts.
In
addition,
group
had
poorer
response
immunotherapy
stronger
heterogeneity
compared
group.
Further
research
found
by
knocking
down
gene.
LSM8,
malignant
characteristics
cell
lines
significantly
alleviated,
suggesting
LSM8
target.
Conclusion
gene
likely
involved
CRC
could
be
hopeful
target
intervention.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: April 1, 2025
Lactylation
modification
is
postulated
to
influence
the
progression
of
heart
failure
(HF)
through
diverse
pathways,
albeit
underlying
mechanisms
remain
elusive.
Methods
In
this
study,
bioinformatics
approaches
were
employed
analyze
HF
dataset
(GSE5406)
retrieved
from
Gene
Expression
Omnibus,
with
objective
identifying
lactylation-related
genes
(LRGs).
Key
LRGs
implicated
in
selected
using
Least
Absolute
Shrinkage
and
Selection
Operator
(LASSO)
Weighted
Co-Expression
Network
Analysis
(WGCNA).
The
diagnostic
efficacy
biological
significance
these
evaluated
receiver
operating
characteristic
(ROC)
curve
analysis,
Set
Enrichment
Analysis,
immune
cell
infiltration
analysis.
Furthermore,
findings
validated
single-cell
sequencing
datasets
(GSE161470)
vitro
models
ascertain
expression
patterns
functional
roles
identified
key
LRGs.
A
total
276
dataset.
Initial
screening
utilizing
two
analysis
methods
pinpointed
BRD4
as
a
potential
pivotal
LRG
influencing
progression.
ROC
revealed
high
accuracy
for
BRD4,
an
Area
Under
Curve
score
0.877.
Immune
data
analyses
indicated
that
exhibits
strong
association
cells,
including
mast
T
macrophages,
demonstrates
significantly
elevated
cells
well
cardiomyocytes.
Both
mRNA
protein
levels
found
be
upregulated
compared
control
groups.
This
study
represents
first
utilize
multiple
identify
HF,
thereby
establishing
foundation
future
investigations
into
acylation-related
HF.
Annals of Medicine,
Journal Year:
2025,
Volume and Issue:
57(1)
Published: April 2, 2025
CcRCC
has
the
characteristics
of
high
aggression,
metastasis,
mortality,
wide
tumour
heterogeneity
and
variable
clinical
course.
The
purpose
this
study
was
to
explore
potential
value
lncRNAs-related
DNA
damage
repair
(DDR)
in
predicting
prognosis
ccRCC
by
construction
verification
a
novel
prognostic
model.
RNA-seq
data
were
downloaded
from
public
databases.
Subsequently,
Pearson
correlation
analysis
differential
expression
performed
identify
DElncRNAs-related
DDR.
Then,
through
univariate
Cox
LASSO
analysis,
DDR
associated
with
screened
for
risk
score
In
addition,
functional
annotation,
mutation
burden,
immune
drug
sensitivity
analyses
based
on
assess
patients
different
groups.
Based
four
best
selected.
model
these
DElncRNAs
constructed
LASSO.
Multivariate
showed
that
age
independent
factors
(p
<
0.05).
Functional
enrichment
DDR-related
biological
processes
mainly
enriched
group.
highly
mutated
genes
low
groups
same
(VHL,
PBRM1
TTN),
but
they
also
had
their
own
unique
genes.
significantly
0.05)
positively
correlated
infiltration
degree
CD8
T
cells
evaluated
six
algorithms.
it
found
sensitivities
drugs
Etoposide,
Imatinib,
Sorafenib,
Bosutinib
Sunitinib.
A
satisfactory
accuracy
survival
patients.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: April 25, 2025
AbstractBackground:
Glycolysis
and
lactylation
activity
significantly
impact
the
pathogenesis
of
Pulmonary
Arterial
Hypertension
(PAH);
however,
studies
exploring
their
heterogeneity
potential
correlation
at
single-cell
level
are
still
lacking.
Identifying
feature
genes
that
commonly
regulated
by
both
glycolysis
could
enhance
our
understanding
PAH.
Methods:
We
employed
RNA
sequencing
(scRNA-seq)
to
investigate
across
various
cellular
tiers
following
PAH,
aiming
acquire
comprehensive
biological
insights
into
We
Utilized
AUCell,
Ucell,
singscore,
ssGSEA,
AddModuleScore
algorithms
identify
common
positive
negative
in
PAH
level.
Furthermore,
we
three
machine
learning
algorithms,
Boruta,
Random
Forest,
SVM-RFE
optimal
related
BulkRNA-seq
further
leveraged
CellChat
pseudotime
analysis
delve
regulatory
mechanisms
characteristic
genes.
used
qPCR
detect
expression
ACTR2,
CCDC88A,
MRC1
rat
model
pulmonary
hypertension.
Results:
For
first
time
level,
discovered
activities
exhibit
different
cell
layers
However,
show
remarkable
consistency,
being
highly
active
macrophages,
fibroblasts,
monocytes,
epithelial
cells,
while
displaying
lower
lymphatic
endothelial
cells.
This
indicates
a
between
these
two
pathways
Consequently,
defined
set
co-regulate
Using
identified
key
predictive
for
namely
MRC1.
verify
excessive
Conclusions:
Following
might
simultaneously
upregulating
macrophages
monocytes
contribute
progression.
Clinical
trial
Not
applicable.
Frontiers in Bioscience-Landmark,
Journal Year:
2025,
Volume and Issue:
30(4)
Published: April 21, 2025
Background:
Hepatocellular
carcinoma
(HCC)
is
one
of
the
leading
causes
cancer
death
worldwide.
The
hypoxic
microenvironment
in
HCC
enhances
glycolysis
and
co-directed
lactate
accumulation,
which
leads
to
increased
lactylation.
However,
exact
biological
pattern
remains
be
elucidated.
Therefore,
we
sought
identify
hypoxia-glycolysis-lactylation
(HGL)
prognosis-related
signatures
validate
this
vitro.
Methods:
Transcriptomic
data
patients
with
were
collected
from
Cancer
Genome
Atlas
(TCGA),
International
Consortium
(ICGC),
Gene
Expression
Omnibus
(GEO)
databases.
Differentially
expressed
HGL
genes
between
normal
tissues
obtained
by
DEseq2.
consensus
clustering
algorithm
was
employed
stratify
into
two
distinct
clusters.
Subsequently,
single
sample
Set
Enrichment
Analysis
(ssGSEA),
Tumor
Immune
Estimation
Resource
(TIMER)
Dysfunction
Exclusion
(TIDE)
algorithms
utilized
assess
immune
infiltration
evasion.
Least
Absolute
Shrinkage
Selection
Operator
(LASSO)
COX
regression
analysis
used
an
signature.
Based
on
spatial
transcriptome
histological
data,
analyzed
expression
these
explored
function
Homer
Scaffold
Protein
1
(HOMER1)
cells.
Results:
We
identified
72
differentially
Cluster2,
better
survival
(p
<
0.001),
significantly
enriched
metabolic-related
pathways.
signature
exhibited
great
predictive
efficacy
for
TCGA,
ICGC,
GSE148355
databases
(3-year
area
under
curve
(AUC)
=
0.822,
0.738,
0.707,
respectively).
elevated
HOMER1
revealed
combination
data.
Knocking
down
inhibited
malignant
progression
Conclusions:
a
discovered
gene,
HOMER1,
that
influences
potential
become
novel
therapeutic
target.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Oct. 22, 2024
Lactylation,
a
novel
discovered
posttranslational
modification,
is
vital
component
of
lactate
function
and
prevalent
in
wide
range
cells,
interacting
with
both
histone
non-histone
proteins.
Recent
studies
have
confirmed
that
lactylation
as
new
contributor
to
epigenetic
landscape
involved
multiple
pathological
processes.
Accumulating
evidence
reveals
exists
different
pathophysiological
states
leads
inflammation
cancer;
however,
few
mechanisms
been
elaborated.
This
review
summarizes
the
biological
processes
roles
cancer,
well
discusses
relevant
potential
therapeutic
targets,
aiming
provide
insights
for
targeted
cancer
therapy.
Oncology Reports,
Journal Year:
2024,
Volume and Issue:
53(1)
Published: Nov. 8, 2024
Gastrointestinal
(GI)
cancers,
which
have
notable
incidence
and
mortality,
are
impacted
by
metabolic
reprogramming,
especially
the
increased
production
accumulation
of
lactate.
Lactylation,
a
post‑translational
modification
driven
lactate,
is
crucial
regulator
gene
expression
cellular
function
in
GI
cancer.
The
present
review
aimed
to
examine
advancements
understanding
lactate
lactylation
mechanisms
production,
its
influence
on
tumor
microenvironment
clinical
implications
levels
as
potential
biomarkers
were
explored.
Furthermore,
was
investigated,
including
biochemical
foundation,
primary
targets
functional
outcomes.
underscored
therapeutic
strategies
targeting
metabolism
lactylation.
Challenges
future
directions
emphasize
innovative
cancer
improve