Genome Medicine,
Journal Year:
2024,
Volume and Issue:
16(1)
Published: Jan. 18, 2024
Abstract
Spatial
multi-omic
studies
have
emerged
as
a
promising
approach
to
comprehensively
analyze
cells
in
tissues,
enabling
the
joint
analysis
of
multiple
data
modalities
like
transcriptome,
epigenome,
proteome,
and
metabolome
parallel
or
even
same
tissue
section.
This
review
focuses
on
recent
advancements
spatial
multi-omics
technologies,
including
novel
computational
approaches.
We
discuss
low-resolution
high-resolution
methods
which
can
resolve
up
10,000
individual
molecules
at
subcellular
level.
By
applying
integrating
these
techniques,
researchers
recently
gained
valuable
insights
into
molecular
circuits
mechanisms
govern
cell
biology
along
cardiovascular
disease
spectrum.
provide
an
overview
current
approaches,
with
focus
integration
datasets,
highlighting
strengths
weaknesses
various
pipelines.
These
tools
play
crucial
role
analyzing
interpreting
facilitating
discovery
new
findings,
enhancing
translational
research.
Despite
nontrivial
challenges,
such
need
for
standardization
experimental
setups,
analysis,
improved
tools,
application
holds
tremendous
potential
revolutionizing
our
understanding
human
processes
identification
biomarkers
therapeutic
targets.
Exciting
opportunities
lie
ahead
field
will
likely
contribute
advancement
personalized
medicine
diseases.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: March 20, 2023
Metabolic
abnormalities
lead
to
the
dysfunction
of
metabolic
pathways
and
metabolite
accumulation
or
deficiency
which
is
well-recognized
hallmarks
diseases.
Metabolite
signatures
that
have
close
proximity
subject's
phenotypic
informative
dimension,
are
useful
for
predicting
diagnosis
prognosis
diseases
as
well
monitoring
treatments.
The
lack
early
biomarkers
could
poor
serious
outcomes.
Therefore,
noninvasive
methods
with
high
specificity
selectivity
desperately
needed.
Small
molecule
metabolites-based
metabolomics
has
become
a
specialized
tool
biomarker
pathway
analysis,
revealing
possible
mechanisms
human
various
deciphering
therapeutic
potentials.
It
help
identify
functional
related
variation
delineate
biochemical
changes
indicators
pathological
damage
prior
disease
development.
Recently,
scientists
established
large
number
profiles
reveal
underlying
networks
target
exploration
in
biomedicine.
This
review
summarized
analysis
on
potential
value
small-molecule
candidate
metabolites
clinical
events,
may
better
diagnosis,
prognosis,
drug
screening
treatment.
We
also
discuss
challenges
need
be
addressed
fuel
next
wave
breakthroughs.
Science,
Journal Year:
2022,
Volume and Issue:
376(6590)
Published: April 14, 2022
Human
cells
produce
thousands
of
lipids
that
change
during
cell
differentiation
and
can
vary
across
individual
the
same
type.
However,
we
are
only
starting
to
characterize
function
these
cell-to-cell
differences
in
lipid
composition.
Here,
measured
lipidomes
transcriptomes
human
dermal
fibroblasts
by
coupling
high-resolution
mass
spectrometry
imaging
with
single-cell
transcriptomics.
We
found
variations
specific
metabolic
pathways
contribute
establishment
states
involved
organization
skin
architecture.
Sphingolipid
composition
is
shown
define
fibroblast
subpopulations,
sphingolipid
rewiring
driving
cell-state
transitions.
Therefore,
heterogeneity
affects
determination
states,
adding
a
new
regulatory
component
self-organization
multicellular
systems.
Genome biology,
Journal Year:
2022,
Volume and Issue:
23(1)
Published: April 14, 2022
Abstract
The
advancement
of
highly
multiplexed
spatial
technologies
requires
scalable
methods
that
can
leverage
information.
We
present
MISTy,
a
flexible,
scalable,
and
explainable
machine
learning
framework
for
extracting
relationships
from
any
omics
data,
dozens
to
thousands
measured
markers.
MISTy
builds
multiple
views
focusing
on
different
or
functional
contexts
dissect
effects.
evaluated
in
silico
breast
cancer
datasets
by
imaging
mass
cytometry
transcriptomics.
estimated
structural
interactions
coming
demonstrated
how
relate
MISTy’s
results
clinical
features.
Nature Metabolism,
Journal Year:
2022,
Volume and Issue:
4(9), P. 1109 - 1118
Published: Aug. 25, 2022
Abstract
A
common
drawback
of
metabolic
analyses
complex
biological
samples
is
the
inability
to
consider
cell-to-cell
heterogeneity
in
context
an
organ
or
tissue.
To
overcome
this
limitation,
we
present
advanced
high-spatial-resolution
metabolomics
approach
using
matrix-assisted
laser
desorption/ionization
mass
spectrometry
imaging
(MALDI-MSI)
combined
with
isotope
tracing.
This
method
allows
mapping
cell-type-specific
dynamic
changes
central
carbon
metabolism
a
heterogeneous
tissue
architecture,
such
as
kidney.
Combined
multiplexed
immunofluorescence
staining,
can
detect
and
nutrient
partitioning
targeted
cell
types,
demonstrated
bilateral
renal
ischemia–reperfusion
injury
(bIRI)
experimental
model.
Our
enables
us
identify
region-specific
perturbations
associated
lesion
throughout
recovery,
including
unexpected
anomalies
cells
apparently
normal
phenotype
recovery
phase.
These
findings
may
be
relevant
understanding
homeostatic
capacity
kidney
microenvironment.
In
sum,
achieve
resolution
at
single-cell
level
situ
hence
interpret
dynamics
structure
neighboring
cells.
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: March 22, 2023
Abstract
Tumour
cells
have
exquisite
flexibility
in
reprogramming
their
metabolism
order
to
support
tumour
initiation,
progression,
metastasis
and
resistance
therapies.
These
reprogrammed
activities
include
a
complete
rewiring
of
the
bioenergetic,
biosynthetic
redox
status
sustain
increased
energetic
demand
cells.
Over
last
decades,
cancer
field
has
seen
an
explosion
new
biochemical
technologies
giving
more
tools
than
ever
before
navigate
this
complexity.
Within
cell
or
tissue,
metabolites
constitute
direct
signature
molecular
phenotype
thus
profiling
concrete
clinical
applications
oncology.
Metabolomics
fluxomics,
are
key
technological
approaches
that
mainly
revolutionized
enabling
researchers
both
qualitative
mechanistic
model
cancer.
Furthermore,
upgrade
from
bulk
single-cell
analysis
provided
unprecedented
opportunity
investigate
biology
at
cellular
resolution
allowing
depth
quantitative
complex
heterogenous
diseases.
More
recently,
advent
functional
genomic
screening
allowed
identification
pathways,
processes,
biomarkers
novel
therapeutic
targets
concert
with
other
allow
patient
stratification
treatment
regimens.
This
review
is
intended
be
guide
for
metabolism,
highlighting
current
emerging
technologies,
emphasizing
advantages,
disadvantages
potential
leading
development
innovative
anti-cancer