The
morbidity
and
mortality
rates
of
prostate
cancer
(PCa)
are
high
among
elderly
men
worldwide.
Several
factors,
such
as
heredity,
obesity,
environment
associated
with
the
occurrence
PCa.
Cigarette
smoking,
which
is
also
an
important
factor
in
development
PCa,
can
lead
to
genetic
alterations
consequently
promote
PCa
development.
However,
smoking-induced
unclear.
This
study
aimed
identify
potential
smoking-related
genes
differentially
expressed
(DEGs)
were
identified
using
Gene
Expression
Omnibus
(GEO)
included
lots
datasets.
DEGs
subjected
protein–protein
interaction
(PPI)
network
analysis
hub
genes.
pathways
these
enriched
identified.
Cancer
Genome
Atlas
(TCGA)
dataset
was
used
examine
expression
samples
estimate
their
value
predicting
tumor
progression
prognosis.
In
total,
110
got
from
GSE68135
microarray
data
patients
smoking
or
not
14
key
PPI
network.
following
seven
altered
TCGA
patients:
EWSR1,
SRSF6,
COL6A3,
FBLN1,
DCN,
CYP2J2,
PLA2G2A.
CYP2J2
influenced
progression.
Additionally,
EWSR1
disease-free
survival.
logistic
regression
model,
exhibited
highest
risk
scores,
gene
for
We
found
one
genes:
truly
upregulated
clinical
cells
invasion
proliferation.
function
involved
Theranostics,
Год журнала:
2024,
Номер
14(7), С. 2946 - 2968
Опубликована: Янв. 1, 2024
Recent
advancements
in
modern
science
have
provided
robust
tools
for
drug
discovery.
The
rapid
development
of
transcriptome
sequencing
technologies
has
given
rise
to
single-cell
transcriptomics
and
single-nucleus
transcriptomics,
increasing
the
accuracy
accelerating
discovery
process.
With
evolution
spatial
(ST)
technology
emerged
as
a
derivative
approach.
Spatial
hot
topic
field
omics
research
recent
years;
it
not
only
provides
information
on
gene
expression
levels
but
also
offers
expression.
This
shown
tremendous
potential
disease
understanding
In
this
article,
we
introduce
analytical
strategies
review
its
applications
novel
target
mechanism
unravelling.
Moreover,
discuss
current
challenges
issues
that
need
be
addressed.
conclusion,
new
perspective
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(6), С. 3274 - 3274
Опубликована: Март 14, 2024
Throughout
history,
natural
products
have
played
a
significant
role
in
wound
healing.
Fibroblasts,
acting
as
primary
cellular
mediators
skin
healing,
exhibit
behavioral
responses
to
compounds
that
can
enhance
the
healing
process.
Identifying
bioactive
and
understanding
their
impact
on
fibroblast
behavior
offers
crucial
translational
opportunities
realm
of
Modern
scientific
techniques
enabled
detailed
how
naturally
derived
modulate
by
influencing
behavior.
Specific
known
for
properties
been
identified.
Engineered
biomimetic
replicating
microenvironment
are
designed
facilitate
normal
Advanced
delivery
methods
operating
at
micro-
nano-scales
developed
effectively
deliver
these
novel
through
stratum
corneum.
This
review
provides
comprehensive
summary
efficacy
promoting
regeneration
repair.
Additionally,
it
explores
engineering,
where
researchers
draw
inspiration
from
nature
create
materials
devices
mimicking
physiological
cues
effective
The
concludes
describing
mechanisms
aimed
enhancing
bioavailability
compounds.
Innovative
future
strategies
involve
exploring
fibroblast-influencing
pathways,
responsive
biomaterials,
smart
dressings
with
real-time
monitoring,
applications
stem
cells.
However,
translating
findings
clinical
settings
faces
challenges
such
limited
validation
biomaterials
large
animal
models
logistical
obstacles
industrial
production.
integration
ancient
remedies
modern
approaches
holds
promise
achieving
scar-free
Cancers,
Год журнала:
2024,
Номер
16(10), С. 1794 - 1794
Опубликована: Май 8, 2024
Angiogenesis
plays
a
pivotal
role
in
tumor
progression,
particularly
melanoma,
the
deadliest
form
of
skin
cancer.
This
review
synthesizes
current
knowledge
on
intricate
interplay
between
angiogenesis
and
microenvironment
(TME)
melanoma
progression.
Pro-angiogenic
factors,
including
VEGF,
PlGF,
FGF-2,
IL-8,
Ang,
TGF-β,
PDGF,
integrins,
MMPs,
PAF,
modulate
contribute
to
metastasis.
Additionally,
cells
within
TME,
such
as
cancer-associated
fibroblasts,
mast
cells,
melanoma-associated
macrophages,
influence
Anti-angiogenic
therapies,
while
showing
promise,
face
challenges
drug
resistance
tumor-induced
activation
alternative
angiogenic
pathways.
Rational
combinations
anti-angiogenic
agents
immunotherapies
are
being
explored
overcome
resistance.
Biomarker
identification
for
treatment
response
remains
crucial
personalized
therapies.
highlights
complexity
underscores
need
innovative
therapeutic
approaches
tailored
dynamic
TME.
Cancer Cell International,
Год журнала:
2024,
Номер
24(1)
Опубликована: Окт. 7, 2024
The
extracellular
matrix
(ECM)
is
a
complex,
dynamic
network
of
multiple
macromolecules
that
serve
as
crucial
structural
and
physical
scaffold
for
neighboring
cells.
In
the
tumor
microenvironment
(TME),
ECM
proteins
play
significant
role
in
mediating
cellular
communication
between
cancer-associated
fibroblasts
(CAFs)
tumor-associated
macrophages
(TAMs).
Revealing
modification
TME
necessitates
intricate
signaling
cascades
transpire
among
diverse
cell
populations
proteins.
advent
single-cell
sequencing
has
enabled
identification
refinement
specific
subpopulations,
which
substantially
enhanced
our
comprehension
milieu
given
us
high-resolution
perspective
on
diversity
However,
it
essential
to
integrate
data
establish
coherent
framework.
this
regard,
we
present
comprehensive
review
relationships
ECM,
TAMs,
CAFs.
This
encompasses
insights
into
released
by
TAMs
CAFs,
integration
TAM-ECM-CAF
axis,
potential
applications
limitations
targeted
therapies
serves
reliable
resource
focused
therapeutic
strategies
while
highlighting
intermediates
TME.
Cancers,
Год журнала:
2024,
Номер
16(5), С. 913 - 913
Опубликована: Фев. 23, 2024
Melanoma
progression
is
a
multistep
evolution
from
common
melanocytic
nevus
through
radial
superficial
growth
phase,
the
invasive
vertical
phase
finally
leading
to
metastatic
dissemination
into
distant
organs.
aggressiveness
largely
depends
on
propensity
metastasize,
which
means
capacity
escape
physiological
microenvironment
since
tissue
damage
due
primary
melanoma
lesions
generally
modest.
Physiologically,
epidermal
melanocytes
are
attached
basement
membrane,
and
their
adhesion/migration
under
control
of
surrounding
keratinocytes.
Thus,
compartment
represents
first
responsible
for
spread.
This
complex
process
involves
cell-cell
contact
broad
range
secreted
bioactive
molecules.
Invasion,
or
at
beginning
microinvasion,
implies
breakdown
dermo-epidermal
membrane
followed
by
migration
neoplastic
cells
in
papillary
dermis.
Correspondingly,
several
experimental
evidences
documented
structural
functional
rearrangement
entire
neoplasm
that
some
way
reflects
atypia
tumor
cells.
Lastly,
must
support
proliferation
survival
outside
normal
epidermal-melanin
units.
task
presumably
mostly
delegated
fibroblasts
ultimately
self-autonomous
review
will
discuss
remodeling
occurs
epidermis
during
formation
as
well
skin
changes
occur
independently
hyperproliferation
having
possible
pro-tumoral
features.
International Journal of Molecular Sciences,
Год журнала:
2024,
Номер
25(9), С. 5023 - 5023
Опубликована: Май 4, 2024
Melanoma
is
the
most
severe
and
fatal
form
of
skin
cancer,
resulting
from
multiple
gene
mutations
with
high
intra-tumor
inter-tumor
molecular
heterogeneity.
Treatment
options
for
patients
whose
disease
has
progressed
beyond
ability
surgical
resection
rely
on
currently
accepted
standard
therapies,
notably
immune
checkpoint
inhibitors
targeted
therapies.
Acquired
resistance
to
these
therapies
treatment-associated
toxicity
necessitate
exploring
novel
strategies,
especially
those
that
can
be
personalized
specific
and/or
populations.
Here,
we
review
current
landscape
progress
explore
what
oncology
techniques
may
entail
in
scope
melanoma.
Our
purpose
provide
an
up-to-date
summary
tools
at
our
disposal
work
circumvent
common
barriers
faced
when
battling
Pigment Cell & Melanoma Research,
Год журнала:
2025,
Номер
38(2)
Опубликована: Фев. 26, 2025
ABSTRACT
Skin
cutaneous
melanoma
(SKCM)
is
a
lethal
skin
cancer
with
poor
prognosis
and
limited
response
to
immunotherapy.
Cancer‐associated
fibroblasts
(CAFs)
are
key
contributors
tumor
progression,
therapy
resistance,
immunosuppression.
In
this
study,
mRNA
sequencing
clinical
data
from
SKCM
samples
were
obtained
The
Cancer
Genome
Atlas
(TCGA)
Gene
Expression
Omnibus
(GEO)
databases
evaluate
the
prognostic
significance,
therapeutic
implications,
potential
for
enhancing
immunotherapy
through
targeting
CAFs
in
SKCM.
A
CAF‐related
risk
model
comprising
nine
genes
was
developed,
revealing
that
patients
classified
as
low‐risk
exhibited
superior
survival
outcomes
increased
sensitivity
Spearman
correlation
analysis
identified
significant
associations
between
score
40
drugs,
well
resistance
17
drugs.
Additionally,
categorized
into
three
distinct
subgroups
SKCM,
antigen‐presenting
(apCAFs)
notably
suppressing
infiltration
of
anti‐tumor
immune
cells
strongly
correlating
prognosis.
summary,
offers
robust
tool
capable
predicting
both
sensitivity.
Moreover,
pivotal
role
apCAFs
within
microenvironment
suggests
these
may
enhance
efficacy
A
knowledge
graph
can
effectively
showcase
the
essential
characteristics
of
data
and
is
increasingly
emerging
as
a
significant
means
integrating
information
in
field
artificial
intelligence.
Coronary
artery
plaque
represents
etiology
cardiovascular
events,
posing
diagnostic
challenge
for
clinicians
who
are
confronted
with
multitude
nonspecific
symptoms.
To
visualize
hierarchical
relationship
network
molecular
mechanisms
underlying
properties
symptom
phenotypes,
patient
symptomatology
was
extracted
from
electronic
health
record
real-world
clinical
settings.
Phenotypic
networks
were
constructed
utilizing
protein‒protein
interaction
networks.
Machine
learning
techniques,
including
convolutional
neural
networks,
Dijkstra's
algorithm,
gene
ontology
semantic
similarity,
employed
to
quantify
biological
features
within
network.
The
resulting
then
utilized
train
K-nearest
neighbor
model,
yielding
23
symptoms,
41
association
rules,
61
hub
genes
across
three
types
plaques
studied,
achieving
an
area
under
curve
92.5%.
Weighted
correlation
analysis
pathway
enrichment
subsequently
identify
lipid
status-related
inflammation-associated
pathways
that
could
help
explain
differences
properties.
confirm
validity
we
conducted
coexpression
evaluate
their
potential
value.
Additionally,
investigated
immune
cell
infiltration,
examined
correlations
between
cells,
validated
reliability
identified
pathways.
By
information,
this
biomedical
model
elucidated
collude
diseases,
molecules.
Current Pharmaceutical Design,
Год журнала:
2024,
Номер
30(10), С. 727 - 741
Опубликована: Март 1, 2024
Abstract:
This
review
investigates
the
revolutionary
application
of
cell
membrane-coated
nanoparticles
(CMNPs)
as
a
promising
avenue
for
cancer
therapy
within
embryonic
landscape
nanotechnology.
Nanoparticles,
pivotal
in
treatment,
are
systematically
examined
their
diverse
physicochemical
structures,
categorized
organic
(lipid-based,
protein-based,
and
polymer-assisted)
inorganic
(carbon-based
metal)
varieties.
A
significant
focus
is
placed
on
CMNPs,
which
serve
an
innovative
drug
delivery
vehicle,
overcoming
limitations
associated
with
conventional
nanoparticle
therapies.
manuscript
accurately
explores
advantages
challenges
various
membranes,
including
those
derived
from
cells,
red
blood
platelets,
stem
white
cells.
Importance
roles
enhancing
precision,
immune
system
circumvention,
targeted
recognition.
Detailed
insights
into
crafting
CMNPs
provided,
elucidating
membrane
extraction
fusion
techniques,
such
sonication,
extrusion,
co-extrusion,
microfluidic
electroporation.
Maintaining
integrity
during
benefits
coating
techniques
augmenting
biocompatibility
underscored.
comprehensive
resource
consolidates
latest
advancements
delivery,
positioning
itself
at
forefront
nanotechnology
biomedicine
research.
Encapsulating
methodologies
like
electrospray,
chemical
conjugation,
this
showcases
expanding
toolbox
available
to
researchers
dynamic
field.
Focusing
unique
characteristics
multifaceted
applications
biomedical
research,
particularly
tumour
therapy.
It
provides
indepth
analysis
stability,
evasion
capabilities,
increased
payload
capacity,
retained
biological
functionality.
The
outlines
current
future
prospects
chemotherapy,
photothermal
photodynamic
therapy,
immunotherapy,
gene
therapeutic
methods.
concludes
by
highlighting
transformative
potential
reshaping
treatment.