Pharmaceutics,
Год журнала:
2025,
Номер
17(5), С. 555 - 555
Опубликована: Апрель 24, 2025
Background:
Advancements
in
pharmacogenomics,
artificial
intelligence
(AI),
and
CRISPR
gene-editing
technology
are
revolutionizing
precision
medicine
by
enabling
highly
individualized
therapeutic
strategies.
Artificial
intelligence-driven
computational
techniques
improve
biomarker
discovery
drug
optimization
while
pharmacogenomics
helps
to
identify
genetic
polymorphisms
affecting
metabolism,
efficacy,
toxicity.
Genetically
editing
based
on
presents
a
precise
method
for
changing
gene
expression
repairing
damaging
mutations.
This
review
explores
the
convergence
of
these
three
fields
enhance
improved
medicine.
Method:
A
methodical
study
current
literature
was
performed
effects
response
variability,
intelligence,
predictive
modeling
applications.
Results:
Driven
allows
clinicians
classify
patients
select
appropriate
medications
depending
their
DNA
profiles.
reduces
side
effect
risk
increases
efficacy.
Precision
modifications
made
feasible
therapy
outcomes
oncology,
metabolic
illnesses,
neurological
diseases,
other
fields.
The
integration
streamlines
genome-editing
applications,
lowers
off-target
effects,
specificity.
Notwithstanding
advances,
issues
including
biases,
moral
dilemmas,
legal
constraints
still
arise.
Conclusions:
synergy
alters
letting
customized
interventions.
Clinically
translating,
however,
hinges
resolving
data
privacy
concerns,
assuring
equitable
access,
strengthening
systems.
Future
research
should
focus
refining
technologies,
enhancing
AI-driven
developing
guidelines
applying
tools
going
forward.
Pharmaceuticals,
Год журнала:
2025,
Номер
18(1), С. 75 - 75
Опубликована: Янв. 10, 2025
Recent
developments
in
single-cell
multi-omics
technologies
have
provided
the
ability
to
identify
diverse
cell
types
and
decipher
key
components
of
tumor
microenvironment
(TME),
leading
important
advancements
toward
a
much
deeper
understanding
how
heterogeneity
contributes
cancer
progression
therapeutic
resistance.
These
are
able
integrate
data
from
molecular
genomic,
transcriptomic,
proteomics,
metabolomics
studies
cells
at
resolution
scale
that
give
rise
full
cellular
complexity
TME.
Understanding
complex
sometimes
reciprocal
relationships
among
cells,
CAFs,
immune
ECs
has
led
novel
insights
into
their
immense
functions,
which
can
consequences
on
behavior.
In-depth
uncovered
evasion
mechanisms,
including
exhaustion
T
metabolic
reprogramming
response
hypoxia
cells.
Single-cell
also
revealed
resistance
such
as
stromal
cell-secreted
factors
physical
barriers
extracellular
matrix.
Future
examining
specific
pathways
targeting
approaches
reduce
TME
will
likely
lead
better
outcomes
with
immunotherapies,
drug
delivery,
etc.,
for
treatments.
incorporate
data,
spatial
micro-environments,
translation
personalized
therapies.
This
review
emphasizes
provide
TME,
revealing
reprogramming,
influences.
aim
guide
development
targeted
therapies,
highlighting
role
diversity
shaping
behavior
treatment
outcomes.
Biomedicines,
Год журнала:
2025,
Номер
13(2), С. 422 - 422
Опубликована: Фев. 10, 2025
The
intricate
relationship
between
anticancer
drugs
and
the
gut
microbiome
influences
cancer
treatment
outcomes.
This
review
paper
focuses
on
role
of
integrity
in
enhancing
efficacy
safety
drug
therapy,
emphasizing
pharmacokinetic
interactions
microbiota.
It
explores
how
disruptions
to
composition,
or
dysbiosis,
can
alter
metabolism,
immune
responses,
side
effects.
By
examining
mechanisms
disruption
caused
by
drugs,
this
highlights
specific
case
studies
like
cyclophosphamide,
5-fluorouracil,
irinotecan,
their
impact
microbial
diversity
clinical
also
discusses
microbiome-targeted
strategies,
including
prebiotics,
probiotics,
postbiotics,
fecal
microbiota
transplantation
(FMT),
as
promising
interventions
enhance
treatment.
Furthermore,
potential
profiling
personalizing
therapy
integrating
these
into
practice
is
explored.
Finally,
proposes
future
research
directions,
developing
novel
biomarkers
a
deeper
comprehension
drug-microbiome
interactions,
respond
current
gaps
knowledge
improve
patient
outcomes
care.
Biomolecules,
Год журнала:
2025,
Номер
15(2), С. 270 - 270
Опубликована: Фев. 12, 2025
The
gut-brain-cancer
axis
represents
a
novel
and
intricate
connection
between
the
gut
microbiota,
neurobiology,
cancer
progression.
Recent
advances
have
accentuated
significant
role
of
microbiota
metabolites
in
modulating
systemic
processes
that
influence
both
brain
health
tumorigenesis.
This
paper
explores
emerging
concept
metabolite-mediated
modulation
within
connection,
focusing
on
key
such
as
short-chain
fatty
acids
(SCFAs),
tryptophan
derivatives,
secondary
bile
acids,
lipopolysaccharides
(LPS).
While
microbiota's
impact
immune
regulation,
neuroinflammation,
tumor
development
is
well
established,
gaps
remain
grasping
how
specific
contribute
to
neuro-cancer
interactions.
We
discuss
with
potential
implications
for
neurobiology
cancer,
indoles
polyamines,
which
yet
be
extensively
studied.
Furthermore,
we
review
preclinical
clinical
evidence
linking
dysbiosis,
altered
metabolite
profiles,
tumors,
showcasing
limitations
research
gaps,
particularly
human
longitudinal
studies.
Case
studies
investigating
microbiota-based
interventions,
including
dietary
changes,
fecal
transplantation,
probiotics,
demonstrate
promise
but
also
indicate
hurdles
translating
these
findings
therapies.
concludes
call
standardized
multi-omics
approaches
bi-directional
frameworks
integrating
microbiome,
neuroscience,
oncology
develop
personalized
therapeutic
strategies
patients.
Nutrients,
Год журнала:
2025,
Номер
17(5), С. 776 - 776
Опубликована: Фев. 23, 2025
Dyslipidemia,
characterized
by
abnormal
blood
lipid
levels,
is
a
major
public
health
concern
due
to
its
association
with
atherosclerotic
cardiovascular
disease
(ASCVD)
and
other
cardiometabolic
disorders.
In
this
context,
appropriate
nutrition
patterns
are
pivotal
as
they
represent
the
basic
approach
for
providing
wide
range
of
substantial
advantages.
The
best
evidence
dyslipidemia
management
offered
Mediterranean
Diet,
Plant-Based
High-Fiber
Diet
Anti-inflammatory
while
DASH
Ketogenic
have
also
been
shown
target
additional
pathological
features
like
hypertension
comorbidities.
bioactive
compounds
that
enriched
in
these
able
manage
include
monounsaturated
fatty
acids
such
ω-3,
polyphenols
oleuropein,
resveratrol,
flavonoids,
catechins,
carotenoids,
phytosterols
soluble
unsoluble
fibers.
Diets
rich
can
improve
profile
mitigating
oxidative
stress,
reducing
low-grade
chronic
inflammation,
modulating
macronutrient
absorption
mechanisms,
thereby
supporting
health.
Additionally,
lifestyle
interventions
regular
physical
activity,
weight
loss,
reduced
alcohol
consumption
smoking
cessation
further
ameliorate
metabolism
circulated
profile.
Furthermore,
emerging
insights
from
nutrigenomics
underscore
potential
proper
diet
address
genetic
factors
optimize
treatment
outcomes.
role
context
implications
discussed
review,
emphasizing
evidence-based
personalized
approaches.
Frontiers in Medicine,
Год журнала:
2025,
Номер
12
Опубликована: Фев. 26, 2025
Sarcoidosis
is
an
inflammatory
disease
characterized
by
the
formation
of
granulomas
in
various
organs,
leading
to
inflammation
and
potential
organ
dysfunction.
Symptoms
often
start
with
general
signs
like
fatigue,
fever,
weight
loss,
but
vary
depending
on
affected
organ.
Diagnosis
challenging
due
its
diverse
clinical
presentation
lack
a
definitive
test,
while
treatment
complicated
disease's
variable
course,
requiring
personalized
approach.
This
review
explores
role
genetic
environmental
factors
sarcoidosis
etiology,
examines
current
challenges
diagnosis
treatment,
discusses
how
understanding
etiology
informs
patient
management
future
strategies.
Abstract
Background
Genes
that
participate
in
the
absorption,
distribution,
metabolism,
excretion
(ADME)
processes
occupy
a
central
role
pharmacokinetics.
Meanwhile,
variability
clinical
outcomes
and
responses
to
treatment
is
notable
bladder
cancer
(BLCA).
Methods
Our
study
utilized
expansive
datasets
from
TCGA
GEO
explore
prognostic
factors
cancer.
Utilizing
both
univariate
Cox
regression
lasso
techniques,
we
identified
ADME
genes
critical
for
patient
outcomes.
our
study,
model
assessing
risk
was
constructed.
The
evaluation
of
this
model's
predictive
precision
conducted
using
Kaplan–Meier
survival
curves
assessments
based
on
ROC
curves.
Furthermore,
devised
nomogram,
offering
straightforward
visualization
crucial
indicators.
To
potential
mediating
differences
between
high
low
groups,
performed
comprehensive
analyses
including
Gene
Ontology
(GO)
Kyoto
Encyclopedia
Genomes
(KEGG)-based
enrichment
analyses,
immune
infiltration
variations,
somatic
mutation
landscapes,
pharmacological
sensitivity
response
assessment
etc.
Immediately
following
this,
selected
core
PPI
network
explored
as
well
modulation,
pathway
activation.
And
differential
expression
verified
by
immunohistochemistry
qRT-PCR.
Finally
pan-cancer
biomarkers.
Results
efforts
culminated
establishment
validated
17-gene
ADME-centered
prediction
model,
displaying
remarkable
accuracy
BLCA
prognosis.
Through
separate
cox
importance
model’s
score
forecasting
substantiated.
novel
nomogram
incorporating
variables
alongside
introduced.
Comprehensive
studies
established
strong
correlation
several
key
indicators:
patterns
cell
infiltration,
reactions
immunotherapy,
landscape
profiles
drug
sensitivity.
We
screened
gene
CYP2C8,
its
tumor
bioregulation
upregulated
found
it
can
serve
reliable
biomarker
pan-cancer.
Conclusion
formulated
research
stands
formidable
instrument
prognosis,
while
also
providing
insights
into
disease's
progression
mechanisms
guiding
decision-making
strategies.
Micromachines,
Год журнала:
2025,
Номер
16(4), С. 419 - 419
Опубликована: Март 31, 2025
The
rapid
evolution
of
micro-
and
nano-architectures
is
revolutionizing
biomedical
engineering,
particularly
in
the
fields
therapeutic
diagnostic
micromechanics.
This
review
explores
recent
innovations
nanostructured
materials
their
transformative
impact
on
healthcare
applications,
ranging
from
drug
delivery
tissue
engineering
to
biosensing
diagnostics.
Key
advances
fabrication
techniques,
such
as
lithography,
3D
printing,
self-assembly,
have
enabled
unprecedented
control
over
material
properties
functionalities
at
microscopic
scales.
These
engineered
architectures
offer
enhanced
precision
targeting
controlled
release
delivery,
foster
cellular
interactions
improve
sensitivity
specificity
devices.
We
examine
critical
design
parameters,
including
biocompatibility,
mechanical
resilience,
scalability,
which
influence
clinical
efficacy
long-term
stability.
also
highlights
translational
potential
current
limitations
bringing
these
laboratory
research
practical
applications.
By
providing
a
comprehensive
overview
trends,
challenges,
future
perspectives,
this
article
aims
inform
inspire
further
development
that
hold
promise
for
advancing
personalized
medicine.
Genomics
is
one
of
core
components
very
basic
biological
processes
transcription,
translation
and
peptide
molecule
synthesis,
collectively
known
as
the
‘central
dogma
life’.
This
basis
multitude
sciences
with
OMICS
suffix,
for
example,
transcriptomics,
proteomics,
metabolomics
others.
Almost
all
OMIC
have
direct
or
indirect
bearing
on
many
interrelated
relevant
to
integrated
molecular
pathways
systems
body
organs
functioning
tissues.
The
concept
multi-OMICS
medicine
now
supported
by
recurrent
outcomes
fundamental
applied
life
research.
common
purpose
deliver
healthcare
precisely
possible
targeted
at
specific
points
in
an
individual
patient
thus
satisfying
requirement
personalised
medicine.
There
growing
interest
evidence
integrate
traditional
ancient
like
Ayurveda.
review
provides
factual
information
context
evidence-based,
ethically
sound,
precision