Exploring treatment options in cancer: Tumor treatment strategies
Signal Transduction and Targeted Therapy,
Год журнала:
2024,
Номер
9(1)
Опубликована: Июль 17, 2024
Traditional
therapeutic
approaches
such
as
chemotherapy
and
radiation
therapy
have
burdened
cancer
patients
with
onerous
physical
psychological
challenges.
Encouragingly,
the
landscape
of
tumor
treatment
has
undergone
a
comprehensive
remarkable
transformation.
Emerging
fervently
pursued
modalities
are
small
molecule
targeted
agents,
antibody-drug
conjugates
(ADCs),
cell-based
therapies,
gene
therapy.
These
cutting-edge
not
only
afford
personalized
precise
targeting,
but
also
provide
enhanced
comfort
potential
to
impede
disease
progression.
Nonetheless,
it
is
acknowledged
that
these
strategies
still
harbour
untapped
for
further
advancement.
Gaining
understanding
merits
limitations
holds
promise
offering
novel
perspectives
clinical
practice
foundational
research
endeavours.
In
this
review,
we
discussed
different
modalities,
including
drugs,
peptide
antibody
cell
therapy,
It
will
detailed
explanation
each
method,
addressing
their
status
development,
challenges,
solutions.
The
aim
assist
clinicians
researchers
in
gaining
deeper
diverse
options,
enabling
them
carry
out
effective
advance
more
efficiently.
Язык: Английский
Aspalathin-Rich Unfermented Aspalathus linearsis Extract Mitigates Vascular Endothelial Inflammation by Inhibiting the TNF-α/Hexokinase 2/NF-κB Signaling Pathway
Journal of Agriculture and Food Research,
Год журнала:
2025,
Номер
unknown, С. 101882 - 101882
Опубликована: Апрель 1, 2025
Язык: Английский
Immunometabolic reprogramming of macrophages with inhalable CRISPR/Cas9 nanotherapeutics for acute lung injury intervention
Wanling Huang,
Gaohong Fu,
Yangeng Wang
и другие.
Acta Biomaterialia,
Год журнала:
2024,
Номер
181, С. 308 - 316
Опубликована: Апрель 1, 2024
Язык: Английский
High-intensity interval training and medium-intensity continuous training may affect cognitive function through regulation of intestinal microbial composition and its metabolite LPS by the gut-brain axis
Mei Peng,
Ruihan Zou,
Sisi Yao
и другие.
Life Sciences,
Год журнала:
2024,
Номер
352, С. 122871 - 122871
Опубликована: Июнь 25, 2024
Язык: Английский
The impact of glycolysis on ischemic stroke: from molecular mechanisms to clinical applications
Frontiers in Neurology,
Год журнала:
2025,
Номер
16
Опубликована: Янв. 24, 2025
Ischemic
stroke
(IS),
a
leading
cause
of
disability
and
mortality
worldwide,
remains
significant
challenge
due
to
its
complex
pathogenesis.
Glycolysis,
central
metabolic
pathway,
plays
critical
role
in
bridging
the
gap
between
dysfunction
neurological
impairment.
During
ischemic
conditions,
glycolysis
replaces
oxidative
phosphorylation
as
primary
energy
source
for
brain
tissue.
However,
ischemia–reperfusion
state,
neuronal
cells
show
particular
reliance
on
aerobic
glycolysis.
Immune
cells,
such
monocytes,
also
contribute
atheromatous
plaque
formation
thrombi
through
increased
Given
glycolysis’s
involvement
various
pathological
stages
IS,
it
offers
potential
improved
diagnosis,
treatment,
prevention.
This
review
comprehensively
explores
different
phases
addresses
existing
controversies,
discusses
diagnostic
therapeutic
applications.
By
elucidating
intricate
relationship
this
aims
provide
novel
insights
future
research
clinical
advancements.
Язык: Английский
Antibiotic-derived approaches in cancer therapy: effectiveness of ikarugamycin in hexokinase-2 inhibition, tissue factor modulation, and metabolic regulation in breast cancer
Anti-Cancer Drugs,
Год журнала:
2025,
Номер
unknown
Опубликована: Янв. 29, 2025
We
aimed
to
explore
the
role
of
ikarugamycin
(IKA)
in
breast
cancer,
its
connection
with
hexokinase-2
(HK-2)
repression,
and
tissue
factor
(TF).
This
study
sought
extend
HK-2
as
a
TF
activator
comprehensive
analysis
these
interactions
from
enzyme,
gene,
protein
levels.
The
investigation
was
performed
MDA-MB-231
MCF-7
cancer
lines.
oxidative
stress
index
(OSI),
lactate
production,
HK
activity
were
assessed
using
colorimetric
assays.
Western
blot
quantitative
PCR
analyses
determine
expressions.
Prothrombin
time
Tests
additionally
effect
IKA
therapy
on
activation.
Three
over
four
significantly
downregulated
genes
identified
after
specific
IKA's
cell
In
treatment
group,
production
markedly
reduced
(P
<
0.05)
hexokinase
found
be
all
groups
0.05,
<0.01).
Paclitaxel
cytotoxicity
independently
causes
lower
OSI
IKA-treated
compared
controls
even
though
is
elevated
control.
Molecular
results
demonstrated
expressions
at
level
P
0.01).
Partial
thromboplastin
also
showed
that
cells
had
longer
activation
duration.
A
potential
indirect
association
inhibition
regulation
put
forward
this
by
presenting
bioactivation
protein,
enzyme
Язык: Английский
Cirsium japonicum leaf extract attenuated lipopolysaccharide-induced acute respiratory distress syndrome in mice via suppression of the NLRP3 and HIF1α pathways
Phytomedicine,
Год журнала:
2025,
Номер
140, С. 156601 - 156601
Опубликована: Март 2, 2025
Язык: Английский
Transcriptional and neuroprotective effects of hexokinase-2 inhibitors administered after stroke
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2025,
Номер
unknown
Опубликована: Апрель 17, 2025
ABSTRACT
The
inflammatory
response
induced
by
stroke
can
exacerbate
injury
to
peri-infarct
tissue.
Microglia
and
other
immune
cells
that
mediate
this
require
increased
glycolytic
flux
during
pro-inflammatory
activation.
These
cells,
unlike
neurons
most
cell
types,
utilize
hexokinase-2
(HK2)
rather
than
hexokinase-1
for
glycolysis,
such
HK2
inhibitors
may
selectively
target
them
suppress
post-ischemic
inflammation.
Here
we
compared
the
effects
of
non-selective
hexokinase
inhibitor
2-deoxyglucose
HK2-selective
lonidamine
3-bromopyruvate
on
secondary
after
stroke.
A
spatial
transcriptomic
assessment
was
performed
in
parallel
compare
microglial
gene
expression
microglia
-
neuron
interactions
screen
off-target
effects.
Each
suppressed
upregulation
attenuated
stress
functional
pathways
neighboring
neurons,
but
had
minimal
effect
neuronal
uninjured
cortex.
were
more
effective
suppressing
morphological
changes,
oxidative
stress,
neurite
loss.
administered
produced
long-term
improvements
outcome.
Selective
thus
provide
a
clinically
applicable
means
activation
thereby
improve
outcomes
without
endangering
energy
metabolism.
Язык: Английский
Methylglyoxal is an antibacterial effector produced by macrophages during infection
bioRxiv (Cold Spring Harbor Laboratory),
Год журнала:
2024,
Номер
unknown
Опубликована: Ноя. 3, 2024
Abstract
Infected
macrophages
transition
into
aerobic
glycolysis,
a
metabolic
program
crucial
for
control
of
bacterial
infection.
However,
antimicrobial
mechanisms
supported
by
glycolysis
are
unclear.
Methylglyoxal
is
highly
toxic
aldehyde
that
modifies
proteins
and
DNA
produced
as
side-product
glycolysis.
Here
we
show
despite
the
toxicity
this
aldehyde,
infected
generate
high
levels
methylglyoxal
during
while
downregulating
detoxification
system.
We
use
targeted
mutations
in
mice
to
modulate
generation
reducing
production
host
promotes
survival
Listeria
monocytogenes
Mycobacterium
tuberculosis
,
whereas
increasing
improves
Furthermore,
bacteria
unable
detoxify
avirulent
experience
up
1000-fold
greater
genomic
mutation
frequency
Taken
together,
these
results
suggest
an
innate
immune
effector
defends
against
pathogens.
Язык: Английский
Baicalein suppresses inflammation and attenuates acute lung injury by inhibiting glycolysis via HIF‑1α signaling
Molecular Medicine Reports,
Год журнала:
2024,
Номер
31(1)
Опубликована: Ноя. 5, 2024
Baicalein,
a
flavonoid
monomer
compound
isolated
from
the
dried
root
of
traditional
Chinese
herb
Scutellaria
baicalensis,
has
several
pharmacological
activities,
such
as
anti‑inflammatory,
anti‑angiogenic,
antitumor,
antimicrobial
and
antiviral
properties.
Acute
lung
injury
(ALI)
is
characterized
by
alveolar
epithelium
capillary
endothelium,
which
results
in
decreased
volume,
compliance,
ventilation/perfusion
mismatch,
intrapulmonary
edema,
edema
even
acute
hypoxemic
respiratory
failure.
The
present
study
aimed
to
investigate
effects
baicalein
on
inflammation.
Bioinformatics
analysis
using
network
pharmacology
predicted
that
hypoxia
inducible
factor‑1α
(HIF‑1α)
glycolysis
signaling
pathways
were
involved
mechanism
underlying
therapeutic
baicalein.
Further
in
vitro
vivo
experiments,
immunohistochemistry,
immunofluorescence
PCR,
verified
could
inhibit
HIF‑1α
signaling,
thus
suppressing
glycolysis,
improving
inflammatory
responses
ALI.
Taken
together,
suggested
anti‑inflammatory
treating
ALI
associated
with
its
ability
suppress
via
pathway.
Язык: Английский