Pharmacological Research - Modern Chinese Medicine,
Год журнала:
2024,
Номер
10, С. 100347 - 100347
Опубликована: Янв. 2, 2024
Gastric
cancer
is
one
of
the
common
malignancies
worldwide,
and
drug
resistance
a
major
factor
contributing
to
difficulty
treatment
in
gastric
cancer.
Zuojinwan
(ZJW)
has
been
found
exhibit
certain
inhibitory
effect
on
tumor
cells.
However,
molecular
mechanisms
ZJW
reversing
are
still
unclear.
Human
cisplatin-resistant
cells
SGC-7901/DDP
BGC-823/DDP
were
divided
into
control
groups,
DDP
groups
(10
μg/mL),
2-DG
(5
mM)
(50
μg/mL)
combined
with
groups.
After
48
hours
culture,
cell
proliferation
inhibition
rate,
glucose
uptake
ATP,
lactate
production
detected.
Following
lentiviral
transfection
overexpress
GLUT1
HDAC1,
western
blot
analysis
was
employed
examine
expression
P53,
Ace-p53,
metabolism-related
proteins
such
as
GLUT1,
LDHA,
HK
II
The
combination
significantly
inhibits
glycolysis
cisplatin
resistant
Compared
group,
exhibited
higher
rate
(P<
0.01),
accompanied
by
reduction
HDAC1
P53
proteins.
can
enhance
cells,
attenuate
glycolysis,
reduce
chemotherapy
resistance.
Its
mechanism
may
be
associated
HDAC1/P53
axis
activity.
Current Genomics,
Год журнала:
2023,
Номер
24(3), С. 136 - 145
Опубликована: Май 1, 2023
Epigenetic
changes
play
an
important
role
in
the
pathophysiology
of
autoimmune
diseases
such
as
allergic
asthma,
multiple
sclerosis,
lung
diseases,
diabetes,
cystic
fibrosis,
atherosclerosis,
rheumatoid
arthritis,
and
COVID-19.
There
are
three
main
classes
epigenetic
alterations:
post-translational
modifications
histone
proteins,
control
by
non-coding
RNA
DNA
methylation.
Since
can
directly
affect
chromatin
structure
accessibility,
they
regulate
gene
expression
levels.
Abnormal
activity
deacetylases
(HDACs)
have
been
reported
immune
mediated
diseases.
Increased
acetylated
levels
lysine
residues
suggested
to
be
related
overexpression
inflammatory
genes.
This
review
focuses
on
effect
HDAC
non-histone
proteins
Furthermore,
we
discuss
potential
therapeutic
inhibitors
(HDACi)
used
these
Cancers,
Год журнала:
2022,
Номер
14(18), С. 4401 - 4401
Опубликована: Сен. 10, 2022
Cancer
is
a
major
health
burden
worldwide.
Although
the
plethora
of
molecular
targets
identified
in
last
decades
and
deriving
developed
treatments,
which
significantly
improved
patients'
outcome,
occurrence
resistance
to
therapies
remains
cause
relapse
mortality.
Thus,
efforts
identifying
new
markers
be
exploited
as
cancer
therapy
are
needed.
This
review
will
first
give
glance
on
diagnostic
therapeutic
significance
histone
deacetylase
(HDAC)
voltage
gated
ion
channels
(VGICs)
cancer.
Nevertheless,
HDAC
VGICs
have
also
been
reported
through
antiepileptic
drugs
(AEDs)
seem
exert
their
anticancer
activity.
should
claimed
great
advantage.
Indeed,
due
slowness
drug
approval
procedures,
attempt
turn
off-label
use
already
approved
medicines
would
highly
preferable.
Therefore,
an
updated
accurate
overview
both
preclinical
clinical
data
commonly
prescribed
AEDs
(mainly
valproic
acid,
lamotrigine,
carbamazepine,
phenytoin
gabapentin)
breast,
prostate,
brain
other
cancers
follow.
Finally,
at
emerging
administer
by
means
opportunely
designed
delivery
systems
(DDSs),
so
limit
toxicity
improve
bioavailability,
given.
Pharmacological Research - Modern Chinese Medicine,
Год журнала:
2024,
Номер
10, С. 100347 - 100347
Опубликована: Янв. 2, 2024
Gastric
cancer
is
one
of
the
common
malignancies
worldwide,
and
drug
resistance
a
major
factor
contributing
to
difficulty
treatment
in
gastric
cancer.
Zuojinwan
(ZJW)
has
been
found
exhibit
certain
inhibitory
effect
on
tumor
cells.
However,
molecular
mechanisms
ZJW
reversing
are
still
unclear.
Human
cisplatin-resistant
cells
SGC-7901/DDP
BGC-823/DDP
were
divided
into
control
groups,
DDP
groups
(10
μg/mL),
2-DG
(5
mM)
(50
μg/mL)
combined
with
groups.
After
48
hours
culture,
cell
proliferation
inhibition
rate,
glucose
uptake
ATP,
lactate
production
detected.
Following
lentiviral
transfection
overexpress
GLUT1
HDAC1,
western
blot
analysis
was
employed
examine
expression
P53,
Ace-p53,
metabolism-related
proteins
such
as
GLUT1,
LDHA,
HK
II
The
combination
significantly
inhibits
glycolysis
cisplatin
resistant
Compared
group,
exhibited
higher
rate
(P<
0.01),
accompanied
by
reduction
HDAC1
P53
proteins.
can
enhance
cells,
attenuate
glycolysis,
reduce
chemotherapy
resistance.
Its
mechanism
may
be
associated
HDAC1/P53
axis
activity.