Биохимия,
Journal Year:
2023,
Volume and Issue:
88(7), P. 1191 - 1203
Published: Dec. 15, 2023
Aberrant
methylation
and
acetylation
of
histones
are
characteristic
changes
in
the
system
epigenetic
regulation
gene
expression
accompanying
process
malignant
transformation
cell.
Vorinostat
is
modulator
that
actively
used
clinical
oncology
practice.
The
antitumor
activity
vorinostat
considered
to
be
associated
with
only
inhibition
histone
deacetylases.
effects
this
drug
on
have
not
been
sufficiently
studied.
Using
HeLa
TI
test
system,
which
allows
evaluating
integral
effect
epigenetically
active
compounds
by
activating
reporter
GFP,
knockdown
genes
small
interfering
RNAs,
we
showed
inhibitory
directed
at
HDAC1,
but
also
EZH2,
SUV39H1,
SUV39H2,
SUV420H1.
Western
blotting,
ability
suppress
enzymes
SUV39H1/2,
SUV420H1
was
confirmed
and,
addition,
its
inhibit
SUV420H2
DOT1L
revealed.
data
obtained
expand
understanding
demonstrate
need
for
a
large-scale
analysis
relation
other
enzymes.
A
detailed
mechanism
action
will
contribute
more
adequate
use
treatment
tumors
an
aberrant
profile.
Experimental Hematology and Oncology,
Journal Year:
2023,
Volume and Issue:
12(1)
Published: June 2, 2023
Abstract
Hepatocellular
carcinoma
(HCC)
is
the
leading
cause
of
cancer-related
death.
The
accumulation
genetic
and
epigenetic
changes
closely
related
to
occurrence
development
HCC.
Enhancer
zeste
homolog
2
(EZH2,
a
histone
methyltransferase)
suggested
be
one
principal
factors
that
mediates
oncogenesis
by
acting
as
driver
alternation.
Recent
studies
show
EZH2
widely
involved
in
proliferation
metastasis
HCC
cells.
In
this
review,
functions
progression,
role
tumor
immunity
application
EZH2-related
inhibitors
therapy
are
summarized.
FEBS Journal,
Journal Year:
2024,
Volume and Issue:
unknown
Published: July 31, 2024
Transforming
growth
factor‐β
(TGF‐β)
plays
a
complex
role
in
lung
cancer
pathophysiology,
initially
acting
as
tumor
suppressor
by
inhibiting
early‐stage
growth.
However,
its
evolves
the
advanced
stages
of
disease,
where
it
contributes
to
progression
not
directly
promoting
cell
proliferation
but
enhancing
epithelial–mesenchymal
transition
(EMT)
and
creating
conducive
microenvironment.
While
EMT
is
typically
associated
with
enhanced
migratory
invasive
capabilities
rather
than
per
se
,
TGF‐β's
influence
on
this
process
facilitates
dynamics
metastasis.
Additionally,
TGF‐β
impacts
microenvironment
interacting
immune
cells,
influenced
genetic
epigenetic
changes
within
cells.
This
interaction
highlights
evasion
chemoresistance,
further
complicating
therapy.
review
provides
critical
overview
recent
findings
involvement
cancer,
contribution
modulation
response.
Despite
considerable
challenges
encountered
clinical
trials
development
new
treatments
targeting
pathway,
necessity
for
continued,
in‐depth
investigation
into
roles
TGF‐β.
A
deeper
comprehension
these
may
lead
novel,
targeted
therapies
cancer.
intricate
behavior
signaling
tumors
previous
challenges,
research
could
yield
innovative
treatment
strategies.
Frontiers in Cellular and Infection Microbiology,
Journal Year:
2024,
Volume and Issue:
14
Published: May 21, 2024
Mycobacterium
tuberculosis
(M.tb)
,
the
causative
agent
of
Tuberculosis,
is
an
intracellular
bacterium
well
known
for
its
ability
to
subvert
host
energy
and
metabolic
pathways
maintain
survival.
For
this
purpose,
bacteria
utilize
various
mechanisms
which
extracellular
vehicles
(EVs)
related
attracted
more
attention.
EVs
are
nanosized
particles
that
released
by
almost
all
cell
types
containing
active
biomolecules
from
origin
can
target
bioactive
in
recipient
cells
upon
uptake.
It
hypothesized
M.tb
dictates
processes
EV
biogenesis
pathways,
selectively
incorporating
molecules
into
direct
immune
responses
favor.
During
infection
with
Mtb
both
mycobacteria
release
EVs.
The
composition
these
varies
over
time,
influenced
physiological
nutritional
state
environment.
Additionally,
different
populations
contribute
differently
pathogenesis
disease
at
stages
illness
participating
a
complex
interplay
between
pathogens.
These
interactions
ultimately
influence
outcomes.
However,
precise
roles
pathogenicity
outcomes
remain
be
fully
elucidated.
In
review,
we
explored
properties
function
context
within
microenvironment
discussed
their
capacity
as
novel
therapeutic
strategy
combat
tuberculosis.
BMC Pulmonary Medicine,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: Feb. 14, 2024
Lung
adenocarcinoma
(LUAD)
has
high
morbidity
and
mortality.
Despite
substantial
advances
in
treatment,
the
prognosis
of
patients
with
LUAD
remains
unfavorable.
The
ceRNA
axis
been
reported
to
play
an
important
role
pathogenesis
LUAD.
In
addition,
cuproptosis
is
considered
factor
tumorigenesis.
expression
CBX2
associated
development
multiple
tumors,
including
However,
precise
molecular
mechanisms
through
which
cuproptosis-related
network
regulates
remain
unclear.
Biochemistry (Moscow),
Journal Year:
2023,
Volume and Issue:
88(7), P. 968 - 978
Published: July 1, 2023
Epigenetic
genome
regulation
during
malignant
cell
transformation
is
characterized
by
the
aberrant
methylation
and
acetylation
of
histones.
Vorinostat
(SAHA)
an
epigenetic
modulator
actively
used
in
clinical
oncology.
The
antitumor
activity
vorinostat
commonly
believed
to
be
associated
with
inhibition
histone
deacetylases,
while
impact
this
drug
on
has
been
poorly
studied.
Using
HeLa
TI
cells
as
a
test
system
allowing
evaluation
effect
epigenetically
active
compounds
from
expression
GFP
reporter
gene
knockdown
small
interfering
RNAs,
we
showed
that
not
only
suppressed
HDAC1,
but
also
reduced
EZH2,
SUV39H1,
SUV39H2,
SUV420H1.
ability
suppress
SUV39H1/2,
SUV420H1
was
confirmed
Western
blotting.
downregulated
SUV420H2
DOT1L
enzymes.
data
obtained
expand
our
understanding
effects
demonstrate
need
for
large-scale
analysis
its
toward
other
enzymes
involved
regulation.
Elucidation
mechanism
underlying
action
will
contribute
more
proper
use
treatment
tumors
profile.
International Journal of Biological Sciences,
Journal Year:
2023,
Volume and Issue:
19(15), P. 4834 - 4848
Published: Jan. 1, 2023
The
aberrant
expression
of
methylation
and
ncRNAs,
two
crucial
regulators
epigenetic
modifications,
has
been
widely
demonstrated
in
cancer.The
complex
interplay
between
them
is
essential
promoting
malignant
phenotype,
poor
prognosis,
drug
resistance
GI
tumors
(including
esophageal,
gastric,
colorectal,
liver,
pancreatic
cancers).Therefore,
we
summarize
the
interrelation
process
ncRNAs
modifications
tumors,
including
detailed
mechanism
enzyme
regulation
molecular
correlation
interactions
clinical
features
tumors.Finally,
discuss
potential
value
diagnosis
therapy.
Discovery Medicine,
Journal Year:
2024,
Volume and Issue:
36(184), P. 1041 - 1041
Published: Jan. 1, 2024
Hepatocellular
carcinoma
(HCC)
stands
out
as
one
of
the
most
prevalent
malignant
tumors
globally.
The
combination
all-trans-retinoic
acid
(ATRA)
with
FOLFOX
chemotherapy
has
shown
promise
in
enhancing
prognosis
HCC
patients.
ATRA,
serving
a
chemosensitizing
agent,
presents
novel
possibilities
for
therapeutic
applications.
Nevertheless,
responsiveness
cells
to
ATRA
varies.
epigenetic
modifier-GSK-126
is
currently
under
investigation
potential
antitumor
drug.
Our
aim
explore
molecular
mechanisms
underlying
diverse
sensitivity
patients
and
propose
new
regimen.
This
research
aims
lay
groundwork
personalized
medication
approaches
individuals
HCC.
medRxiv (Cold Spring Harbor Laboratory),
Journal Year:
2024,
Volume and Issue:
unknown
Published: April 22, 2024
Abstract
In
recent
years,
research
on
the
competing
endogenous
RNAs
(ceRNAs)
in
cancer
is
full
swing.
These
investigations
are
discovering
importance
of
critical
progression.
Enhancer
zeste
2
polycomb
repressive
complex
subunit
(
EZH2
)
one
these
that
has
been
identified
as
a
potential
therapeutic
target
many
types
cancer.
Up
to
now,
studies
have
conducted
elucidate
ceRNA
role
Due
EZH2’s
dual
an
oncogene
and
tumor
suppressor
cancer,
more
thorough
exploration
its
functions
may
enhance
clinical
approaches
treatment.
current
scoping
review,
we
searched
online
databases
including
PubMed,
Web
Science,
Scopus,
Embase,
Cochrane
Library,
Google
Scholar
identify
experimentally-validated
axes
human
cancers.
We
62
unique
consisting
30
microRNAs
(miRNAs),
31
long
non-coding
(lncRNAs),
9
messenger
(mRNAs),
14
circular
(circRNAs).
Notably,
SPRY4-IT1
-
miR-101-3p
XIST
were
recurrent
observed
multiple
types.
Among
most
frequent
miRNAs
miR-101-3p,
miR-144-3p,
miR-124-3p,
ceRNAs
,
SNHG6
HOXA11-AS
MALAT1
TUG1
emerged
competitors
for
miRNA
binding.
This
review
highlights
prevalence
diversity
-containing
suggesting
their
targets.
Future
should
delve
deeper
into
functional
significance
assess
applicability.