Scientific Reports,
Год журнала:
2024,
Номер
14(1)
Опубликована: Март 10, 2024
Abstract
Globally,
breast
cancer
is
the
second
most
common
cause
of
cancer-related
deaths
among
women.
In
cancer,
microRNAs
(miRNAs)
are
essential
for
both
initiation
and
development
tumors.
It
has
been
suggested
that
tumor
suppressor
microRNA-561-3p
(miR-561-3p)
crucial
in
arresting
growth
cells.
Further
research
necessary
to
fully
understand
role
molecular
mechanism
miR-561
human
BC.
The
aim
this
study
was
investigate
inhibitory
effect
miR-561-3p
on
ZEB1
,
HIF1A
MYC
expression
as
oncogenes
have
impact
PD-L1
overexpression
cellular
processes
such
proliferation,
apoptosis,
cell
cycle
(BC)
lines.
genes
were
measured
BC
clinical
samples
lines
via
qRT-PCR.
luciferase
assay,
MTT,
Annexin-PI
staining,
experiments
used
assess
candidate
gene
expression,
progression.
Flow
cytometry
effects
suppression
line.
assay
showed
miRNA-561-3p
targets
3′-UTRs
significantly.
tissues,
qRT-PCR
results
demonstrated
downregulated
up-regulated.
shown
decreased
induced
apoptosis
arrest
through
downregulation
oncogenes.
Furthermore,
inhibition
by
reduced
at
mRNA
protein
levels.
Our
investigated
cells
first
time.
findings
may
help
clarify
regulation
point
miR
a
potential
biomarker
novel
therapeutic
target
immunotherapy.
Frontiers in Immunology,
Год журнала:
2020,
Номер
11
Опубликована: Окт. 21, 2020
Programmed
death-ligand
1
(PD-L1)
is
an
immune
checkpoint
inhibitor
that
binds
to
its
receptor
PD-1
expressed
by
T
cells
and
other
regulate
responses;
ultimately
preventing
exacerbated
activation
autoimmunity.
Many
tumours
exploit
this
mechanism
overexpressing
PD-L1
which
often
correlates
with
poor
prognosis.
Some
have
also
recently
been
shown
express
PD-1.
On
tumours,
binding
on
promotes
evasion
tumour
progression,
primarily
inhibition
of
cytotoxic
lymphocyte
effector
function.
PD-1/PD-L1-targeted
therapy
has
revolutionised
the
cancer
landscape
become
first-line
treatment
for
some
cancers,
due
their
ability
promote
durable
anti-tumour
responses
in
select
patients
advanced
cancers.
Despite
clinical
success,
be
unresponsive,
hyperprogressive
or
develop
resistance
therapy.
The
exact
mechanisms
are
still
unclear.
This
review
will
discuss
current
status
therapy,
new
emerging
tumour-intrinisic
roles
how
they
may
contribute
progression
immunotherapy
as
different
oncology
models.
Journal of Translational Medicine,
Год журнала:
2024,
Номер
22(1)
Опубликована: Янв. 3, 2024
Abstract
Breast
cancer
(BC)
is
a
multifaceted
disease
characterized
by
distinct
molecular
subtypes
and
varying
responses
to
treatment.
In
BC,
the
phosphatidylinositol
3-kinase
(PI3K)
pathway
has
emerged
as
crucial
contributor
development,
advancement,
resistance
This
review
article
explores
implications
of
PI3K
in
predictive,
preventive,
personalized
medicine
for
BC.
It
emphasizes
identification
predictive
biomarkers,
such
PIK3CA
mutations,
utility
profiling
guiding
treatment
decisions.
The
also
discusses
potential
targeting
preventive
strategies
customization
therapy
based
on
tumor
stage,
subtypes,
genetic
alterations.
Overcoming
inhibitors
exploring
combination
therapies
are
addressed
important
considerations.
While
this
field
holds
promise
improving
patient
outcomes,
further
research
clinical
trials
needed
validate
these
approaches
translate
them
into
practice.
Graphical
Antioxidants,
Год журнала:
2021,
Номер
10(3), С. 349 - 349
Опубликована: Фев. 26, 2021
Doxorubicin
(DOX)
is
extensively
applied
in
cancer
therapy
due
to
its
efficacy
suppressing
progression
and
inducing
apoptosis.
After
discovery,
this
chemotherapeutic
agent
has
been
frequently
used
for
therapy,
leading
chemoresistance.
Due
dose-dependent
toxicity,
high
concentrations
of
DOX
cannot
be
administered
patients.
Therefore,
experiments
have
directed
towards
revealing
underlying
mechanisms
responsible
resistance
ameliorating
adverse
effects.
Nuclear
factor
erythroid
2-related
2
(Nrf2)
signaling
activated
increase
levels
reactive
oxygen
species
(ROS)
cells
protect
them
against
oxidative
stress.
It
reported
that
Nrf2
activation
associated
with
drug
resistance.
In
exposed
DOX,
stimulation
protects
cell
death.
Various
upstream
mediators
regulate
Strategies,
both
pharmacological
genetic
interventions,
reversing
However,
induction
importance
alleviating
side
effects
DOX.
Pharmacological
agents
naturally
occurring
compounds
as
the
most
common
amelioration.
Furthermore,
networks
which
a
key
player
protection
revealed
are
discussed
current
review.
Biomedicine & Pharmacotherapy,
Год журнала:
2020,
Номер
133, С. 110986 - 110986
Опубликована: Ноя. 7, 2020
Phosphatase
and
tensin
homolog
(PTEN)
gene
encodes
a
tumor
suppressor
protein
which
is
altered
in
several
malignancies.
This
negative
regulator
of
the
PI3K/AKT
signaling.
Several
transcription
factors
regulate
expression
PTEN
positive
or
directions.
Moreover,
numerous
microRNAs
(miRNAs)
have
functional
interactions
with
inhibit
its
expression.
Suppression
can
attenuate
response
cancer
cells
to
chemotherapeutic
agents.
Based
on
critical
role
this
gene,
identification
regulators
has
practical
significance
particularly
prevention
management
cancer.
Meanwhile,
interaction
between
miRNAs
consequences
non-malignant
disorders
including
myocardial
infarction,
osteoporosis,
cerebral
ischemic
stroke,
recurrent
abortion.
In
present
review,
we
describe
regulation
activity
PTEN.
Biomolecules,
Год журнала:
2021,
Номер
11(2), С. 304 - 304
Опубликована: Фев. 18, 2021
MicroRNAs
(miRNAs)
are
well-known
regulators
of
biological
mechanisms
with
a
small
size
19-24
nucleotides
and
single-stranded
structure.
miRNA
dysregulation
occurs
in
cancer
progression.
miRNAs
can
function
as
tumor-suppressing
or
tumor-promoting
factors
via
regulating
molecular
pathways.
Breast
lung
cancers
two
malignant
thoracic
tumors
which
the
abnormal
expression
plays
significant
role
their
development.
Phosphatase
tensin
homolog
(PTEN)
is
tumor-suppressor
factor
that
capable
suppressing
growth,
viability,
metastasis
cells
downregulating
phosphatidylinositol
3-kinase
(PI3K)/protein
kinase
B
(Akt)
signaling.
PTEN
downregulation
breast
to
promote
PI3K/Akt
expression,
leading
uncontrolled
proliferation,
metastasis,
resistance
chemotherapy
radiotherapy.
upstream
mediators
dually
induce/inhibit
signaling
affecting
behavior
cells.
Furthermore,
long
non-coding
RNAs
circular
regulate
miRNA/PTEN
axis
It
seems
anti-tumor
compounds
such
baicalein,
propofol,
curcumin
induce
upregulation
by
These
topics
discussed
current
review
focus
on
Journal of Hematology & Oncology,
Год журнала:
2021,
Номер
14(1)
Опубликована: Окт. 15, 2021
Abstract
Altered
metabolic
patterns
in
tumor
cells
not
only
meet
their
own
growth
requirements
but
also
shape
an
immunosuppressive
microenvironment
through
multiple
mechanisms.
Noncoding
RNAs
constitute
approximately
60%
of
the
transcriptional
output
human
and
have
been
shown
to
regulate
numerous
cellular
processes
under
developmental
pathological
conditions.
Given
extensive
action
mechanisms
based
on
motif
recognition
patterns,
noncoding
may
serve
as
hinges
bridging
activity
immune
responses.
Indeed,
recent
studies
that
microRNAs,
long
circRNAs
are
widely
involved
rewiring,
cell
infiltration
function.
Hence,
we
summarized
existing
knowledge
role
remodeling
metabolism
microenvironment,
notably,
established
TIMELnc
manual,
which
is
a
free
public
manual
for
researchers
identify
pivotal
lncRNAs
simultaneously
correlated
with
bioinformatic
approach.
Blood Science,
Год журнала:
2023,
Номер
5(2), С. 77 - 91
Опубликована: Янв. 13, 2023
Programmed
death-ligand
1
(PD-L1),
expressed
on
the
surface
of
tumor
cells,
can
bind
to
programmed
cell
death-1
(PD-1)
T
cells.
The
interaction
PD-1
and
PD-L1
inhibit
T-cell
responses
by
decreasing
activity
accelerating
their
apoptosis.
Various
cancers
express
high
levels
exploit
PD-L1/PD-1
signaling
evade
immunity,
immunotherapies
targeting
PD-1/PD-L1
axis
have
been
shown
exert
remarkable
anti-tumor
effects;
however,
not
all
patients
benefit
from
these
therapies.
Therefore,
study
mechanisms
regulating
expression
are
imperative.
In
this
review,
we
explore
regulation
in
contexts
gene
transcription,
pathways,
histone
modification
remodeling,
microRNAs,
long
noncoding
RNAs,
post-translational
modification.
Current
developments
studies
agents
that
block
correlations
between
also
summarized.
Our
review
will
assist
understanding
discusses
implications
reported
findings
cancer
diagnosis
immunotherapy.