Abstract
Recently,
extracellular
vesicles
(EVs)
have
been
emphasized
in
regulating
the
hypoxic
tumor
microenvironment
of
breast
cancer
(BC),
where
tumor‐associated
fibroblasts
(TAFs)
play
a
significant
role.
In
this
study,
we
describe
possible
molecular
mechanisms
behind
pro‐tumoral
effects
EVs,
secreted
by
hypoxia
(HP)‐induced
TAFs,
on
BC
cell
growth,
metastasis,
and
chemoresistance.
These
are
based
long
noncoding
RNA
H19
(H19)
identified
microarray
analysis.
We
employed
an
silico
approach
to
identify
differentially
expressed
lncRNAs
that
were
associated
with
BC.
Subsequently,
explored
downstream
regulatory
mechanisms.
isolated
EVs
from
TAFs
exposed
HP,
these
denoted
as
HP‐TAF‐EVs
henceforth.
MTT,
transwell,
flow
cytometry,
TUNEL
assays
performed
assess
malignant
phenotypes
cells.
A
paclitaxel
(TAX)‐resistant
line
was
constructed,
xenograft
lung
metastasis
models
established
nude
mice
for
vivo
verification.
Our
observation
revealed
lncRNA
significantly
overexpressed,
whereas
miR‐497
notably
downregulated
HP
induced
activation
stimulated
secretion
EVs.
Coculture
cells
led
increase
TAX
resistance
latter.
upregulated
methylation
delivering
H19,
which
recruited
DNMT1,
thus
lowering
expression
miR‐497.
addition,
H19‐containing
hindered
expression,
enhancing
tumorigenesis
vivo.
study
presents
evidence
contribution
reduction
through
recruitment
turn
promotes
chemoresistance
Breast Cancer,
Год журнала:
2022,
Номер
unknown, С. 31 - 42
Опубликована: Июнь 22, 2022
Breast
cancer
is
a
genetically
and
clinically
heterogeneous
disease
with
multiple
subtypes.
The
classification
of
these
subtypes
has
evolved
over
the
years.
most
common
widely
accepted
breast
from
an
immunohistochemical
perspective,
based
on
expression
following
hormone
receptors:
estrogen
(ER),
progesterone
(PR)
human
epidermal
growth
factor
(HER2).
Accordingly,
four
are
recognized:
luminal
A,
B,
HER2-positive,
triple
negative.
With
recent
advances
in
research,
increased
molecular
understanding
cancer,
current
clinical
model
for
may
be
benefit
addition
several
markers
such
as
miRNAs
(let-7,
miR-155,
miR-150,
miR-153)
mutations
(p53,
BRCA
1
2
genes).
This
chapter
provides
overview
characteristics
cancer.
Frontiers in Immunology,
Год журнала:
2022,
Номер
13
Опубликована: Окт. 28, 2022
Tumor-infiltrating
lymphocytes
(TILs),
frontline
soldiers
of
the
adaptive
immune
system,
are
recruited
into
tumor
site
to
fight
against
tumors.
However,
their
small
number
and
reduced
activity
limit
ability
overcome
tumor.
Enhancement
TILs
tumors
has
been
interest
for
a
long
time.
A
lack
knowledge
about
microenvironment
(TME)
limited
success
in
primary
TIL
therapies.
Although
advent
engineered
T
cells
revolutionized
immunotherapy
methods
hematologic
cancers,
heterogeneity
solid
warrants
application
with
wide
range
specificity.
Recent
advances
understanding
TME,
exhaustion,
checkpoints
have
paved
way
therapy
regimens.
Nowadays,
regained
attention
as
safe
personalized
immunotherapy,
currently,
several
clinical
trials
evaluating
efficacy
patients
who
failed
conventional
immunotherapies.
Gaining
favorable
outcomes
following
metastatic
melanoma,
cervical
cancer,
ovarian
breast
cancer
raised
hope
refractory
tumors,
too.
Nevertheless,
procedures
face
challenges,
such
high
cost,
timely
expansion,
technical
challenges
selecting
activating
cells.
Herein,
we
reviewed
recent
discussed
perspectives.
International Journal of Biological Sciences,
Год журнала:
2022,
Номер
18(6), С. 2609 - 2626
Опубликована: Янв. 1, 2022
Breast
cancer
rises
as
the
most
commonly
diagnosed
in
2020.Among
women,
breast
ranks
first
both
incidence
rate
and
mortality.Treatment
resistance
developed
from
current
clinical
therapies
limits
efficacy
of
therapeutic
outcomes,
thus
new
treatment
approaches
are
urgently
needed.Chimeric
antigen
receptor
(CAR)
T
cell
therapy
is
a
type
immunotherapy
adoptive
transfer,
which
typically
uses
patients'
own
immune
cells
to
combat
cancer.CAR-T
armed
with
specific
antibodies
recognize
antigens
self-tumor
eliciting
cytotoxic
effects.In
recent
years,
CAR-T
has
achieved
remarkable
successes
treating
hematologic
malignancies;
however,
effects
solid
tumors
not
up
expectations
including
cancer.This
review
aims
discuss
development
preclinical
studies
ongoing
trials.Specifically,
we
summarize
tumor-associated
cancer,
trials,
obstacles
interfering
therapy,
potential
strategies
improve
efficacy.Overall,
hope
our
provides
landscape
view
progress
for
ignites
interest
further
research
directions.
Genes,
Год журнала:
2023,
Номер
14(7), С. 1364 - 1364
Опубликована: Июнь 28, 2023
Breast
cancer
is
the
second
most
frequent
in
world.
It
a
heterogeneous
disease
and
leading
cause
of
mortality
women.
Advances
molecular
technologies
allowed
for
identification
new
more
specifics
biomarkers
breast
diagnosis,
prognosis,
risk
prediction,
enabling
personalized
treatments,
improving
therapy,
preventing
overtreatment,
undertreatment,
incorrect
treatment.
Several
have
been
identified
and,
along
with
traditional
biomarkers,
they
can
assist
physicians
throughout
treatment
plan
increase
therapy
success.
Despite
need
data
to
improve
specificity
determine
real
clinical
utility
some
others
are
already
established
be
used
as
guide
make
decisions.
In
this
review,
we
summarize
available
traditional,
novel,
potential
while
also
including
gene
expression
profiles,
single-cell
polyploid
giant
cells.
We
hope
help
understand
tumor
specific
characteristics
support
decision-making
patient-personalized
management,
consequently
outcome.
Medicina,
Год журнала:
2024,
Номер
60(1), С. 168 - 168
Опубликована: Янв. 17, 2024
Breast
cancer
is
a
prevalent
malignancy
in
the
present
day,
particularly
affecting
women
as
one
of
most
common
forms
cancer.
A
significant
portion
patients
initially
with
localized
disease,
for
which
curative
treatments
are
pursued.
Conversely,
another
substantial
segment
diagnosed
metastatic
has
worse
prognosis.
Recent
years
have
witnessed
profound
transformation
prognosis
this
latter
group,
primarily
due
to
discovery
various
biomarkers
and
emergence
targeted
therapies.
These
biomarkers,
encompassing
serological,
histological,
genetic
indicators,
demonstrated
their
value
across
multiple
aspects
breast
management.
They
play
crucial
roles
initial
diagnosis,
aiding
detection
relapses
during
follow-up,
guiding
application
treatments,
offering
valuable
insights
prognostic
stratification,
especially
highly
aggressive
tumor
types.
Molecular
markers
now
become
keystone
given
diverse
array
chemotherapy
options
treatment
modalities
available.
signify
transformative
shift
arsenal
therapeutic
against
Their
diagnostic
precision
enables
categorization
tumors
elevated
risks
recurrence,
increased
aggressiveness,
heightened
mortality.
Furthermore,
existence
therapies
tailored
target
specific
molecular
anomalies
triggers
cascade
changes
behavior.
Therefore,
primary
objective
article
offer
comprehensive
review
clinical,
diagnostic,
prognostic,
utility
principal
currently
use,
well
clinical
impact
on
In
doing
so,
our
goal
contribute
more
comprehension
complex
disease
and,
ultimately,
enhance
patient
outcomes
through
precise
effective
strategies.
Journal of Personalized Medicine,
Год журнала:
2024,
Номер
14(7), С. 723 - 723
Опубликована: Июль 4, 2024
Breast
cancer
remains
the
most
prevalent
among
women
worldwide,
driving
urgent
need
for
innovative
approaches
to
diagnosis
and
treatment.
This
review
highlights
pivotal
role
of
nanoparticles
in
revolutionizing
breast
management
through
advancements
interconnected
including
targeted
therapy,
imaging,
personalized
medicine.
Nanoparticles,
with
their
unique
physicochemical
properties,
have
shown
significant
promise
addressing
current
treatment
limitations
such
as
drug
resistance
nonspecific
systemic
distribution.
Applications
range
from
enhancing
delivery
systems
sustained
release
developing
diagnostic
tools
early
precise
detection
metastases.
Moreover,
integration
into
photothermal
therapy
synergistic
use
existing
treatments,
immunotherapy,
illustrate
transformative
potential
care.
However,
journey
towards
clinical
adoption
is
fraught
challenges,
chemical
feasibility,
biodistribution,
efficacy,
safety
concerns,
scalability,
regulatory
hurdles.
delves
state
nanoparticle
research,
applications
diagnosis,
obstacles
that
must
be
overcome
integration.
Scientific Reports,
Год журнала:
2025,
Номер
15(1)
Опубликована: Янв. 17, 2025
Breast
cancer
is
the
most
common
malignant
tumor
in
world,
and
its
metastasis
main
cause
of
death
breast
patients.
However,
differences
between
primary
tissue
lymphatic
node,
bone,
brain
metastases
at
single-cell
level
are
not
fully
understood.
We
analyzed
microenvironment
heterogeneity
samples
(n
=
4),
node
3),
bone
2)
using
sequencing
data
from
GEO
database.
The
epithelial
cells
were
characterized
by
InferCNV
algorithm.
cell-cell
communication
was
CellChat
package.
biological
function
cell
subpopulations
gene
set
variation
analysis.
expression
STMN1
immunohistochemical
staining.
proportion
pCAFs
explored
multispectral
identified
seven
clusters
metastatic
(Lymphatic
brain,
metastases)
analyzing
transcriptomic
profiles.
T-NK
B
dominated
with
metastasis,
whereas
fibroblasts
prevalent
cancer.
five
T
(T
memory,
CD8
+
cells,
regulatory
natural
killer
CD4
cells),
three
(naïve
memory
plasma
cancer-associated
(CAFs)
(Smooth
muscle
(SMC),
pericyte,
antigen-presenting
CAFs
(apCAFs),
proliferative
(pCAFs),
matrix
(mCAFs)).
Notably.
metastasis.
Furthermore,
we
four
subpopulations:
G0,
G1,
G2,
G3.
G2
population
exhibited
strong
invasion
ability,
it
can
differentiate
into
G3
ability
proliferation-related
G1
after
Cell-cell
demonstrated
an
interaction
metastasis-associated
cells.
Finally,
discovered
that
advanced
cancer,
pCAF
increased
associated
a
poor
prognosis
This
study
elucidated
potential
cellular
origins
drivers
to
nodes,
utilizing
prognosis.
World Journal of Oncology,
Год журнала:
2025,
Номер
16(1), С. 120 - 130
Опубликована: Янв. 14, 2025
Vascular
endothelial
growth
factor-A
(VEGFA)
is
a
key
inducer
of
angiogenesis,
responsible
for
generating
new
blood
vessels
in
the
tumor
microenvironment
(TME)
and
facilitating
metastasis.
Notably,
Avastin,
which
targets
VEGFA,
failed
to
demonstrate
any
significant
benefit
clinical
trials
breast
cancer
(BC).
This
study
aimed
investigate
relevance
VEGFA
gene
expression
BC.
A
total
7,336
BC
patients
across
eight
independent
cohorts:
ISPY2
(GSE173839),
Sweden
Cancerome
Analysis
Network-Breast
(SCAN-B)
(GSE96058),
Molecular
Taxonomy
Breast
Cancer
International
Consortium
(METABRIC),
GSE25066,
GSE163882,
GSE34138,
GSE20194,
The
Genome
Atlas
(TCGA),
were
analyzed.
calculated
median
level
was
used
stratify
these
cohorts
into
high
low
groups.
High
associated
with
worse
disease-free,
disease-specific,
overall
survival
METABRIC
cohort,
findings
supported
by
SCAN-B
also
showed
(all
P
<
0.02).
seen
triple-negative
(TNBC)
but
not
lymph
node
Additionally,
there
correlation
between
higher
silent
non-silent
mutations,
single-nucleotide
variant
(SNV)
neoantigens,
homologous
recombination
defect,
intratumoral
heterogeneity,
TCGA
cohort.
In
TCGA,
METABRIC,
cohorts,
cell
proliferation:
Ki67
expression,
Nottingham
histological
grade,
consistent
enrichment
all
Hallmark
proliferation-related
sets.
Unexpectedly,
angiogenesis
set
enriched
no
association
infiltrations
lymphatic
or
vascular
cells
besides
pericytes.
had
significantly
less
infiltration
anti-cancer
immune
pro-cancer
cohorts.
Interestingly,
BC,
pathological
complete
response
(pCR)
after
anthracycline-
taxane-based
neoadjuvant
therapy,
heightened
both
estrogen
receptor
(ER)+/human
epidermal
factor
2
(HER2)-
TNBC
subtypes
GSE25066
cohort
immunotherapy
ER+/
HER2-
subtype,
Our
research
indicates
that
confers
proliferation,
reduced
infiltration,
poorer
survival,
allows
better
chemotherapy,
immunotherapy.
Cancers,
Год журнала:
2021,
Номер
13(21), С. 5567 - 5567
Опубликована: Ноя. 7, 2021
Over
the
last
few
years,
a
great
advance
has
been
made
in
comprehension
of
molecular
pathogenesis
underlying
thyroid
cancer
progression,
particularly
for
papillary
(PTC),
which
represents
most
common
malignancy.
Putative
driver
mutations
have
identified
more
than
98%
PTC,
and
new
PTC
classification
into
subtypes
proposed
order
to
resolve
clinical
uncertainties
still
present
management
patients.
Additionally,
prognostic
stratification
systems
profoundly
modified
over
decade,
with
view
refine
patients'
staging
being
able
choose
approach
tailored
on
single
patient's
needs.
Here,
we
will
briefly
discuss
recent
changes
nodules,
review
current
patients
by
analyzing
promising
clinicopathological
features
(i.e.,
gender,
auto-immunity,
multifocality,
histological
variants,
vascular
invasion)
as
well
markers
BRAF/TERT
promoter
mutations,
miRNAs,
components
plasminogen
activating
system)
potentially
capable
ameliorating
prognosis