PubMed,
Год журнала:
2023,
Номер
26(9), С. 701 - 708
Опубликована: Сен. 20, 2023
The
genomic
instability
may
lead
to
an
initiation
of
cancer
in
many
organisms.
Homologous
recombination
repair
(HRR)
is
vital
maintaining
cellular
stability.
RAD51
associated
protein
1
(RAD51AP1),
which
plays
a
crucial
role
HRR
and
primarily
participates
forming
D-loop,
was
reported
as
essential
for
However,
recent
studies
showed
that
RAD51AP1
significantly
overexpressed
various
types
correlated
with
poor
prognosis.
These
results
suggested
play
significant
pro-cancer
effect
multiple
cancers.
underlying
mechanism
still
unclear.
Cancer
stemness-maintaining
effects
might
be
considered
the
most
reliable
mechanism.
Meanwhile,
also
promoted
resistance
radiation
therapy
chemotherapy
Thus,
researches
focused
on
RAD51AP1,
its
regulatory
molecules
provide
new
targets
overcoming
progression
treatment
resistance.
Here,
we
reviewed
latest
research
cancers
summarized
differential
expression
prognostic
implications.
In
this
review,
outlined
potential
mechanisms
drug
resistance-promoting
several
directions
further
research.
.【中文题目:RAD51AP1在肿瘤进展和耐药中的研究进展】
【中文摘要:基因组失稳可能导致多种肿瘤的发生发展。同源性重组修复(homologous
repair,
HRR)是机体维持基因组稳态的重要机制之一。RAD51相关蛋白1(RAD51
1,
RAD51AP1)在HRR中至关重要,其主要参与D-loop的形成,是维持细胞基因组稳态的重要分子。然而,据文献报道RAD51AP1在多种癌种中显著高表达,并与预后呈负相关,提示其可能具有显著的促癌作用。其促癌作用机制尚不明确,可能与肿瘤干性密切相关。同时,RAD51AP1还在放疗和化疗的耐药中具有重要作用。探索RAD51AP1和其上下游调控机制可能能够找寻逆转肿瘤治疗耐药的新靶点。因此,我们综述了目前关于RAD51AP1在肿瘤中的研究,归纳了其在各种肿瘤中的差异表达及与预后的关系,总结了其促癌作用的潜在机制,分析了其促进耐药相关研究的现状,旨在为后续寻找抑制肿瘤进展和逆转耐药的靶点的研究提供一定的方向。
】
【中文关键词:RAD51AP1;肿瘤干细胞;耐药】.
Cancer Medicine,
Год журнала:
2023,
Номер
12(18), С. 18960 - 18980
Опубликована: Сен. 1, 2023
Abstract
Accumulating
data
reveals
that
tumors
possess
a
specialized
subset
of
cancer
cells
named
stem
(CSCs),
responsible
for
metastasis
and
recurrence
malignancies,
with
various
properties
such
as
self‐renewal,
heterogenicity,
capacity
drug
resistance.
Some
signaling
pathways
or
processes
like
Notch,
epithelial
to
mesenchymal
transition
(EMT),
Hedgehog
(Hh),
Wnt,
well
CSCs'
surface
markers
CD44,
CD123,
CD133,
cell
adhesion
molecule
(EpCAM)
have
pivotal
roles
in
acquiring
CSCs
properties.
Therefore,
targeting
CSC‐related
might
effectively
eradicate
pave
the
way
survival.
Since
current
treatments
chemotherapy
radiation
therapy
cannot
all
tumor
relapse
may
happen
following
temporary
recovery,
improving
novel
more
efficient
therapeutic
options
combine
is
required.
Immunotherapy
strategies
are
new
modalities
promising
results
CSCs.
Here,
we
review
by
immunotherapy
dendritic
(DC)
vaccines,
chimeric
antigen
receptors
(CAR)‐engineered
immune
cells,
natural
killer‐cell
(NK‐cell)
therapy,
monoclonal
antibodies
(mAbs),
checkpoint
inhibitors,
use
oncolytic
viruses
(OVs)
pre‐clinical
clinical
studies.
This
will
mainly
focus
on
blood
malignancies
but
also
describe
solid
cancers.
Frontiers in Immunology,
Год журнала:
2024,
Номер
15
Опубликована: Май 31, 2024
CD24
is
a
glycosylphosphatidylinositol-anchored
protein
that
expressed
in
wide
range
of
tissues
and
cell
types.
It
involved
variety
physiological
pathological
processes,
including
adhesion,
migration,
differentiation,
apoptosis.
Additionally,
has
been
studied
extensively
the
context
cancer,
where
it
found
to
play
role
tumor
growth,
invasion,
metastasis.
In
recent
years,
there
growing
interest
as
potential
therapeutic
target
for
cancer
treatment.
This
review
summarizes
current
knowledge
CD24,
its
structure,
function,
cancer.
Finally,
we
provide
insights
into
clinical
application
discuss
possible
approaches
development
targeted
therapies.
ACS Omega,
Год журнала:
2025,
Номер
10(12), С. 12109 - 12121
Опубликована: Март 6, 2025
Transitional
cold
atmospheric
plasma
(TCAP)
represents
a
novel
technique
for
generating
remotely
from
primary
source.
It
consists
of
partially
nonthermal
ionized
gas
mixture
containing
charged
and
neutral
particles,
photons,
free
radicals.
In
recent
years,
TCAP
has
attracted
considerable
attention
in
biomedical
applications.
order
to
evaluate
colon
cancer
stem
cells'
(CCSCs)
proliferation,
apoptotic
induction,
inflammatory
response,
survival,
was
utilized
both
directly
indirectly
this
study.
Using
argon
helium
gases,
continuously
delivered
two
stages
during
the
experiment.
For
direct
state,
irradiated
onto
CCSCs
3
5
min.
indirect
technique,
Matrigel
treated
with
min
before
introduction
cells.
vitro
assays
demonstrated
that
exposure
significantly
reduced
viability
CCSCs;
application
had
greater
impacts
than
argon.
Numerous
investigations
confirmed
induction
apoptosis,
showing
groups
more
cells
altered
cellular
structures
controls
(****p
<
0.0001).
A
substantial
increase
Bax/Bcl-2
ratio
found
by
analyzing
expression
Bax
Bcl-2
genes,
indicating
increased
susceptibility
apoptosis
(*p
=
0.0177
***p
0.0004).
The
higher
efficacy
mode
further
highlighted
marker
analysis,
which
showed
significant
reduction
interleukin-6
interleukin-8
TCAP-helium
compared
TCAP-argon
(**p
0.0015
0.0007).
Lastly,
proliferation
test,
relies
on
Ki-67
expression,
noteworthy
decline
all
TCAP-treated
groups,
group
exhibiting
most
robust
impact
0.0014).
Overall,
findings
highlight
potential
TCAP,
particularly
helium,
as
promising
approach
selectively
targeting
providing
insights
into
its
therapeutic
mechanisms
treatment.
therefore,
emerges
unique
strategy
applications
cell-targeted
therapies.
Molecular Biomedicine,
Год журнала:
2024,
Номер
5(1)
Опубликована: Дек. 31, 2024
Lenvatinib,
an
approved
first-line
regimen,
has
been
widely
applied
in
hepatocellular
carcinoma
(HCC).
However,
clinical
response
towards
Lenvatinib
was
limited,
emphasizing
the
importance
of
understanding
underlying
mechanism
its
resistance.
Herein,
we
employed
integrated
bioinformatic
analysis
to
identify
calpain-2
(CAPN2)
as
a
novel
key
regulator
for
resistance
HCC,
and
expression
greatly
increased
both
Lenvatinib-resistant
HCC
cell
lines
samples.
Further
vitro
vivo
experiments
indicated
that
knocking
down
CAPN2
sensitized
cells
treatment,
while
overexpression
achieved
opposite
effects
Lenvatinib-sensitive
line.
Interestingly,
observed
close
relationship
between
cancer
stem
(CSC)
traits
cells,
evidenced
by
impaired
sphere-forming
CSC-related
marker
expressions
after
knockdown,
verse
vice.
Mechanistically,
strikingly
discovered
exerted
function
enzyme-dependent
enzyme-independent
manner
simultaneously:
activating
β-Catenin
signaling
through
enzyme
activity,
preventing
GLI1/GLI2
degradation
direct
binding
YWHAE
manner,
which
disrupting
association
inhibit
YWHAE-induced
GLIs.
Notably,
further
co-immunoprecipitation
assays
revealed
could
promote
protein
stability
via
recruiting
deubiquitinase
COPS5
prevent
ubiquitination-induced
CAPN2.
In
summary,
our
data
demonstrated
promoted
catalytic
activity-dependent
-independent
approaches.
Reducing
rather
than
inhibiting
activity
might
be
promising
strategy
improve
treatment
efficiency
HCC.
Biomedicine & Pharmacotherapy,
Год журнала:
2023,
Номер
170, С. 116043 - 116043
Опубликована: Дек. 20, 2023
Cancer
stem
cells
are
the
key
link
between
malignant
tumor
progression
and
drug
resistance.
This
cell
population
has
special
properties
that
different
from
those
of
conventional
cells,
role
cancer
cell-related
exosomes
in
malignancy
is
becoming
increasingly
clear.
cell-derived
carry
a
variety
functional
molecules
involved
regulation
microenvironment,
especially
with
regard
to
immune
but
how
these
exert
their
functions
specific
mechanisms
need
be
further
clarified.
Here,
we
summarize
regulating
detail,
aiming
provide
new
insights
for
subsequent
targeted
development
clinical
strategy
formulation.
Translational Cancer Research,
Год журнала:
2024,
Номер
13(6), С. 2971 - 2984
Опубликована: Июнь 1, 2024
Esophageal
squamous
cell
carcinoma
(ESCC),
a
prevalent
malignancy
within
the
upper
gastrointestinal
system,
is
characterized
by
its
unfavorable
prognosis
and
absence
of
specific
indicators
for
outcome
prediction
high-risk
case
identification.
In
our
research,
we
examined
expression
levels
cancer
stem
cells
(CSCs),
markers
CD44/SOX2
in
ESCC,
scrutinized
their
association
with
clinicopathological
parameters,
developed
predictive
nomogram
model.
This
model,
which
incorporates
CD44/SOX2,
aims
to
forecast
overall
survival
(OS)
patients
afflicted
ESCC.
Frontiers in Molecular Biosciences,
Год журнала:
2024,
Номер
10
Опубликована: Фев. 22, 2024
The
cancer
stem
cells
are
a
rare
group
of
self-renewable
capable
the
initiation,
progression,
metastasis
and
recurrence
tumors,
also
key
contributor
to
therapeutic
resistance.
Thus,
understanding
molecular
mechanism
tumor
stemness
regulation,
especially
in
gastrointestinal
(GI)
cancers,
is
great
importance
for
targeting
CSC
designing
novel
strategies.
This
review
aims
elucidate
current
advancements
including
biomarkers,
signaling
pathways,
non-coding
RNAs.
We
will
provide
comprehensive
view
on
how
microenvironment
(TME)
display
an
overall
tumor-promoting
effect,
recruitment
impact
cancer-associated
fibroblasts
(CAFs),
establishment
immunosuppressive
milieu,
induction
angiogenesis
hypoxia.
Lastly,
this
consolidates
mainstream
interventions
regulation.