Unveiling the multifaceted roles of long non-coding RNA CTBP1-DT in human diseases: Special attention to its microprotein-encoding potential
Pathology - Research and Practice,
Год журнала:
2025,
Номер
268, С. 155870 - 155870
Опубликована: Фев. 26, 2025
Язык: Английский
A Comparison of Treatment With Skin Graft or Secondary Healing for Nasal Wound Defects After Tumor Excision: A Randomized Study
Plastic & Reconstructive Surgery Global Open,
Год журнала:
2025,
Номер
13(3), С. e6620 - e6620
Опубликована: Март 1, 2025
A
full-thickness
skin
graft
is
a
commonly
used
method
for
repairing
smaller
nasal
defects.
Secondary
healing
simple
alternative
with
many
advantages,
although
it
associated
long
duration
of
healing.
The
aim
was
to
compare
the
short-
and
long-term
results
transplantation
or
secondary
small
wound
defects
after
tumor
excision.
Adult
patients
admitted
resection
were
randomized
treatment
either
intent.
Healing
complications
assessed
at
1
4
weeks.
Scar
quality
patient
observer
scar
assessment
scale
(POSAS)
6
months
postoperatively.
Twenty-six
included.
Three
healed
within
week
in
group,
whereas
none
had
group
(SHG).
time
(median
[interquartile
range])
35.0
(28.0-41.0)
days
28.0
(12.0-48.0)
SHG
respectively
(P
=
0.47).
Patient-POSAS
scores
reported
better
all
items
(pain,
itching,
color,
stiffness,
thickness,
irregularity),
not
significantly.
Observer-POSAS
vascularity,
pigmentation,
relief
0.003,
0.007,
0.002,
0.01,
respectively).
did
differ
between
2
groups.
cosmetic
outcome
showed
promising
SHG,
suggesting
that
allowing
superficial,
surgery
may
be
beneficial.
However,
strength
this
conclusion
hampered
by
study
group.
Язык: Английский
Exploring cell death pathways in oral cancer: mechanisms, therapeutic strategies, and future perspectives
Discover Oncology,
Год журнала:
2025,
Номер
16(1)
Опубликована: Март 26, 2025
Oral
squamous
cell
carcinoma
(OSCC)
represents
a
significant
global
health
challenge,
characterized
by
aggressive
progression
and
poor
therapeutic
response
despite
advances
in
treatment
modalities.
This
review
provides
comprehensive
analysis
of
diverse
death
mechanisms
OSCC,
encompassing
traditional
pathways
(apoptosis,
autophagy,
necrosis),
newly
(ferroptosis,
pyroptosis,
necroptosis),
emerging
(cuproptosis,
anoikis,
parthanatos,
entosis).
By
examining
the
molecular
basis
these
pathways,
particularly
crucial
roles
p53
signaling
miRNA
regulation,
we
highlight
how
their
dysregulation
contributes
to
resistance
tumor
progression.
The
synthesizes
recent
evidence
demonstrating
complex
interplay
between
ten
distinct
impact
on
microenvironment
immune
response.
We
evaluate
innovative
approaches
that
target
including
novel
small
molecules,
combination
strategies,
immunomodulatory
treatments
exploit
specific
enhance
efficacy.
Special
attention
is
given
personalized
medicine
strategies
consider
individual
characteristics
pathway
profiles.
integrating
current
challenges
with
future
research
directions,
this
framework
for
developing
more
effective
can
leverage
multiple
overcome
therapy
improve
outcomes
oral
cancer
patients.
Язык: Английский
AP1M2 Drives Gemcitabine‐Cisplatin Chemoresistance by Enhancing RAD54B‐Associated DNA Repair in Bladder Cancer
The FASEB Journal,
Год журнала:
2025,
Номер
39(10)
Опубликована: Май 19, 2025
ABSTRACT
The
combination
of
gemcitabine
and
cisplatin
serves
as
a
cornerstone
in
bladder
cancer
(BC)
treatment,
yet
chemotherapy
resistance
continues
to
pose
significant
challenge.
This
study
utilizes
novel
BC
organoid
model
integrated
with
drug
sensitivity
assays
uncover
the
mechanisms
underlying
identify
potential
therapeutic
targets.
Our
findings
reveal
that
AP1M2
expression
is
markedly
upregulated
gemcitabine‐
cisplatin‐resistant
cells
tissues.
Elevated
levels
contribute
enhanced
tumor
cell
proliferation
by
facilitating
DNA
damage
response
increasing
RAD54B
expression.
Mechanistically,
interacts
RNA‐binding
protein
PUM1
stabilize
mRNA,
thereby
supporting
repair
survival
under
chemotherapeutic
stress.
Notably,
inhibition
AP1M2/PUM1‐mediated
sensitized
xenografts
gemcitabine‐cisplatin
treatment
vivo.
These
unveil
mechanism
highlight
AP1M2/PUM1/RAD54B
pathway
promising
target
counter
enhance
outcomes.
Язык: Английский
Fantastic Frogs and Where to Use Them: Unveiling the Hidden Cinobufagin’s Promise in Combating Lung Cancer Development and Progression Through a Systematic Review of Preclinical Evidence
Cancers,
Год журнала:
2024,
Номер
16(22), С. 3758 - 3758
Опубликована: Ноя. 7, 2024
Cinobufagin
(CB),
a
bufadienolide,
has
shown
promising
potential
as
an
anticancer
agent,
particularly
in
combating
lung
cancer.
This
systematic
review
synthesizes
preclinical
evidence
on
CB's
effects
against
cancer,
focusing
its
mechanisms
of
action,
efficacy,
and
clinical
implications.
We
analyzed
data
from
various
studies
involving
both
vitro
cell
line
models
vivo
animal
models.
The
reviewed
indicate
that
CB
effectively
reduces
viability,
induces
apoptosis,
inhibits
proliferation,
migration,
invasion
across
multiple
cancer
lines
xenograft
Specifically,
was
found
to
decrease
viability
increase
apoptosis
cells
by
modulating
key
molecular
pathways,
including
Bcl-2,
Bax,
cleaved
caspases,
caveolin-1,
FLOT2,
Akt,
STAT3,
FOXO1.
In
further
demonstrated
significant
inhibition
tumor
growth
with
minimal
toxicity.
However,
limitations
include
reliance
models,
which
may
not
fully
represent
dynamics,
lack
long-term
safety
data.
also
vary
their
methodologies
accurately
encompass
all
subtypes
or
predict
human
responses.
Despite
these
limitations,
ability
target
specific
pathways
results
suggest
it
could
be
valuable
addition
treatment
strategies.
Our
suggests
trials
validate
efficacy
humans.
Future
research
should
explore
combination
therapies
optimize
delivery
methods
enhance
outcomes.
Язык: Английский