The
discovery
of
Disulfidptosis
as
a
novel
form
cell
death
has
provided
new
insights
for
the
treatment
cancer
and
various
diseases.
Osteosarcoma
rhabdomyosarcoma
are
malignant
sarcomas
that
predominantly
affect
children,
but
molecular
mechanisms
underlying
development
these
diseases
remain
unclear.
Therefore,
our
study
aimed
to
investigate
involvement
in
both
osteosarcoma
rhabdomyosarcoma.
To
accomplish
this,
we
analyzed
bulk
RNA
transcriptome
sequencing
data
obtained
from
Gene
Expression
Omnibus
(GEO)
datasets
Therapeutically
Applicable
Research
Generate
Effective
Treatments
(TARGET)
databases.
By
employing
non-negative
matrix
factorization
(NMF),
successfully
identified
an
immunosuppressive
subtype
based
on
genes
associated
with
Disulfidptosis.
Notably,
this
exhibited
poor
immune
infiltration.
Furthermore,
employed
combination
100
machine
learning
algorithms
identify
five
most
representative
related
Disulfidptosis:
ACTN4,
MYH9,
FLNA,
MYH10,
IQGAP1.
These
played
crucial
role
characterizing
subtypes
determining
patient's
risk
score.
Particularly,
IQGAP1
independent
prognostic
effects
showed
promise
potential
therapeutic
target
marker.
Additionally,
findings
suggested
strong
association
between
macrophages
Disulfidptosis,
which
may
further
impact
prognosis
patients
osteosarcoma.
Genes,
Journal Year:
2025,
Volume and Issue:
16(5), P. 517 - 517
Published: April 29, 2025
Background:
Cisplatin
resistance
is
a
major
cause
of
tumor
recurrence
and
mortality
in
high-grade
serous
ovarian
cancer
(HGSOC).
Extrachromosomal
circular
DNA
(eccDNA)
has
emerged
as
critical
factor
evolution
drug
resistance.
However,
the
specific
contribution
eccDNA
to
cisplatin
HGSOC
remains
unclear.
Methods:
We
performed
whole-genome
sequencing,
Circle-Seq,
RNA-Seq
four
pairs
primary
cisplatin-resistant
(cisR)
cell
lines
characterize
genome-wide
distribution
features.
Functional
enrichment
analyses
were
subsequently
conducted
on
differentially
expressed
eccDNA-related
genes.
Results:
In
SKOV3
cisR
line,
we
identified
large
extrachromosomal
(ecDNA)
carrying
HIF1A
gene,
which
regulates
repair,
efflux,
epithelial–mesenchymal
transition,
contributing
Using
detected
total
161,062
eccDNAs,
most
less
than
1000
bp
distributed
across
all
chromosomes.
Notably,
number
eccDNAs
chromosome
21
differed
significantly
between
lines.
Additionally,
predominantly
located
non-coding
repetitive
elements.
analysis
genes
revealed
that,
compared
lines,
associated
with
mitotic
spindle
assembly,
regulation
vascular
permeability,
differentiation.
involved
these
pathways
include
MISP,
WIPF1,
RHOD,
KRT80,
PLVAP.
Conclusions:
Our
findings
suggest
that
particularly
ecDNA
amplifications
like
HIF1A,
contribute
mechanisms
HGSOC.
These
insights
highlight
potential
target
for
overcoming
therapeutic
improving
treatment
outcomes
cancer.
Extracellular
vesicles
(EVs)
are
lipid
bilayer-enclosed
released
by
cells.
EVs
encapsulate
proteins
and
nucleic
acids
of
their
parental
cell
efficiently
deliver
the
cargo
to
recipient
These
act
as
mediators
intercellular
communication
thus
play
a
crucial
role
in
various
physiological
pathological
processes.
Moreover,
hold
promise
for
clinical
use.
They
have
been
explored
drug
delivery
vehicles,
therapeutic
agents,
targets
disease
diagnosis.
In
landscape
cancer
research,
while
strides
made
EV-focused
physiopathology,
liquid
biopsy,
delivery,
exploration
immunotherapeutic
agents
may
not
seen
substantial
progress
date.
Despite
promising
findings
reported
animal
studies,
translation
EV-based
immunotherapeutics
encounters
challenges.
Here,
we
review
existing
strategies
used
immunotherapy,
aiming
propel
development
this
emerging
yet
field.
International Journal of Oncology,
Journal Year:
2024,
Volume and Issue:
65(4)
Published: Sept. 5, 2024
Hepatocellular
carcinoma
(HCC)
tissue
is
rich
in
dendritic
cells,
T
B
macrophages,
natural
killer
cells
and
cellular
stroma.
Together
they
form
the
tumor
microenvironment
(TME),
which
also
numerous
cytokines.
Tumor‑associated
macrophages
(TAMs)
are
involved
regulation
of
development.
TAMs
HCC
receive
stimuli
different
directions,
polarize
directions
release
cytokines
to
regulate
development
HCC.
mostly
divided
into
two
cell
phenotypes:
M1
M2.
secrete
pro‑inflammatory
mediators,
M2
a
variety
anti‑inflammatory
pro‑tumorigenic
substances.
The
TAM
polarization
tumors
Both
direct
indirect
methods
for
discussed.
indirectly
support
by
promoting
peripheral
angiogenesis
regulating
immune
TME.
In
terms
between
present
review
mainly
focuses
on
molecular
mechanism.
both
proliferation
apoptosis
quantitative
changes
HCC,
stimulate
related
invasive
migratory
ability
stemness
cells.
aims
identify
immunotherapeutic
options
based
mechanisms
TME
Pharmaceutics,
Journal Year:
2023,
Volume and Issue:
15(10), P. 2460 - 2460
Published: Oct. 13, 2023
Hepatocellular
carcinoma
(HCC)
stands
as
a
significant
contributor
to
global
cancer-related
mortality.
Chronic
inflammation,
often
arising
from
diverse
sources
such
viral
hepatitis,
alcohol
misuse,
nonalcoholic
fatty
liver
disease
(NAFLD),
and
steatohepatitis
(NASH),
profoundly
influences
HCC
development.
Within
this
context,
the
interplay
of
extracellular
vesicles
(EVs)
gains
prominence.
EVs,
encompassing
exosomes
microvesicles,
mediate
cell-to-cell
communication
cargo
transfer,
impacting
various
biological
processes,
including
inflammation
cancer
progression.
Toll-like
receptor
4
(TLR4),
key
sentinel
innate
immune
system,
recognizes
both
pathogen-associated
molecular
patterns
(PAMPs)
damage-associated
(DAMPs),
thereby
triggering
signaling
cascades
pro-inflammatory
cytokine
release.
The
intricate
involvement
TLR4
pathway
in
chronic
pathogenesis
is
discussed
study.
Moreover,
we
delve
into
therapeutic
potential
modulating
using
EVs
novel
agents
for
HCC.
This
review
underscores
multifaceted
role
context
proposes
innovative
avenues
targeted
interventions
against
formidable
disease.
Current Oncology,
Journal Year:
2024,
Volume and Issue:
31(5), P. 2769 - 2779
Published: May 14, 2024
Gastric
cancer
is
the
fifth
most
common
and
fourth
cause
of
global
mortality.
The
identification
new
biomarkers
drug
targets
crucial
to
allow
better
prognosis
treatment
patients.
mitotic
spindle
positioning
(MISP)
protein
has
function
correcting
centrosome
clustering
been
implicated
in
cytokinesis
migration
cells.
goal
this
work
was
evaluate
expression
clinical
relevance
MISP
gastric
cancer.
evaluated
by
immunohistochemistry
a
single
hospital
series
(n
=
286)
adenocarcinomas
compared
with
normal
mucosa
intestinal
metaplasia,
preneoplastic
lesion.
detected
on
membrane
83%
cases,
being
overexpressed
10).
Its
negatively
associated
diffuse
poorly
cohesive
types.
On
other
hand,
it
strongly
expressed
metaplasia
where
MUC2
CDX2
expression.
Furthermore,
when
we
silenced
vitro,
significant
decrease
viability
carcinoma
cells
observed.
In
conclusion,
cancer,
an
phenotype
carcinogenesis
having
role
cellular
proliferation.
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(23), P. 13167 - 13167
Published: Dec. 7, 2024
Hepatocellular
carcinoma
(HCC)
represents
a
significant
clinical
burden
globally
and
is
predicted
to
continue
increase
in
incidence
for
the
foreseeable
future.
The
treatment
of
HCC
complicated
by
fact
that,
majority
cases,
it
develops
on
background
advanced
chronic
inflammatory
liver
disease.
Chronic
inflammation
can
foster
an
immunosuppressive
microenvironment
that
promotes
tumour
progression
metastasis.
In
this
setting,
macrophages
make
up
major
immune
component
microenvironment,
review,
we
focus
their
contribution
development
progression.
Tumour-associated
(TAMs)
are
largely
derived
from
infiltrating
monocytes
potent
anti-inflammatory
phenotype
be
induced
factors
found
within
such
as
growth
factors,
cytokines,
hypoxia,
extracellular
matrix
(ECM)
proteins.
general,
experimental
evidence
suggest
TAMs
exhibit
variety
functions
aid
progression,
including
promotion
angiogenesis,
resistance
drug
therapy,
releasing
support
cell
proliferation
Despite
tumour-promoting
profile,
there
underlying
plasticity
these
cells
targeted
help
reprogramme
drive
tumour-specific
responses.
We
discuss
potential
targeting
therapeutically
either
altering
or
therapy
approaches
taking
advantage
infiltrative
properties
circulation
into
tissue.
Viruses,
Journal Year:
2024,
Volume and Issue:
16(11), P. 1785 - 1785
Published: Nov. 17, 2024
Extracellular
vesicles
(EVs)
are
bilayer
released
by
cells
in
the
microenvironment
of
liver
including
parenchymal
and
non-parenchymal
cells.
They
third
important
mechanism
communications
between
cells,
besides
secretion
cytokines
chemokines
direct
cell-to-cell
contact.
The
aim
this
review
is
to
discuss
role
EVs
viral
disease,
as
there
increasing
evidence
that
transportation
proteins,
all
types
RNA,
particles
complete
virions
implicated
pathogenesis
both
cirrhosis
viral-related
hepatocellular
carcinoma.
biogenesis
discussed
their
diseases
presented.
Their
use
diagnostic
prognostic
biomarkers
also
analyzed.
Most
importantly,
significance
possible
novel
treatment
strategies
for
fibrosis
carcinoma
presented,
although
available
data
based
on
experimental
clinical
trials
have
not
been
reported.