Frontiers in Bioscience-Landmark,
Год журнала:
2024,
Номер
29(11)
Опубликована: Ноя. 20, 2024
Lysosomes
are
essential
intracellular
catabolic
organelles
that
contain
digestive
enzymes
involved
in
the
degradation
and
recycle
of
damaged
proteins,
organelles,
etc.
Thus,
they
play
an
important
role
various
biological
processes,
including
autophagy
regulation,
ion
homeostasis,
cell
death,
senescence.
A
myriad
studies
has
shown
dysfunction
lysosome
is
implicated
human
aging
age-related
diseases,
cancer.
However,
what
noteworthy
modulation
lysosome-based
signaling
both
cancer-suppressive
cancer-promotive
functions
diverse
cancers
depending
on
stage,
biology,
or
tumor
microenvironment.
This
dual
limits
their
application
as
targets
cancer
therapy.
In
this
review,
we
provide
overview
autophagy-lysosomal
pathway
outline
critical
roles
many
cellular
death.
We
highlight
different
development
progression,
underscoring
its
potential
a
target
for
effective
therapies.
Cell
death
is
a
fundamental
part
of
life
for
metazoans.
To
maintain
the
balance
between
cell
proliferation
and
metabolism
human
bodies,
certain
number
cells
need
to
be
removed
regularly.
Hence,
mechanisms
have
been
preserved
during
evolution
multicellular
organisms.
Tumorigenesis
closely
related
with
exceptional
inhibition
death.
Mutations
or
defects
in
death-related
genes
block
elimination
abnormal
enhance
resistance
malignant
chemotherapy.
Therefore,
investigation
enables
development
drugs
that
directly
induce
tumor
In
guidelines
updated
by
Death
Nomenclature
Committee
(NCCD)
2018,
was
classified
into
12
types
according
morphological,
biochemical
functional
classification,
including
intrinsic
apoptosis,
extrinsic
mitochondrial
permeability
transition
(MPT)-driven
necrosis,
necroptosis,
ferroptosis,
pyroptosis,
PARP-1
parthanatos,
entotic
death,
NETotic
lysosome-dependent
autophagy-dependent
immunogenic
cellular
senescence
mitotic
catastrophe.
The
mechanistic
relationships
epigenetic
controls
cancer
progression
were
previously
unclear.
this
review,
we
will
summarize
pathways
corresponding
regulations.
Also,
explore
extensive
interactions
these
discuss
epigenetics
which
bring
benefits
therapy.
Holistic Integrative Oncology,
Год журнала:
2025,
Номер
4(1)
Опубликована: Янв. 13, 2025
Abstract
There
are
numerous
types
of
orbital
tumors,
among
which
ameloblastoma
is
a
rare
metastatic
benign
tumor
that
often
originates
in
the
jaw
and
later
metastasizes
to
orbit.
The
mystery
it
lies
that,
although
classified
as
tumor,
exhibits
high
recurrence
malignant
potential
with
invasiveness,
posing
serious
threat
ocular
health
quality
life
patients.
prognosis
relatively
poor,
but
there
still
hope.
With
aggressive
treatment
close
follow-up
observation,
patients
may
have
possibility
achieving
longer
survival
period
better
life.
global
incidence
0.92
cases
per
million
people
year.
According
world
literature
reports,
32
maxillary
bone
metastasis
orbit
4
mandibular
more
related
research
being
reported,
necessary
comprehensively
review
etiology,
clinical
manifestations,
diagnosis,
treatment,
ameloblastoma,
order
enhance
ophthalmologists'
understanding
diagnostic
skills
this
disease,
ultimately
improve
patients'
Background:
Ionizing
radiation
(IR)
is
a
well-known
inducer
of
cellular
senescence
and
the
senescence-associated
secretory
phenotype
(SASP).
SASP
factors
play
dual
roles
in
cancer,
either
promoting
or
inhibiting
its
development.
This
study
investigates
IR-induced
specifically
secreted
by
renal
cortical
epithelial
(RCE)
cells
their
role
cell
carcinoma
(RCC)
progression.
Methods:
Proteomic
data
from
Atlas
were
analyzed
to
identify
unique
RCE
cells,
with
subsequent
evaluations
performed
at
both
gene
protein
levels.
Thirty-seven
proteins
identified
as
exclusively
upregulated
senescent
cells.
Gene
expression
analysis
these
RCE-specific
was
conducted
using
Expression
database
Normal
Tumor
tissues
(GENT2)
The
Cancer
Genome
(TCGA).
To
assess
prognostic
relevance
RCC,
corresponding
further
Human
Protein
(HPA),
emphasizing
relationship
between
factor
RCC
Results:
ALDH18A1
ASPH
emerged
key
significant
upregulation
levels
(Log2
ratio
>
1.15,
p
<
0.05).
These
are
implicated
pro-cancer
activities
strongly
associated
poor
outcomes
RCC.
Their
critical
progression
underscore
potential
promising
therapeutic
targets
for
prevention
treatment
disease.
Conclusions:
provides
novel
insights
into
carcinogenesis,
marking
first
identification
specific
tumor
suggests
that
hold
promise
early
biomarkers
disease
treatment.
Cells,
Год журнала:
2025,
Номер
14(4), С. 249 - 249
Опубликована: Фев. 10, 2025
Various
stressors
such
as
ionizing
radiation
(IR),
chemotherapeutic
agents,
oxidative
stress,
and
inflammatory
responses
can
trigger
the
stress-induced
premature
senescence
(SIPS)
of
cells
in
bone
microenvironment,
including
osteocytes.
However,
little
is
known
about
mechanisms
underlying
senescent
cellular
regulation
differentiation
potential
homeostasis.
Here,
we
report
a
secretory
change
osteocytes
activated
by
IR,
its
subsequent
impact
on
osteogenic
osteoclastic
differentiation,
cascade
response.
It
was
observed
that
exhibited
altered
biological
function,
persistent
incomplete
DNA
damage
repair,
characteristic
phenotypes
after
exposure
to
IR
vitro.
Meanwhile,
concomitant
increase
CC
chemokine
ligand
3
(CCL3),
key
component
senescence-associated
phenotype
(SASP),
IR-induced
osteocytes,
which
could
further
downregulate
enhance
cell
supernatant
co-culture
experiments.
Notably,
enhancement
PI3K/Akt/NF-κB
signaling
pathway
appears
be
an
essential
driver
imbalance
between
potentials.
Taken
together,
these
data
suggest
novel
role
CCL3
homeostatic
through
SASP
secretion,
mediated
pathway.
International Journal of Molecular Sciences,
Год журнала:
2025,
Номер
26(4), С. 1551 - 1551
Опубликована: Фев. 12, 2025
Mitophagy
plays
a
critical
role
in
maintaining
mitochondrial
quality
and
cellular
homeostasis.
But
the
specific
contribution
of
mitophagy-related
E3
ubiquitin
ligases
to
prognoses
remains
largely
unexplored.
In
this
study,
we
identified
novel
ligase
prognostic
signature
using
least
absolute
shrinkage
selector
operator
(LASSO)
multivariate
Cox
regression
analyses
breast
cancer.
Based
on
median
risk
scores,
patients
were
divided
into
high-risk
low-risk
groups.
Functional
enrichment
conducted
explore
biological
differences
between
two
Immune
infiltration,
drug
sensitivity,
mitochondrial-related
phenotypes
also
analyzed
evaluate
clinical
implications
model.
A
four-gene
(ARIH1,
SIAH2,
UBR5,
WWP2)
was
identified,
Kaplan-Meier
analysis
demonstrated
that
group
had
significantly
worse
overall
survival
(OS).
The
exhibited
disrupted
metabolism
immune
dysregulation
with
upregulated
checkpoint
molecules.
Additionally,
higher
sensitivity
several
drugs
targeting
Akt/PI3K/mTORC1
signaling
axis.
Accompanying
metabolic
dysregulation,
mtDNA
stress
elevated,
contributing
activation
senescence-associated
secretory
phenotype
(SASP)
group.
conclusion,
provides
robust
tool
for
stratification
offers
insights
interplay
mitophagy,
modulation,
therapeutic
responses
Frontiers in Oncology,
Год журнала:
2025,
Номер
15
Опубликована: Март 20, 2025
Background
The
process
of
human
aging
is
accompanied
by
an
increased
susceptibility
to
various
cancers,
including
gastric
cancer.
This
heightened
linked
the
shared
molecular
characteristics
between
and
tumorigenesis.
Autophagy
considered
a
critical
mediator
connecting
cancer,
exerting
dynamic
regulatory
effect
in
conjunction
with
cellular
senescence
during
tumor
progression.
In
this
study,
combined
analysis
autophagy-
senescence-related
genes
was
employed
comprehensively
capture
heterogeneity.
Methods
gene
expression
profiles
clinical
data
for
GC
samples
were
acquired
from
TCGA
GEO
databases.
Differentially
expressed
(DEASRGs)
identified
normal
tissues.
Gene
Ontology
(GO)
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
pathway
analyses
carried
out
provide
insights
into
biological
significance.
A
prognostic
signature
established
using
univariate
Cox
LASSO
regression
analyses.
Furthermore,
consensus
clustering
nomograms
survival
prediction.
TME
drug
sensitivity
conducted
compare
differences
groups.
To
predict
immunotherapy
efficacy,
correlations
risk
score
immune
checkpoints,
MSI,
TMB,
TIDE
scores
investigated.
Results
fourteen-gene
superior
accuracy
constructed.
patients
stratified
three
distinct
clusters,
each
exhibiting
significant
variations
their
prognosis
microenvironments.
Drug
revealed
that
low-risk
group
demonstrated
greater
responsiveness
several
commonly
used
chemotherapeutic
agents
oxaliplatin.
further
indicated
high-risk
exhibited
cell
infiltration,
upregulated
ICs,
higher
stromal
score,
suggesting
capacity
evasion.
contrast,
characterized
proportion
microsatellite
instability-high
(MSI-H)
cases,
elevated
indicating
likelihood
benefiting
immunotherapy.
addition,
Single-cell
sequencing
TXNIP
epithelial
cells.
Cellular
experiments
preliminarily
verified
could
promote
proliferation
migration
cancer
Conclusion
study
presents
robust
predictive
model
genes,
demonstrating
its
ability
effectiveness,
guide
personalized
treatment.
Aging and Disease,
Год журнала:
2025,
Номер
unknown, С. 0 - 0
Опубликована: Янв. 1, 2025
Cellular
senescence
is
the
basic
unit
of
organismal
aging,
a
complicated
biological
process
involving
several
cell
types
and
tissues.
It
also
an
important
mechanism
by
which
body
responds
to
damage
potential
carcinogenesis.
However,
excessive
or
abnormal
cellular
can
lead
tissue
functional
degradation
occurrence
diseases.
In
recent
years,
role
epigenetic
modifications
in
has
received
extensive
attention.
Lactylation,
novel
post-translational
modification
derived
from
lactate,
recently
gained
significant
attention
as
key
factor
metabolism
regulation,
gradually
demonstrating
its
importance
regulation
senescence.
This
review
emphasizes
bidirectional
causal
relationship
between
lactylation
senescence,
highlighting
therapeutic
target
for
aging-related