Frontiers in Cell Death,
Journal Year:
2024,
Volume and Issue:
3
Published: July 15, 2024
The
exploration
of
multiple
regulated
cell
death
(RCD)
pathways
and
the
recognition
that
several
death-related
proteins,
including
caspases,
serve
non-canonical
roles
have
significantly
expanded
diversified
research.
Caspases
not
only
cleave
cellular
substrates,
triggering
apoptosis,
but
also
impact
essential
processes
such
as
differentiation,
proliferation,
growth,
migration.
These
novel
caspase-dependent
regulatory
networks
are
extensively
studied
during
development,
with
Drosophila
providing
a
diverse
range
developmental
models
for
investigating
these
phenomena.
Moreover,
recent
insights
into
functions
proteins
highlighted
their
pivotal
role
in
cancer
aggressiveness.
Ultimately,
understanding
sheds
light
on
intricate
connections
between
RCD
significance
promoting
anti-oncogenic
responses.
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: Nov. 6, 2023
Abnormal
cellular
apoptosis
plays
a
pivotal
role
in
the
pathogenesis
of
Multiple
Myeloma
(MM).
Over
years,
BCL-2,
crucial
anti-apoptotic
protein,
has
garnered
significant
attention
MM
therapeutic
research.
Venetoclax
(VTC),
small-molecule
targeted
agent,
effectively
inhibits
promoting
programmed
death
cancerous
cells.
While
VTC
been
employed
to
treat
various
hematological
malignancies,
its
particular
efficacy
showcased
potential
for
broader
clinical
applications.
In
this
review,
we
delve
into
intricacies
how
modulates
cells
by
targeting
BCL-2
and
overarching
influence
protein
family
regulation.
Our
findings
highlight
nuanced
interplay
between
VTC,
MM,
offering
insights
that
may
pave
way
optimizing
strategies.
Through
comprehensive
analysis,
aim
lay
solid
groundwork
future
explorations
VTC’s
applications
profound
effects
on
apoptosis.
MedComm,
Journal Year:
2024,
Volume and Issue:
5(9)
Published: Sept. 1, 2024
Abstract
Cell
death
regulation
is
essential
for
tissue
homeostasis
and
its
dysregulation
often
underlies
cancer
development.
Understanding
the
different
pathways
of
cell
can
provide
novel
therapeutic
strategies
battling
cancer.
This
review
explores
several
key
mechanisms
apoptosis,
necroptosis,
autophagic
death,
ferroptosis,
pyroptosis.
The
research
gap
addressed
involves
a
thorough
analysis
how
these
be
precisely
targeted
therapy,
considering
tumor
heterogeneity
adaptation.
It
delves
into
genetic
epigenetic
factors
signaling
cascades
like
phosphatidylinositol
3‐kinase/protein
kinase
B/mammalian
target
rapamycin
(PI3K/AKT/mTOR)
mitogen‐activated
protein
kinase/extracellular
signal‐regulated
(MAPK/ERK)
pathways,
which
are
critical
death.
Additionally,
interaction
microenvironment
with
cells,
particularly
influence
hypoxia,
nutrient
deprivation,
immune
cellular
interactions,
explored.
Emphasizing
strategies,
this
highlights
emerging
modulators
inducers
such
as
B
lymphoma
2
(BCL2)
homology
domain
3
(BH3)
mimetics,
tumour
necrosis
factor‐related
apoptosis‐inducing
ligand
(TRAIL),
chloroquine,
innovative
approaches
to
induce
ferroptosis
provides
insights
therapy's
future
direction,
focusing
on
multifaceted
circumvent
drug
resistance.
examination
evolving
underlines
considerable
clinical
potential
continuous
necessity
in‐depth
exploration
within
scientific
domain.
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
168, P. 115741 - 115741
Published: Oct. 19, 2023
Acetyl-coenzyme
A
(acetyl-CoA),
an
essential
metabolite,
not
only
takes
part
in
numerous
intracellular
metabolic
processes,
powers
the
tricarboxylic
acid
cycle,
serves
as
a
key
hub
for
biosynthesis
of
fatty
acids
and
isoprenoids,
but
also
signaling
substrate
acetylation
reactions
post-translational
modification
proteins,
which
is
crucial
epigenetic
inheritance
cells.
Acetyl-CoA
links
lipid
metabolism
with
histone
to
create
more
intricate
regulatory
system
that
affects
growth,
aggressiveness,
drug
resistance
malignancies
such
glioblastoma,
breast
cancer,
hepatocellular
carcinoma.
These
fascinating
advances
knowledge
acetyl-CoA
during
carcinogenesis
normal
physiology
have
raised
interest
regarding
its
modulation
malignancies.
In
this
review,
we
provide
overview
regulation
cancer
relevance
main
pathways
participates.
We
summarize
role
reprogramming
stress
cells,
well
medical
application
inhibitors
targeting
dysregulation
therapeutic
intervention
cancers.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(14), P. 11534 - 11534
Published: July 16, 2023
Single
cell
biology
has
revealed
that
solid
tumors
and
tumor-derived
lines
typically
contain
subpopulations
of
cancer
cells
are
readily
distinguishable
from
the
bulk
by
virtue
their
enormous
size.
Such
with
a
highly
enlarged
nucleus,
multiple
nuclei,
and/or
micronuclei
often
referred
to
as
polyploid
giant
(PGCCs),
may
exhibit
features
senescence.
PGCCs
enter
dormant
phase
(active
sleep)
after
they
formed,
but
subset
remain
viable,
secrete
growth
promoting
factors,
can
give
rise
therapy
resistant
tumor
repopulating
progeny.
Here
we
will
briefly
discuss
prevalence
prognostic
value
across
different
types,
current
understanding
mechanisms
formation
fate,
possible
reasons
why
these
“monsters”
continue
be
ignored
in
most
therapy-related
preclinical
studies.
In
addition
PGCCs,
other
within
(such
oncogenic
caspase
3-activated
drug-tolerant
persister
cells)
also
contribute
resistance
pose
major
challenges
delivery
therapy.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(20), P. 4994 - 4994
Published: Oct. 15, 2023
Prostate
cancer
is
the
most
commonly
diagnosed
malignancy
and
sixth
leading
cause
of
death
in
men
worldwide.
Chromosomal
instability
(CIN)
polyploid
giant
cells
(PGCCs)
have
been
considered
predominant
hallmarks
cancer.
Recent
clinical
studies
proven
association
CIN,
aneuploidy,
PGCCs
with
poor
prognosis
prostate
(PCa).
Evidence
HCMV
transforming
potential
might
indicate
that
may
be
involved
PCa.Herein,
we
underline
role
high-risk
HCMV-DB
-BL
strains
epithelial
assess
molecular
cellular
oncogenic
processes
associated
PCa.Oncogenesis
parallels
a
sustained
growth
"CMV-Transformed
cells"
or
CTP
highly
express
Myc
EZH2,
forming
soft
agar
colonies
displaying
stemness
as
well
mesenchymal
features,
hence
promoting
EMT
spheroid
appearance.HCMV-induced
EZH2
upregulation
coupled
traits
IE1-expressing
highlight
PCa
development
encourage
use
anti-EZH2
anti-HCMV
treatment.
Developmental Cell,
Journal Year:
2024,
Volume and Issue:
59(19), P. 2523 - 2531
Published: Oct. 1, 2024
A
paradigm
shift
in
the
study
of
cell
death
is
currently
occurring:
whereas
previously
we
had
always
considered
that
there
were
"points
no
return"
any
pathway,
now
realize
many
types
active,
regulated
death,
this
not
case.
We
are
also
learning
cells
"almost
die,"
but
nevertheless
survive,
can
transiently
take
on
an
altered
state,
with
potential
implications
for
understanding
cancer
therapies
and
relapse.
In
perspective,
parse
forms
by
analogy
to
suicide,
sabotage,
murder,
consider
how
might
be
"instructed"
engage
a
pathway
survive.