Oncogenic mechanisms of COL10A1 in cancer and clinical challenges (Review)
Oncology Reports,
Год журнала:
2024,
Номер
52(6)
Опубликована: Окт. 8, 2024
Collagen
type
X
α1
chain
(COL10A1),
a
gene
encoding
the
α‑1
of
collagen,
serves
key
role
in
conferring
tensile
strength
and
structural
integrity
to
tissues.
Upregulation
COL10A1
expression
has
been
observed
different
malignancies,
including
lung,
gastric
pancreatic
cancer,
is
associated
with
poor
prognosis.
The
present
review
provides
an
updated
synthesis
evolving
biological
understanding
COL10A1,
particular
focus
on
its
mechanisms
action
regulatory
functions
within
context
tumorigenesis.
For
example,
it
established
that
increased
promotes
cancer
progression
by
activating
multiple
signaling
pathways,
TGF‑β1/Smad,
MEK/ERK
focal
adhesion
kinase
thereby
inducing
proliferation,
invasion
migration.
Additionally,
demonstrated
induce
epithelial‑mesenchymal
transition
reshapes
extracellular
matrix
tumor
Furthermore,
basis
methyltransferase‑like
3‑mediated
N6‑methyladenosine
methylation,
intricately
regulates
epitranscriptomic
machinery,
augmenting
oncogenic
role.
However,
although
pivotal
transcription
orchestration
growth,
question
whether
would
serve
as
viable
therapeutic
target
remains
subject
scientific
hypothesis
requiring
rigorous
examination.
Variables
such
distinct
microenvironments
treatment
associations
necessitate
further
experimental
validation.
Therefore,
comprehensive
assessment
functional
mechanistic
roles
may
pave
way
for
development
innovative
strategies.
Язык: Английский
Pan-cancer analysis reveals MTTP as a prognostic and immunotherapeutic biomarker in human tumors
Frontiers in Immunology,
Год журнала:
2025,
Номер
16
Опубликована: Март 27, 2025
Introduction
Microsomal
triglyceride
transfer
protein
(MTTP)
is
an
essential
lipid
for
the
synthesis
and
secretion
of
very
low
density
lipoprotein
(VLDL)
in
hepatocytes
chylomicrons
(CM)
intestinal
cells.
Further
researches
have
revealed
that
MTTP
exerted
its
functions
a
variety
tissues
beyond
liver
intestine,
including
heart,
neural
antigen-presenting
Dysregulation
expression
can
lead
to
many
diseases,
such
as
metabolism
disorders,
insulin
resistance
cardiovascular
diseases.
Despite
importance,
research
on
cancer
limited,
with
no
comprehensive
pan-cancer
studies
available.
Methods
was
explored
TIMER
2.0
Sangerbox
databases.
The
pathological
stages
survival
analysis
were
analyzed
via
GEPIA
Kaplan
Meier
plotter.
gene
mutations
by
cBioPortal
database.
immune
landscape
tumor
microenvironment(TME)
using
single-cell
sequencing.
Based
RNA-seq
data
TCGA,
we
constructed
GSEA
enrichment
MTTP.
We
identified
pro-tumor
anti-ferroptosis
gastric
(GC)
cells
vitro
vivo
experiments,
effect
TME
ferroptosis
Results
elevated
at
least
1/3
tumors.
High
associated
poor
prognosis
most
levels
significantly
correlated
three
scores
(immune,
stromal,
extimate)
checkpoints
half
types.
Single
cell
sequencing
showed
mainly
expressed
macrophages,
especially
microglia.
increased
GC
knockdown
limited
proliferation,
migration
invasion
abilities
cells,
accompanied
sensitivity
ferroptosis.
In
addition,
analyzing
genes
single
level,
found
macrophages
may
be
involved
process
GC.
Conclusions
Our
study
emphasizes
promising
prognostic
immunotherapeutic
biomarker
infiltration
diverse
regulates
providing
potential
target
immunotherapy.
Язык: Английский
P4HB, a novel succinated protein, is essential for fumarate-induced cancer metastasis
International Journal of Biological Macromolecules,
Год журнала:
2025,
Номер
unknown, С. 143885 - 143885
Опубликована: Май 1, 2025
Язык: Английский
Molecular signatures of disulfidptosis: interplay with programmed cell death pathways and therapeutic implications in oncology
Cellular & Molecular Biology Letters,
Год журнала:
2025,
Номер
30(1)
Опубликована: Июнь 2, 2025
Disulfidptosis
represents
a
newly
identified
form
of
regulated
cell
death
(RCD)
distinct
from
other
well-established
RCD
pathways.
It
occurs
during
periods
glucose
starvation,
specifically
when
intracellular
NADPH
is
rapidly
depleted
and
the
expression
Solute
Carrier
Family
7
Member
11
(SLC7A11)
highly
upregulated.
Cancer
cells
utilize
SLC7A11
to
import
cystine
extracellular
environment,
subsequently
employ
convert
it
into
cysteine.
In
event
deficiency
or
an
impairment
in
its
utilization,
accumulates
within
cells.
This
accumulation
results
abnormal
disulfide
bond
formation
actin
cytoskeleton
proteins,
which
turn
causes
collapse
network
ultimately
triggers
disulfidptosis.
process
uncovers
metabolic
vulnerability
tumors,
offering
novel
perspectives
on
mechanisms
that
underlie
death.
this
paper,
we
provide
comprehensive
review
mechanism
disulfidptosis
compare
similarities
differences
with
common
programmed
mechanisms,
such
as
apoptosis,
autophagy,
ferroptosis,
cuproptosis.
The
aim
gain
more
profound
understanding
characteristics
various
Understanding
correlation
between
tumors
constitutes
crucial
theoretical
foundation
for
future
research
endeavors
cancer
treatment.
offers
valuable
insights
could
pave
way
developing
treatment
strategies
lead
groundbreaking
advancements
therapy.
Язык: Английский
P4HB maintains Wnt-dependent stemness in glioblastoma stem cells as a precision therapeutic target and serum marker
Oncogenesis,
Год журнала:
2024,
Номер
13(1)
Опубликована: Ноя. 23, 2024
Glioblastoma
stem
cells
(GSCs)
are
pivotal
in
the
recurrence
and
drug
resistance
of
glioblastoma
multiforme
(GBM).
However,
precision
therapeutic
diagnostic
markers
for
GSCs
have
not
been
fully
established.
Here,
using
bioinformatics
experimental
analysis,
we
identified
P4HB,
a
protein
disulfide
isomerase,
as
serum
marker
that
maintains
stemness
through
Wnt/β-catenin
signaling
pathway.
Transcriptional
silencing
P4HB
induces
apoptosis
diminishes
cell-like
characteristics
GSCs.
Treatments
with
chemical
CCF624
or
China
National
Medical
Products
Administration
(NMPA)-approved
securinine
significantly
prolonged
survival
patient-derived
xenograft
mouse
models,
underscoring
P4HB's
potential
target
presenting
an
expedited
path
to
clinical
application
repurposing.
Additionally,
elevated
levels
patient
were
found
correlate
disease
progression,
its
utility
biomarker
promise
medicine.
Язык: Английский
Exploring the role of ADAMTSL2 across multiple cancer types: A pan-cancer analysis and validated in colorectal cancer
Qing-xin Yu,
Ruicheng Wu,
Jie Wang
и другие.
Discover Oncology,
Год журнала:
2024,
Номер
15(1)
Опубликована: Окт. 9, 2024
Recent
studies
have
established
a
correlation
between
ADAMTSL2
(ADAMTS-like
2)
and
the
development
of
various
cancers.
This
study
aims
to
conduct
comprehensive
pan-cancer
analysis
in
37
cancer
types
investigate
its
potential
role
colon
rectal
adenocarcinoma
(COADREAD).
Язык: Английский