Pharmacological Research,
Journal Year:
2024,
Volume and Issue:
206, P. 107280 - 107280
Published: June 22, 2024
Digestive
tract
cancers
are
among
the
most
common
malignancies
worldwide
and
have
high
incidence
mortality
rates.
Thus,
discovery
of
more
effective
diagnostic
therapeutic
targets
is
urgently
required.
The
development
technologies
to
accurately
detect
RNA
modification
has
led
identification
numerous
chemical
modifications
in
humans
(epitranscriptomics)
that
involved
occurrence
digestive
cancers.
can
cooperatively
regulate
gene
expression
facilitate
normal
physiological
functions
system.
However,
dysfunction
relevant
RNA-modifying
enzymes
("writers,"
"erasers,"
"readers")
lead
Consequently,
targeting
dysregulated
enzyme
activity
could
represent
a
potent
strategy
for
treatment
In
this
review,
we
summarize
widely
studied
roles
mechanisms
(m6A,
m1A,
m5C,
m7G,
A-to-I
editing,
pseudouridine
[Ψ])
relation
cancers,
highlight
crosstalk
between
modifications,
discuss
their
interactions
system
microbiota
during
carcinogenesis.
clinical
significance
novel
methods
based
on
also
discussed.
This
review
will
help
guide
future
research
into
resistant
current
therapeutics.
Frontiers in Physiology,
Journal Year:
2023,
Volume and Issue:
14
Published: Aug. 16, 2023
Extracellular
vesicles
(EVs),
including
exosomes,
play
a
crucial
role
in
intercellular
communication
and
have
emerged
as
important
mediators
the
development
progression
of
gastric
cancer.
This
review
discusses
current
understanding
EVs,
particularly
exosomal
lncRNA
microRNA,
cancer
their
potential
diagnostic
therapeutic
targets.
Exosomes
are
small
membrane-bound
particles
secreted
by
both
cells
stromal
within
tumor
microenvironment.
They
contain
various
ncRNA
biomolecules,
which
can
be
transferred
to
recipient
promote
growth
metastasis.
In
this
review,
we
highlighted
importance
microRNA
Exosomal
lncRNAs
been
shown
regulate
gene
expression
interacting
with
transcription
factors
or
chromatin-modifying
enzymes,
binding
target
mRNAs.
We
also
discuss
use
microRNAs
biomarkers
for
isolated
from
bodily
fluids,
blood,
urine,
saliva.
specific
molecules
that
reflect
molecular
characteristics
tumor,
making
them
promising
candidates
non-invasive
tests.
Finally,
targeting
strategy
were
reviewed
wee.
Inhibition
exosomes
has
suppress
metastasis
preclinical
models.
conclusion,
article
provides
an
overview
suggest
further
research
into
these
could
lead
new
tools
strategies
deadly
disease.
Biomedicine & Pharmacotherapy,
Journal Year:
2023,
Volume and Issue:
167, P. 115527 - 115527
Published: Sept. 24, 2023
While
previous
research
on
cancer
biology
has
focused
genes
that
code
for
proteins,
in
recent
years
it
been
discovered
non-coding
RNAs
(ncRNAs)play
key
regulatory
roles
cell
biological
functions.
NcRNAs
account
more
than
95%
of
human
transcripts
and
are
an
important
entry
point
the
study
mechanism
development.
An
increasing
number
studies
have
demonstrated
ncRNAs
can
act
as
tumor
suppressor
or
oncogenes
to
regulate
development
at
epigenetic
level,
transcriptional
well
post-transcriptional
level.
Because
importance
cancer,
most
clinical
trials
explore
whether
be
used
new
biomarkers
therapies.
In
this
review,
we
focus
including
microRNAs
(miRNAs),
long
(lncRNAs),
circle
(circRNAs),
PIWI
interacting
(piRNAs),
tRNA
different
types
application
these
identification
relevant
therapeutic
targets
biomarkers.
Graphical
abstract
drawn
by
Fidraw.
Journal of Cancer,
Journal Year:
2024,
Volume and Issue:
15(9), P. 2845 - 2865
Published: Jan. 1, 2024
Insulin
like
growth
factor
2
mRNA
binding
protein
3
(IGF2BP3)
is
a
critical
m6A
reader.It
encodes
proteins
that
contain
several
KH
domains,
which
are
important
in
RNA
binding,
synthesis
and
metabolism.Lots
of
researches
have
studied
the
malignant
potential
readers
tumors.However,
biological
functional
analysis
IGF2BP3
hepatocellular
carcinoma
(HCC)
pan-cancer
not
comprehensive.In
this
study,
we
used
bioinformatics
approach
to
comprehensively
analyze
significance
HCC
through
analyzing
its
expression,
mutation,
prognosis,
protein-protein
interaction
(PPI)
network,
enrichment,
correlation
with
ferroptosis,
stemness
as
well
immune
modulation
HCC.IGF2BP3
presented
negative
ferroptosis
molecule
NFE2L2,
positive
SLC1A5
checkpoint
HAVCR2.In
addition,
also
analyzed
prognosis
pan-cancer,
revealing
prognostic
value
variety
tumors.Finally,
verified
functions
various
experiments.The
data
showed
may
enhance
proliferation,
colony
formation
invasion
capacities
cells,
mainly
positively
correlated
expression
level
marker
SOX2.In
conclusion,
had
be
new
perspective
biomarker
forecasting
response,
or
even
pan-cancer.
Communications Biology,
Journal Year:
2024,
Volume and Issue:
7(1)
Published: July 2, 2024
Abstract
Gastric
cancer
(GC)
is
the
5
th
most
prevalent
and
4
primary
cancer-associated
mortality
globally.
As
first
identified
m6A
demethylase
for
removing
RNA
methylation
modification,
fat
mass
obesity-associated
protein
(
FTO
)
plays
instrumental
roles
in
development.
Therefore,
we
study
biological
functions
oncogenic
mechanisms
of
GC
tumorigenesis
progression.
In
our
study,
expression
obviously
upregulated
tissues
cells.
The
upregulation
associated
with
advanced
nerve
invasion,
tumor
size,
LNM,
as
well
poor
prognosis
patients,
promoted
cell
viability,
colony
formation,
migration
invasion.
Mechanistically,
targeted
specificity
1
Aurora
Kinase
B,
resulting
phosphorylation
ataxia
telangiectasia
mutated
P38
dephosphorylation
P53.
conclusion,
promotes
progression
by
regulating
SP1-AURKB-ATM
pathway,
which
may
highlight
potential
a
diagnostic
biomarker
patients’
therapy
response
prognosis.
International Journal of Nanomedicine,
Journal Year:
2025,
Volume and Issue:
Volume 20, P. 1597 - 1613
Published: Feb. 1, 2025
Purpose:
Circular
RNAs
(circRNAs)
are
associated
with
the
progression
of
tumors
and
hold
promise
as
potential
biomarkers
for
liquid
biopsy.
Among
these,
role
circPRMT5
in
head
neck
squamous
cell
carcinoma
(HNSCC)
remains
to
be
elucidated.
This
study
aims
examine
underlying
mechanisms
HNSCC
assess
its
diagnostic
value
saliva
exosomes.
Methods:
The
expression
clinical
significance
were
investigated.
Both
vitro
vivo
studies
performed
elucidate
biological
HNSCC.
RNA
sequencing
was
utilized
identify
downstream
mechanisms.
To
evaluate
validate
these
mechanisms,
Western
blotting,
RNA-FISH,
immunofluorescence,
immunohistochemistry,
RIP,
rescue
experiments
employed.
Finally,
salivary
exosomes
isolated,
levels
assessed
using
qRT-PCR.
Results:
upregulation
tissues
identified
correlated
cervical
lymph
node
metastasis
advanced
T
stage.
manifested
that
promoted
proliferation
Mechanistically,
demonstrated
directly
bind
stabilize
insulin-like
growth
factor
2
mRNA-binding
protein
3
(IGF2BP3),
which,
subsequently,
binds
stabilizes
serpin
family
E
member
1
(SERPINE1)
mRNA,
thereby
enhancing
SERPINE1
expression.
Furthermore,
indicated
proliferative,
invasive,
migratory
effects
dependent
on
involvement
IGF2BP3
SERPINE1.
Notably,
significantly
elevated
patients,
exhibiting
substantial
value.
Conclusion:
CircPRMT5
exhibits
significant
utility
through
plays
a
crucial
promoting
via
IGF2BP3-SERPINE1
pathway.
These
findings
highlight
noninvasive
biomarker
therapeutic
target
patients
Keywords:
cancer,
circPRMT5,
IGF2BP3,
SERPINE1,
Molecular Medicine,
Journal Year:
2025,
Volume and Issue:
31(1)
Published: March 25, 2025
Abstract
Background
Chemotherapy
resistance
is
a
major
challenge
in
the
treatment
of
intermediate
and
advanced
gastric
cancer
(GC).
This
study
aimed
to
recognize
oxaliplatin
resistance-related
genes
(OXARGs)
GC
explore
their
role
mechanism
GC.
Methods
OXARGs
with
prognostic
value
were
analyzed
using
data
from
GEO
TCGA
databases.
RT-qPCR
WB
assay
applied
verify
expression
MT2A,
NOTCH1
SLC7A5
oxaliplatin-resistant
cells
(HGC27R
MKN45R).
The
effect
on
malignant
phenotype
was
verified
by
CCK-8,
EDU,
TUNEL,
colony
formation,
wound
healing,
transwell
assay,
tumor
bearing
experiments
assay.
Results
Bioinformatics
analysis
experimental
validation
indicate
that
target
for
oxaliplatin-resistance
Knockdown
obviously
decreased
viability,
migration,
invasion
vitro
growth
vivo.
It
also
increased
apoptosis
levels
BAX
expression,
reduced
BCL2,
MMP
2
MMP9.
Additionally,
knockdown
enhanced
sensitivity
both
Furthermore,
downregulated
HK2,
LDHA,
Glut1,
PDK1
vivo
vitro,
leading
extracellular
glucose
lactate
levels.
However,
glutathione
significantly
attenuated
regulatory
cells.
Trial
registration
Not
Applicable.
Conclusion
inhibits
progression
attenuates
suppressing
glycolysis.
Cancer Drug Resistance,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 28, 2025
Acquired
drug
resistance
is
a
main
factor
contributing
to
cancer
therapy
failure
and
high
mortality,
highlighting
the
necessity
develop
novel
intervention
targets.
Circular
RNAs
(circRNAs),
an
abundant
class
of
RNA
molecules
with
closed
loop
structure,
possess
characteristics
including
stability,
which
provide
unique
advantages
in
clinical
application.
Growing
evidence
indicates
that
aberrantly
expressed
circRNAs
are
associated
against
various
treatments,
targeted
therapy,
chemotherapy,
radiotherapy,
immunotherapy.
Therefore,
targeting
these
aberrant
may
offer
strategy
improve
efficiency
therapy.
Herein,
we
present
summary
most
recently
studied
their
regulatory
roles
on
resistance.
With
advances
artificial
intelligence
(AI)-based
bioinformatics
algorithms,
could
emerge
as
promising
biomarkers
targets