IGF2BP3 Triggers STAT3 Pathway by Stabilizing SRC RNA in an m6A‐Dependent Manner to Promote Lymphatic Metastasis in LUAD
Jiapei Ding,
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Xuequan Wang,
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Haihua Yang
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et al.
Cancer Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 13, 2025
ABSTRACT
Lymph
node
metastasis
significantly
affects
the
NSCLC
patients'
staging,
treatment
strategy,
and
prognosis.
Studies
have
shown
that
IGF2BP3,
an
oncofetal
protein
m6A
reader,
overexpresses
correlates
to
lymph
worse
overall
survival
in
histopathological
studies
including
NSCLC,
but
its
mechanism
needs
further
study.
This
study
explored
IGF2BP3's
function
LUAD
lymphatic
using
public
databases,
a
human
tissue
microarray,
cells,
model
male
BALB/c
nude
mice.
Firstly,
we
proved
IGF2BP3
overexpression
was
positively
correlated
bioinformatics
microarray
analysis.
knocked
out
or
overexpressed
cell
lines.
Functionally,
facilitated
NCI‐H1299,
NCI‐H358,
A549
growth,
migration,
invasion,
EMT
vitro,
promoted
tumorigenesis,
lymphangiogenesis,
of
NCI‐H1299
cells
Mechanically,
RIP,
RNA
pull‐down
assay,
MeRIP,
mRNA
stability
assays,
rescue
experiments,
immunohistochemical
assays
were
conducted.
demonstrated
bind
site
3′UTR
region
SRC,
stabilizing
activating
downstream
STAT3
signaling
pathway
growth
factors
such
as
VEGF‐C,
therefore
affecting
metastasis.
The
migration
partially
rescued
by
utilizing
SRC
siRNA
AZD0530,
inhibitor.
promotes
via
m6A‐SRC‐STAT3‐VEGFC
axis,
indicating
is
potential
therapeutic
target
overcome
patients.
Language: Английский
CAF-derived exosome-miR-3124-5p promotes malignant biological processes in NSCLC via the TOLLIP/TLR4-MyD88-NF-κB pathway
Tao Sun,
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Qinghua Song,
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Hua Liu
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et al.
Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics,
Journal Year:
2024,
Volume and Issue:
33(1), P. 133 - 148
Published: Sept. 13, 2024
Lung
cancer
is
a
life-threatening
disease
that
occurs
worldwide,
but
especially
common
in
China.
The
crucial
role
of
the
tumour
microenvironment
(TME)
non-small
cell
lung
(NSCLC)
has
attracted
recent
attention.
Cancer-associated
fibroblasts
(CAFs)
are
main
factors
contribute
to
TME
function,
and
CAF
exosomes
closely
linked
NSCLC.
expression
levels
miR-3124-5p
Toll-interacting
protein
(TOLLIP)
were
analysed
by
bioinformatics
prediction
combined
with
RT-qPCR/Western
Blot
detection.
Fibroblasts
isolated
identified
from
clinical
NSCLC
tissues.
Transmission
electron
microscopy
Western
used
identify
these
cells.
Changes
proliferation
(CCK-8
clone
formation),
migration
(wound
healing),
invasion
(transwell)
cells
measured.
Luciferase
reporter
test
was
applied
clarify
binding
TOLLIP.
TOLLIP/TLR4/MyD88/NF-κB
pathway
proteins
determined
using
blot
analysis.
MiR-3124-5p
overexpressed
tissues
dramatically
enriched
CAF-derived
exosomes.
Cellular
experiments
revealed
CAFs
delivered
into
via
exosomes,
stimulating
progression.
acted
as
sponge
negatively
regulate
TOLLIP
expression,
which
activated
TLR4/MyD88/NF-κB
axis
promote
occurrence
development
Functional
salvage
tests
performed
determine
whether
CAF-exosome-derived
plays
pro-cancer
affecting
signalling
pathway.
These
results
provide
an
interesting
direction
for
diagnosis
therapy
Language: Английский
Impact of Nanoparticle Properties on Immune Cell Interactions in the Lymph Node
Acta Biomaterialia,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 1, 2024
Language: Английский
[Predictive Value of A miRNA Signature for Distant Metastasis in Lung Cancer].
PubMed,
Journal Year:
2024,
Volume and Issue:
27(12), P. 919 - 930
Published: Dec. 20, 2024
Lung
cancer
represents
the
main
cause
of
cancer-related
deaths
worldwide,
and
non-small
cell
lung
(NSCLC)
is
most
subtype.
More
than
half
NSCLC
patients
have
already
developed
distant
metastasis
(DM)
at
time
diagnosis
a
poor
prognosis.
Therefore,
it
necessary
to
find
new
biomarkers
for
predicting
DM
in
order
guide
subsequent
treatment
thus
improve
prognosis
patients.
Numerous
studies
shown
that
microRNAs
(miRNAs)
are
abnormally
expressed
tissues
play
an
important
role
tumorigenesis
progression.
The
aim
this
study
identify
differentially
miRNAs
adenocarcinoma
with
group
compared
those
non-distant
(NDM)
group,
construct
miRNA
signature
adenocarcinoma.
We
first
obtained
clinical
data
from
Cancer
Genome
Atlas
(TCGA)
database.
Subsequently,
bioinformatics
analysis,
which
included
different
R
packages,
Kaplan-Meier
receiver
operating
characteristic
(ROC)
curve,
range
online
analysis
tools,
was
performed
analyze
data.
A
total
12
were
identified
between
NDM
groups,
8
(miR-377-5p,
miR-381-5p,
miR-490-5p,
miR-519d-5p,
miR-3136-5p,
miR-320e,
miR-2355-5p,
miR-6784-5p)
screened
constructing
signature.
efficacy
good
area
under
curve
(AUC)
0.831.
Logistic
regression
showed
independent
risk
factor
Next,
target
genes
eight
predicted,
enrichment
these
enriched
variety
pathways,
including
pathways
cancer,
herpes
simplex
virus
I
infection,
PI3K-Akt
pathway,
MAPK
Ras
etc.
CONCLUSIONS:
This
has
potential
be
predictor
Language: Английский