Frontiers in Bioscience-Landmark,
Journal Year:
2025,
Volume and Issue:
30(1)
Published: Jan. 17, 2025
Since
the
discovery
of
Musashi
(MSI)
protein,
its
ability
to
affect
mitosis
Drosophila
progenitor
cells
has
garnered
significant
interest
among
scientists.
In
following
20
years,
it
lived
up
expectations.
A
substantial
body
evidence
demonstrated
that
is
closely
related
development,
metastasis,
migration,
and
drug
resistance
malignant
tumors.
recent
research
on
MSI
protein
advanced,
many
novel
viewpoints
attempts
have
been
derived;
for
example,
tumor
p53
mutations
MSI-binding
proteins
lead
arginine
N-methyltransferase
5-targeted
therapy
in
lymphoma
patients.
Moreover,
high
expression
MSI2
pancreatic
cancer
might
suppress
development
progression.
As
a
member
family,
associated
with
multiple
tumors,
including
hematological
disorders,
common
abdominal
other
types
(e.g.,
glioblastoma,
breast
cancer).
highly
expressed
majority
tumors
poor
disease
prognosis.
However,
specific
levels
regulatory
mechanisms
may
differ
based
type.
This
review
summarizes
progress
occurrence,
migration
mechanism,
resistance,
as
well
prospect
developing
immunosuppressants
biomarkers.
Frontiers in Oncology,
Journal Year:
2022,
Volume and Issue:
12
Published: Aug. 17, 2022
Cancer
is
one
of
the
most
frequently
diagnosed
malignant
diseases
worldwide,
posing
a
serious,
long-term
threat
to
patients’
health
and
life.
Systemic
chemotherapy
remains
first-line
therapeutic
approach
for
recurrent
or
metastatic
cancer
patients
after
surgery,
with
potential
effectively
extend
patient
survival.
However,
development
drug
resistance
seriously
limits
clinical
efficiency
ultimately
results
in
treatment
failure
death.
A
large
number
studies
have
shown
that
non-coding
RNAs
(ncRNAs),
particularly
microRNAs,
long
RNAs,
circular
are
widely
involved
regulation
resistance.
Their
dysregulation
contributes
by
modulating
expression
specific
target
genes
cellular
apoptosis,
autophagy,
efflux,
epithelial-to-mesenchymal
transition
(EMT),
stem
cells
(CSCs).
Moreover,
some
ncRNAs
also
possess
great
as
efficient,
biomarkers
diagnosis
prognosis
well
targets
patients.
In
this
review,
we
summarize
recent
findings
on
emerging
role
underlying
mechanisms
focus
their
applications
treatment.
This
information
will
be
benefit
early
prognostic
assessments
ncRNA-based
strategies
Molecular Cancer,
Journal Year:
2024,
Volume and Issue:
23(1)
Published: Aug. 30, 2024
Drug
resistance
in
cancer
cells
significantly
diminishes
treatment
efficacy,
leading
to
recurrence
and
metastasis.
A
critical
factor
contributing
this
is
the
epigenetic
alteration
of
gene
expression
via
RNA
modifications,
such
as
N6-methyladenosine
(m6A),
N1-methyladenosine
(m1A),
5-methylcytosine
(m5C),
7-methylguanosine
(m7G),
pseudouridine
(Ψ),
adenosine-to-inosine
(A-to-I)
editing.
These
modifications
are
pivotal
regulating
splicing,
translation,
transport,
degradation,
stability.
Governed
by
"writers,"
"readers,"
"erasers,"
impact
numerous
biological
processes
progression,
including
cell
proliferation,
stemness,
autophagy,
invasion,
apoptosis.
Aberrant
can
lead
drug
adverse
outcomes
various
cancers.
Thus,
targeting
modification
regulators
offers
a
promising
strategy
for
overcoming
enhancing
efficacy.
This
review
consolidates
recent
research
on
role
prevalent
resistance,
with
focus
m6A,
m1A,
m5C,
m7G,
Ψ,
A-to-I
Additionally,
it
examines
regulatory
mechanisms
linked
underscores
existing
limitations
field.
Acta Pharmaceutica Sinica B,
Journal Year:
2022,
Volume and Issue:
13(3), P. 982 - 997
Published: Oct. 7, 2022
Chemotherapy
is
one
of
the
important
methods
to
treat
cancer,
and
emergence
multidrug
resistance
(MDR)
major
cause
for
failure
cancer
chemotherapy.
Almost
all
anti-tumor
drugs
develop
drug
over
a
period
time
application
in
patients,
reducing
their
effects
on
killing
cells.
Chemoresistance
can
lead
rapid
recurrence
cancers
ultimately
patient
death.
MDR
may
be
induced
by
multiple
mechanisms,
which
are
associated
with
complex
process
genes,
factors,
pathways,
steps,
today
MDR-associated
mechanisms
largely
unknown.
In
this
paper,
from
aspects
protein–protein
interactions,
alternative
splicing
(AS)
pre-mRNA,
non-coding
RNA
(ncRNA)
mediation,
genome
mutations,
variance
cell
functions,
influence
tumor
microenvironment,
we
summarize
molecular
cancers.
end,
prospects
exploration
antitumor
that
reverse
briefly
discussed
angle
systems
improved
targeting
properties,
biocompatibility,
availability,
other
advantages.
Biomarker Research,
Journal Year:
2023,
Volume and Issue:
11(1)
Published: Jan. 4, 2023
Metastasis
is
a
significant
factor
that
affects
the
survival
of
patients
with
non-small
cell
lung
cancer
(NSCLC).
Nevertheless,
molecular
regulatory
mechanism
underlying
metastasis
currently
not
fully
understood.
This
study
aims
to
identify
important
role
miR-124-3p
in
NSCLC,
thereby
providing
potential
therapeutic
intervention.Exosome
secretion
was
determined
by
Nanoparticle
Tracking
Analysis
(NTA)
and
uptake
measured
fluorescence
inverted
microscope.
The
binding
between
its
upstream
or
downstream
target
genes
validated
experimentally
Luciferase
reporter.
Cells
migration
evaluated
transwell
assays.
Transcriptome
sequencing
on
A549
carried
out
verify
signaling
pathway
regulation.
Western
blotting
analysis
used
assess
level
AKT,
p-AKT,
PI3K,
p-PI3K
protein
expression
NSCLC
lines.
suppress
tumor
verified
xenograft
model.Exosomes
were
more
abundant
serum
from
advanced
(n
=
24
patients)
than
these
early-stage
30
patients),
which
suggested
correlation
amount
exosome
NSCLC.
Interestingly,
release,
cells
notably
inhibited
miR-124-3p.
LINC00511
suppressed
facilitate
transport
due
as
competitive
endogenous
RNA
for
could
directly
3'-UTR
Rab27a
inhibit
prevent
invasion.
Aside
inhibition
transport,
activation
PI3K/AKT
intracellular
environment.
Finally,
measuring
subcutaneous
weight
volume
metastasis,
we
also
demonstrated
growth
vivo.In
significantly
through
extracellular
signaling.
These
findings
provide
new
insights
toward
better
understanding
suggest
treatment
biomarker
Signal Transduction and Targeted Therapy,
Journal Year:
2023,
Volume and Issue:
8(1)
Published: Oct. 27, 2023
Abstract
Cardiovascular
disease
(CVD)
is
the
leading
cause
of
death
in
world,
with
a
high
incidence
and
youth-oriented
tendency.
RNA
modification
ubiquitous
indispensable
cell,
maintaining
cell
homeostasis
function
by
dynamically
regulating
gene
expression.
Accumulating
evidence
has
revealed
role
aberrant
expression
CVD
caused
dysregulated
modification.
In
this
review,
we
focus
on
nine
common
modifications:
N
6
-methyladenosine
(m
A),
1
5-methylcytosine
5
C),
7
-methylguanosine
G),
4
-acetylcytosine
(ac
pseudouridine
(Ψ),
uridylation,
adenosine-to-inosine
(A-to-I)
editing,
modifications
U34
tRNA
wobble.
We
summarize
key
regulators
their
effects
expression,
such
as
splicing,
maturation,
transport,
stability,
translation.
Then,
based
classification
CVD,
mechanisms
which
occurs
progresses
through
are
discussed.
Potential
therapeutic
strategies,
therapy,
reviewed
these
mechanisms.
Herein,
some
(such
stroke
peripheral
vascular
disease)
not
included
due
to
limited
availability
literature.
Finally,
prospective
applications
challenges
discussed
for
purpose
facilitating
clinical
Moreover,
look
forward
more
studies
exploring
roles
future,
there
substantial
uncultivated
areas
be
explored.
Journal of Experimental & Clinical Cancer Research,
Journal Year:
2023,
Volume and Issue:
42(1)
Published: Dec. 18, 2023
Abstract
Background
Research
has
indicated
that
long-term
sleep
deprivation
can
lead
to
immune
dysfunction
and
participate
in
the
occurance
progression
of
tumors.
However,
relationship
between
colon
cancer
remains
unclear.
This
study
explored
specific
mechanism
through
which
promotes
proliferation
migration
cancer,
with
a
focus
on
neurotransmitter
GABA.
Methods
Chronic
mice
model
were
used
investigate
effect
disorder
We
detected
levels
peripheral
blood
using
ELISA.
CCK-8
assay,
colony
formation
wound
healing
transwell
assay
performed
GABA
cells,
while
immunofluorescence
showed
distribution
macrophages
lung
metastatic
tissues.
isolated
exosomes
from
GABA-induced
culture
medium
explore
effects
cells
macrophages.
Gain-
loss-of-function
experiments,
luciferase
report
analysis,
immunohistochemistry,
cytokine
detection
reveal
crosstalk
Results
Sleep
promote
level
cell
migration.
Immunofluorescence
analysis
revealed
metastasis
is
associated
enhanced
recruitment
lungs.
The
co-culture
results
intensified
M2
polarization
macrophage
induced
by
cells.
due
activation
MAPK
pathway
tumor-derived
exosomal
miR-223-3p.
Furthermore,
M2-like
tumor
secreting
IL-17.
also
identified
an
endogenous
miR-223-3p
downregulation
E3
ligase
CBLB,
enhances
stability
cMYC
protein
augments
ability.
Notably,
acts
as
transcription
factor
regulate
expression
Conclusion
Our
suggest
GABA,
leading
CBLB
inhibition
ubiquitination.
Simultaneously,
extracellular
polarization,
leads
secretion
IL-17,
further
enhancing
Pharmacological Research - Modern Chinese Medicine,
Journal Year:
2024,
Volume and Issue:
10, P. 100386 - 100386
Published: Feb. 4, 2024
The
most
significant
obstacle
in
addressing
cancer
is
the
development
of
multidrug
resistance
during
chemotherapy.
Cancer
cells
have
ability
to
endure
numerous
cycles
traditional
chemotherapy
drugs
before
ultimately
developing
treatment.
Combining
a
strategy
used
address
problem
resistance.
Persistent
challenges
with
synthetic
include
catastrophic
adverse
reactions
and
other
consequences.
Natural
compounds
originating
from
Chinese
medicine
are
acknowledged
for
their
minimal
toxicity
possible
benefits
reversing
induced
by
mainstream
chemotherapeutic
or
targeted
treatments.
(MDR)
an
immediate
clinical
justification
unsatisfactory
recurrence
metastasis
precipitated
MDR,
leading
high
risk
death.
unique
nano-delivery
method
therapeutic
management
MDR
cancers
has
emerged
as
key
use
nanotechnology.
Because
its
anticancer
prospective,
(TCM)-combination
therapy
emerging
treatment
modality
essential
option
cancer.
By
precisely
regulating
release
medicines
delivering
pharmaceuticals
cancerous
cells,
nano
drug-delivery
devices
offer
amazing
pave
way
growth
TCM-combination
therapies.
present
review
examines
literature
on
three
important
topics:
mechanism
chemotherapy,
role
herbs
formulation
treatment,
incorporation
TCM
nanotechnology-based
drug
delivery
systems
circumvent
limitations
system.
Major
sources
work
PubMed,
Google
Scholar,
ResearchGate,
Embase,
ScienceDirect.
All
aspects
pertaining
TCM,
nanotechnology
more
than
50
years
were
considered,
emphasis
formulation,
various
forms
advances
system
result
nanotechnology,
everything
else
between.
As
becomes
closely
associated
realm
practice
broadening.
Furthermore,
it
enhances
prospects
future
research
facilitates
advancement
modern
Traditional
Medicine
(TCM).
integrating
into
meticulously
designed
system,
will
enhance
both
treat
prevent
diseases
even
greater
efficacy
previously.
This
article
nano-TCM
explores
characteristics,
compositions,
relevant
techniques
preparation
application
MDR.
In
addition,
comprehensive
elucidation
had
been
given
respect
objective
this
study
was
analyze
existing
body
(TCM)
that
can
be
encompasses
like
active
components
utilization
(MDR),
potential
advancements
obstacles
TCM-based
combinations.
Abstract
Hepatocellular
carcinoma
(HCC)
is
a
common
malignant
tumor
with
high
recurrence
rate
and
poor
prognosis.
Long
intergenic
nonprotein
coding
RNA
942
(LINC00942)
reported
to
be
related
ferroptosis
the
immune
response
in
HCC
serves
as
an
oncogene
various
cancers.
This
research
aimed
explore
contribution
of
LINC00942
progression.
Functional
assays
were
used
evaluate
functional
role
vitro
vivo.
Mechanistic
conducted
assess
association
insulin-like
growth
factor
2
mRNA
binding
protein
3
(IGF2BP3)
solute
carrier
family
7
member
11
(SLC7A11)
regulatory
pattern
cells.
was
found
exhibit
upregulation
tissue
facilitated
cell
proliferation,
suppressed
ferroptosis,
converted
naive
CD4
+
T
cells
inducible
Treg
(iTreg)
by
regulating
SLC7A11.
Furthermore,
SLC7A11
expression
positively
modulated
IGF2BP3
shared
RNA-binding
(RBP)
for
The
between
3′
untranslated
region
verified,
recruit
promote
stability
m6A-dependent
manner.
Moreover,
mouse
proliferation
inhibited,
number
FOXP3
CD25
increased,
while
enhanced
after
knockdown
suppresses
induces
immunosuppression
recruiting
enhance
stability,
which
may
provide
novel
therapeutic
targets
HCC.