Frontiers in Oncology,
Год журнала:
2021,
Номер
11
Опубликована: Май 31, 2021
Breast
cancer
(BRCA)
is
the
most
leading
cause
of
worldwide.
It
a
heterogeneous
disease
with
at
least
five
molecular
subtypes
including
luminal
A,
B,
basal-like,
HER2-enriched,
and
normal-like.
These
are
usually
stratified
according
to
their
mRNA
profile
patterns;
however,
ncRNAs
increasingly
being
used
for
this
purpose.
Among
class,
long
non-coding
RNAs
(lncRNAs)
molecules
more
than
200
nucleotides
versatile
regulatory
roles;
high
tissue-specific
expression
profiles.
The
heterogeneity
BRCA
can
also
be
reflected
regarding
tumor
microenvironment
immune
cells
composition,
which
directly
impact
patient’s
prognosis
therapy
response.
Using
immunogenomics
data
from
previous
study,
we
propose
here
bioinformatics
approach
include
lncRNAs
complexity
in
subtype.
RNA-seq
Cancer
Genome
Atlas
(TCGA)
cohort
was
analyzed,
signal-to-noise
ratio
metrics
were
applied
create
these
subtype-specific
signatures.
Five
immune-related
signatures
generated
approximately
ten
specific
lncRNAs,
then
functionally
analyzed
using
GSEA
enrichment
survival
analysis.
We
highlighted
some
each
LINC01871
related
response
activation
favorable
overall
basal-like
samples;
EBLN3P
suppression
progression
MEG3,
XXYLT1-AS2,
LINC02613
HER2-enriched
normal-like
subtypes,
respectively.
In
way,
emphasize
need
know
better
role
as
regulators
provide
new
perspectives
diagnosis,
therapeutical
targets
subtypes.
International Journal of Molecular Sciences,
Год журнала:
2023,
Номер
24(17), С. 13617 - 13617
Опубликована: Сен. 3, 2023
Long
non-coding
RNAs
(lncRNAs)
are
crucial
players
in
the
pathogenesis
of
non-small-cell
lung
cancer
(NSCLC).
A
competing
binding
lncRNAs
and
mRNAs
with
microRNAs
(miRNAs)
is
one
most
common
mechanisms
gene
regulation
by
NSCLC,
which
has
been
extensively
researched
last
two
decades.
However,
alternative
that
do
not
depend
on
miRNAs
have
also
reported.
Among
them,
intriguing
mechanism
mediated
RNA-binding
proteins
(RBPs)
such
as
IGF2BP1/2/3,
YTHDF1,
HuR,
FBL,
increase
stability
target
mRNAs.
IGF2BP2
YTHDF1
may
be
involved
m6A
modification
or
Some
lncRNAs,
DLGAP1-AS2,
MALAT1,
MNX1-AS1,
SNHG12,
several
depending
target:
lncRNA/miRNA/mRNA
interactome
through
RBP.
The
protein
sets
selected
here
were
then
analyzed
using
DAVID
database
to
identify
pathways
overrepresented
KEGG,
Wikipathways,
Reactome
pathway.
Using
STRING
website,
we
assessed
interactions
between
built
networks.
Our
analysis
revealed
JAK-STAT
Hippo
signaling
pathways,
cytokine
VEGFA-VEGFR2
pathway,
cell
cycle
regulation,
neovascularization
relevant
effect
lncRNA
NSCLC.
Cancers,
Год журнала:
2019,
Номер
11(11), С. 1802 - 1802
Опубликована: Ноя. 16, 2019
As
a
highly
heterogeneous
malignancy,
breast
cancer
(BC)
has
become
the
most
significant
threat
to
female
health.
Distant
metastasis
and
therapy
resistance
of
BC
are
responsible
for
cases
mortality
recurrence.
relies
on
an
array
processes,
such
as
cell
proliferation,
epithelial-to-mesenchymal
transition
(EMT),
mesenchymal-to-epithelial
(MET),
angiogenesis.
Long
non-coding
RNA
(lncRNA)
refers
class
with
length
over
200
nucleotides.
Currently,
rising
number
studies
have
managed
investigate
association
between
lncRNA.
In
this
study,
we
summarized
how
lncRNA
dual
effects
in
by
regulating
invasion,
migration,
distant
cells.
We
also
emphasize
that
crucial
regulatory
stemness
angiogenesis
BC.
Clinically,
some
lncRNAs
can
regulate
chemotherapy
sensitivity
patients
may
function
novel
biomarkers
diagnose
or
predict
prognosis
patients.
The
exact
impact
clinical
relevance
deserves
further
study.
This
review
be
approach
understanding
BC,
thereby
linking
quasi-personalized
treatment
future.
Cancer Letters,
Год журнала:
2020,
Номер
473, С. 90 - 97
Опубликована: Янв. 2, 2020
Triple
negative
breast
cancer
(TNBC)
is
a
subtype
which
particularly
aggressive
and
invasive.
The
treatment
of
TNBC
has
been
limited
due
to
the
lack
well-defined
molecular
targets.
Exosomes
are
nano-sized
extracellular
vesicles
that
released
from
virtually
all
cell
types
into
space.
Due
their
endocytic
origin,
exosomes
carry
valuable
information
cells
origin.
were
first
thought
serve
as
"garbage
disposals"
eliminate
unwanted
cellular
components.
Later,
they
found
be
involved
in
pathology
many
diseases
including
cancer.
Despite
established
roles
multiple
diseases,
only
small
number
studies
have
focused
on
role
TNBC.
In
this
review,
we
outline
progression,
metastasis
drug
resistance
subtype.
We
then
further
illustrate
potential
diagnostic
tools,
therapeutic
targets
delivery
systems.
Cancer Cell International,
Год журнала:
2020,
Номер
20(1)
Опубликована: Янв. 10, 2020
Melanoma
is
the
most
aggressive
type
of
skin
cancer
with
high
mortality
rate
and
poor
prognosis.
lncRNA
MEG3,
a
tumor
suppressor,
closely
related
to
development
various
cancers.
However,
role
MEG3
in
melanoma
has
seldom
been
studied.RT-PCR
was
used
examine
expressions
E-cadherin
patients
cell
lines.
Then,
biological
functions
were
demonstrated
by
transfecting
MEG3-siRNA,
MEG3-overexpression,
E-cadherin-siRNA
E-cadherin-overexpression
plasmids
Moreover,
CCK8
assay
colony
formation
utilized
assess
proliferation;
Transwell
performed
evaluate
invasive
ability;
xenografts
nude
mice
applied
test
generation.
Additionally,
target
interactions
among
miR-21
determined
dual
luciferase
reporter
assay.
Finally,
RT-PCR
WB
further
conducted
verify
regulatory
roles
E-cadherin.The
clinical
data
showed
that
both
declined
carcinoma
tissues
as
compared
their
para-carcinoma
tissues.
B16
cells
also
higher
than
those
A375
A2058
cells.
Subsequently,
based
on
differently
expressed
these
human
lines,
we
chose
B16,
for
following
experiments.
The
results
could
suppress
growth,
metastasis
formation;
meanwhile
had
same
effects
formation.
Furthermore,
analysis
Kaplan-Meier
curves
confirmed
there
positive
correlation
between
E-cadherin.
Ultimately,
assays
directly
which
turn.
revealed
knockdown
inhibited
expression
promoted
expression,
but
overexpression
presented
completely
opposite
results.Our
findings
indicated
might
inhibit
modulating
miR-21/E-cadherin
axis.
Neuro-Oncology,
Год журнала:
2020,
Номер
22(12), С. 1771 - 1784
Опубликована: Май 21, 2020
Glioblastoma
(GBM)
stemlike
cells
(GSCs)
are
thought
to
be
responsible
for
the
maintenance
and
aggressiveness
of
GBM,
most
common
primary
brain
tumor
in
adults.
This
study
aims
at
elucidating
involvement
deregulations
within
imprinted
delta-like
homolog
1
gene‒type
III
iodothyronine
deiodinase
gene
(DLK-DIO3)
region
on
chromosome
14q32
GBM
pathogenesis.Real-time
PCR
analyses
were
performed
GSCs
tissues.
Methylation
analyses,
expression,
reverse-phase
protein
array
profiles
used
investigate
suppressor
function
maternally
expressed
3
(MEG3).Loss
expression
genes
noncoding
RNAs
DLK1-DIO3
was
observed
tissues
compared
with
normal
brain.
downregulation
is
mainly
mediated
by
epigenetic
silencing.
Kaplan-Meier
analysis
indicated
that
low
MEG3
MEG8
long
(lnc)RNAs
significantly
correlated
short
survival
patients.
restoration
impairs
tumorigenic
abilities
vitro
inhibiting
cell
growth,
migration,
colony
formation
decreases
vivo
reducing
infiltrative
growth.
These
effects
associated
modulation
involved
adhesion
epithelial-to-mesenchymal
transition
(EMT).In
acts
as
a
regulating
adhesion,
EMT,
proliferation,
thus
providing
potential
candidate
novel
therapies.
Frontiers in Oncology,
Год журнала:
2021,
Номер
11
Опубликована: Июль 12, 2021
Glioma
is
the
most
common
malignant
central
nervous
system
tumor
with
significant
mortality
and
morbidity.
Despite
considerable
advances,
exact
molecular
pathways
involved
in
progression
are
not
fully
elucidated,
patients
commonly
face
a
poor
prognosis.
Long
non-coding
RNAs
(lncRNAs)
have
recently
drawn
extra
attention
for
their
potential
roles
different
types
of
cancer
as
well
non-malignant
diseases.
More
than
200
lncRNAs
been
reported
to
be
associated
glioma.
We
aimed
assess
investigated
stages
mediating
addition
clinical
applications.
formation,
invasion,
progression,
including
regulating
cell
cycle,
apoptosis,
autophagy,
epithelial-to-mesenchymal
transition,
stemness,
angiogenesis,
integrity
blood-tumor-brain
barrier,
metabolism,
immunological
responses.
The
well-known
oncogenic
lncRNAs,
which
upregulated
glioma,
H19
,
HOTAIR
PVT1
UCA1
XIST
CRNDE
FOXD2-AS1
ANRIL
HOXA11-AS
TP73-AS1
DANCR
.
On
other
hand,
MEG3
GAS5
CCASC2
TUSC7
suppressor
downregulated.
While
studies
effects
MALAT1
TUG1
NEAT1
there
some
controversies
regarding
these
lncRNAs.
Expression
levels
can
grade,
survival,
treatment
response
(chemotherapy
drugs
or
radiotherapy),
overall
Moreover,
circulatory
such
MALAT1,
H19,
HOTAIR,
NEAT1,
TUG1,
GAS5,
LINK-A
provide
non-invasive
diagnostic
prognostic
tools.
Modulation
expression
using
antisense
oligonucleotides
lead
novel
therapeutics.
Notably,
profound
understanding
underlying
function
required
develop
therapeutic
targets.
investigations
large
sample
sizes
increased
focus
on
in-vivo
models
expand
our
application
Cell Death and Disease,
Год журнала:
2021,
Номер
13(1)
Опубликована: Дек. 21, 2021
Abstract
Background
Colorectal
cancer
(CRC)
remains
the
most
common
gastrointestinal
and
a
leading
cause
of
deaths
worldwide,
with
showing
pathologies
indicating
malignant
transformation
early
stage
intestinal
stem
cells.
The
long
non-coding
RNA
Meg3
,
which
functions
as
tumor
suppressor,
has
been
reported
to
be
abnormal
in
multiple
tumorigenesis
events;
however,
underlying
mechanism
by
contributes
proliferation
colonic
cells
unclear.
Methods
We
analyzed
expression
levels
miR-708
SOCS3
samples
from
Apc
loss-of-function
(
min
)
mice
patients
CRC,
particularly
crypt
AMO/DSS-induced
model
(in
vivo)
organoid
culture
system
vitro)
were
used
explore
effect
/
/SOCS3
axis
on
colon.
In
vitro,
we
performed
RNApull-down,
immunoprecipitation,
luciferase
reporter
assays
using
DLD1
RKO
cell
lines.
Findings
signaling
plays
critical
role
CRC
development.
Our
data
showed
negatively
correlate
both
clinical
mouse
model,
indicated
that
acts
competitive
endogenous
(ceRNA)
.
Then,
served
an
oncogene,
inducing
neoplasia
cultured
organoids.
Put
together,
appears
promote
targeting
SOCS3/STAT3
signaling.
Interpretation
These
revealed
sponges
inhibit
development
via
SOCS3-mediated
repression
provides
potential
targets
for
diagnosis
treatment
CRC.
Drug Design Development and Therapy,
Год журнала:
2024,
Номер
Volume 18, С. 1385 - 1398
Опубликована: Апрель 1, 2024
In
the
past
few
decades,
chemotherapy
has
been
one
of
most
effective
cancer
treatment
options.
Drug
resistance
is
currently
greatest
obstacles
to
treatment.
Even
though
drug
mechanisms
have
extensively
investigated,
they
not
fully
elucidated.
Recent
genome-wide
investigations
revealed
existence
a
substantial
quantity
long
non-coding
RNAs
(lncRNAs)
transcribed
from
human
genome,
which
actively
participate
in
numerous
biological
processes,
such
as
transcription,
splicing,
epigenetics,
cell
cycle,
differentiation,
development,
pluripotency,
immune
microenvironment.
The
abnormal
expression
lncRNA
considered
contributing
factor
resistance.
Furthermore,
may
be
influenced
by
genetic
and
epigenetic
variations,
well
individual
differences
patient
response,
attributable
polymorphisms
metabolic
enzyme
genes.
This
review
focuses
on
mechanism
lncRNAs
target
drugs
study
tumors
with
high
mortality,
aiming
establish
theoretical
foundation
for
targeted
therapy.