Aging,
Journal Year:
2020,
Volume and Issue:
13(2), P. 2198 - 2211
Published: Dec. 9, 2020
Circular
RNAs
(circRNAs)
are
associated
with
chemoresistance
in
many
cancers.
However,
the
function
of
circ_0005198
temozolomide
(TMZ)
resistance
glioma
has
not
been
well
elucidated.
Here,
we
demonstrated
that
was
considerably
up-regulated
tissues,
serum
samples
and
TMZ-resistant
cells.
Silencing
restrained
TMZ
resistance,
restricted
proliferation
facilitated
apoptosis
MiR-198
could
be
sponged
by
circ_0005198,
effect
on
progression
cells
attributed
to
inhibition
miR-198
activity.
Moreover,
TRIM14
a
target
silencing
hindered
suppressed
cells,
while
over-expression
rescued
inhibiting
over-expression.
We
conclude
circ_0005198-miR-198-TRIM14
regulatory
pathway
is
critical
glioma.
Journal of Cardiovascular Development and Disease,
Journal Year:
2019,
Volume and Issue:
6(2), P. 15 - 15
Published: April 1, 2019
Cardiovascular
development
is
a
complex
developmental
process
starting
with
the
formation
of
an
early
straight
heart
tube,
followed
by
rightward
looping
and
configuration
atrial
ventricular
chambers.
The
subsequent
step
allows
separation
these
cardiac
chambers
leading
to
four-chambered
organ.
Impairment
in
any
processes
invariably
leads
defects.
Importantly,
our
understanding
defects
causing
congenital
diseases
has
largely
increased
over
last
decades.
advent
molecular
era
allowed
bridge
morphogenetic
genetic
therefore
current
transcriptional
regulation
morphogenesis
enormously
increased.
Moreover,
impact
environmental
agents
cascades
been
demonstrated
as
well
novel
genomic
mechanisms
modulating
gene
such
post-transcriptional
regulatory
mechanisms.
Among
mechanisms,
non-coding
RNAs,
including
therein
microRNAs
lncRNAs,
are
emerging
play
pivotal
roles.
In
this
review,
we
summarize
knowledge
on
functional
role
RNAs
distinct
diseases,
particular
emphasis
long
RNAs.
Cell Death and Disease,
Journal Year:
2020,
Volume and Issue:
11(10)
Published: Oct. 22, 2020
Glioblastoma
(GBM)
is
a
highly
aggressive
tumor
with
poor
prognosis.
A
small
subpopulation
of
glioma
stem
cells
(GSCs)
has
been
implicated
in
radiation
resistance
and
recurrence.
In
this
study
we
analyzed
the
expression
miRNAs
associated
functions
GSCs
using
miRNA
microarray
analysis
these
compared
human
neural
cells.
These
analyses
identified
gene
clusters
cell
invasiveness,
axonal
guidance,
TGF-β
signaling.
miR-504
was
significantly
downregulated
NSCs,
its
lower
GBM
normal
brain
specimens
further
decreased
mesenchymal
subtype.
Overexpression
inhibited
their
self-renewal,
migration
markers.
The
inhibitory
effect
mediated
by
targeting
Grb10
which
acts
as
an
oncogene
GBM.
exogenous
resulted
also
delivery
to
cocultured
microglia
GSC-secreted
extracellular
vesicles
(EVs)
abrogation
GSC-induced
polarization
M2
Finally,
overexpression
prolonged
survival
mice
harboring
GSC-derived
xenografts
growth.
summary,
potential
target
networks
that
play
role
stemness
transition
miR-504/Grb10
pathway
important
regulator
process.
exerted
antitumor
effects
well
bystander
on
via
EVs.
Journal of Cellular and Molecular Medicine,
Journal Year:
2020,
Volume and Issue:
24(11), P. 6362 - 6372
Published: April 22, 2020
Abstract
Glioblastoma
(GBM)
belongs
to
the
high‐grade
(IV)
gliomas
with
extremely
poor
prognosis.
Accumulating
evidence
uncovered
key
roles
of
long
non‐coding
RNAs
(lncRNAs)
in
GBM
development.
This
study
aimed
determine
biological
actions
and
clinical
relevance
lncRNA
MIR4435‐2
Host
Gene
(MIR4435‐2HG)
GBM.
Data
from
GEPIA
database
showed
that
MIR4435‐2HG
was
up‐regulated
tissues
high
expression
correlated
shorter
overall
survival
patients.
Further
experimental
assays
verified
up‐regulation
cell
lines.
In
vitro
studies
vivo
animal
knockdown
resulted
inhibition
proliferation
invasion
tumour
growth,
while
overexpression
driven
progression.
Furthermore,
MIR44435‐2HG
found
sponge
miR‐1224‐5p
suppress
expression;
attenuated
enhancement
induced
by
overexpression.
a
subsequent
study,
target
transforming
growth
factor‐beta
receptor
type
2
(TGFBR2)
repressed
TGFBR2
expression,
exerted
tumour‐suppressive
effects
via
targeting
TGFBR2.
More
importantly,
TGFRB2
antagonized
hyper‐proliferation
cells
Clinically,
down‐regulation
were
samples.
Taken
together,
present
suggests
oncogenic
role
underlies
function
MIR4435‐2HG‐driven
progression
miR‐1224‐5p/TGFBR2
axis.
Aging,
Journal Year:
2020,
Volume and Issue:
12(20), P. 20285 - 20307
Published: Oct. 21, 2020
Glioma
is
one
of
the
most
commonly
diagnosed
brain
malignancies
with
a
high
cancer-related
death
rate
in
humans.
The
prognosis
glioma
patients
still
unsatisfactory.
In
present
study,
we
attempted
to
identify
lncRNAs
and
miRNAs
that
might
be
related
NF-κB-mediated
epithelial-mesenchymal
transition
cells
based
on
online
microarray
expression
profiles,
investigate
specific
effects
lncRNA-miRNA-mRNA
axes
cell
phenotypes.
Herein,
identified
lncRNA
DGCR5
as
downregulated
was
negatively
regulated
by
NF-κB1
an
RE-dependent
manner.
LncRNA
overexpression
significantly
inhibited
capacity
proliferate,
migrate,
invade,
whereas
promoted
apoptosis
cells.
Moreover,
upregulated
epithelial
marker
E-cadherin
while
downregulating
mesenchymal
VIM,
well
Snai2
TWIST.
Regarding
underlying
molecular
mechanisms,
could
inhibit
miR-21
miR-23a
expression,
or
reversed
tumor-suppressive
overexpression.
exerted
its
through
DGCR5/miR-21/Smad7
DGCR5/miR-23a/PTEN
axes.
conclusion,
suppresses
migrate
invade
via
miR-21/Smad7,
it
inhibits
proliferation
enhances
miR-23a/PTEN.
Aging,
Journal Year:
2020,
Volume and Issue:
13(2), P. 2198 - 2211
Published: Dec. 9, 2020
Circular
RNAs
(circRNAs)
are
associated
with
chemoresistance
in
many
cancers.
However,
the
function
of
circ_0005198
temozolomide
(TMZ)
resistance
glioma
has
not
been
well
elucidated.
Here,
we
demonstrated
that
was
considerably
up-regulated
tissues,
serum
samples
and
TMZ-resistant
cells.
Silencing
restrained
TMZ
resistance,
restricted
proliferation
facilitated
apoptosis
MiR-198
could
be
sponged
by
circ_0005198,
effect
on
progression
cells
attributed
to
inhibition
miR-198
activity.
Moreover,
TRIM14
a
target
silencing
hindered
suppressed
cells,
while
over-expression
rescued
inhibiting
over-expression.
We
conclude
circ_0005198-miR-198-TRIM14
regulatory
pathway
is
critical
glioma.