Oncology Letters,
Год журнала:
2017,
Номер
unknown
Опубликована: Дек. 5, 2017
The
long
non‑coding
RNA,
FAM83H
antisense
RNA
1
(head
to
head)
(FAM83H‑AS1),
has
exhibited
a
functional
role
as
an
oncogene
in
number
of
different
types
cancer.
aim
the
present
study
was
reveal
dysregulation
FAM83H‑AS1
colorectal
carcinoma
(CRC)
samples
and
elucidate
its
underlying
associations
with
Notch
signaling
pathway.
expression
profiles
two
signaling‑associated
molecules,
Notch1
Hes
family
basic‑helix‑loop‑helix
transcription
factor
(Hes1),
were
measured
by
reverse
transcription‑polymerase
chain
reaction
western
blot
analysis.
Pearson
χ2
test
employed
evaluate
between
clinical
features.
A
statistically
significant
positive
association
levels
those
or
Hes1
CRC
tissues
analyzed
Spearman's
correlation
Kaplan‑Meier
method
used
compare
overall
survival
curves
highly‑expressed
low‑expressed
groups
via
log‑rank
test.
Specific
small
hairpin
transfected
silence
endogenous
FAM83H‑AS1.
MTT
colony
formation
assays
performed
measure
growth‑inhibition
effect
silenced
FAM83H‑AS1,
significantly
increased
cell
lines.
Cell
proliferation
markedly
inhibited
when
knocked
down
this
mediated
could
be
reversed
regulators.
Thus,
downregulated
anti‑proliferative
repressing
Glioma
is
one
of
the
most
prevalent
types
primary
intracranial
carcinoma
with
varying
malignancy
grades
I–IV
and
histological
subtypes,
including
astrocytomas,
glioblastoma
multiform
(GBM),
oligodendrogliomas
mixed
tumors.
characterized
by
rapid
cell
proliferation
angiogenesis,
WHO
grade
IV
glioblastoma,
which
highly
malignant
poor
prognosis
because
GBM
stem-like
cells
(GSCs)
are
resistant
to
conventional
therapy
easily
recrudescent,
accounts
for
majority
gliomas.
Consequently,
investigations
exploring
accurate
molecular
mechanisms
reliable
therapeutic
targets
gliomas
have
drawn
extensive
attention.
Based
on
increasing
amount
functional
lncRNAs
aberrantly
expressed
in
glioma
tissues
lines,
might
be
critical
initiation,
progression
other
phenotypes.
This
review
summarizes
latest
insights
into
lncRNA
field
their
roles
glioma,
therefore
evaluating
potential
clinical
applications
as
prospective
novel
biomarkers
targets.
Frontiers in Cell and Developmental Biology,
Год журнала:
2021,
Номер
9
Опубликована: Июнь 10, 2021
Long
non-coding
RNAs
(lncRNAs)
regulate
gene
expression
in
a
variety
of
ways
at
epigenetic,
chromatin
remodeling,
transcriptional,
and
translational
levels.
Accumulating
evidence
suggests
that
lncRNA
X-inactive
specific
transcript
(lncRNA
Xist)
serves
as
an
important
regulator
cell
growth
development.
Despites
its
original
roles
X-chromosome
dosage
compensation,
Xist
also
participates
the
development
tumor
other
human
diseases
by
functioning
competing
endogenous
RNA
(ceRNA).
In
this
review,
we
comprehensively
summarized
recent
progress
understanding
cellular
functions
mammalian
cells
discussed
current
knowledge
regarding
ceRNA
network
various
diseases.
are
transcripts
more
than
200
nt
length
without
apparent
protein-coding
capacity
(Furlan
Rougeulle,
2016;
Maduro
et
al.,
2016).
These
believed
to
be
transcribed
approximately
98-99%
regions
genome
(Derrien
2012;
Fu,
2014;
Montalbano
2017;
Slack
Chinnaiyan,
2019),
well
large
genomic
regions,
such
exonic,
tronic,
intergenic
regions.
Hence,
lncRNAs
divided
into
eight
categories:
Intergenic
lncRNAs,
Intronic
Enhancer
Promoter
Natural
antisense/sense
Small
nucleolar
RNA-ended
(sno-lncRNAs),
Bidirectional
non-poly(A)
(Ma
2013;
Devaux
2015;
St
Laurent
Chen,
Quinn
Chang,
Richard
Eichhorn,
2018;
Connerty
2020).
A
range
has
suggested
function
key
regulators
crucial
functions,
including
proliferation,
differentiation,
apoptosis,
migration,
invasion,
regulating
level
target
genes
via
epigenomic,
or
post-transcriptional
approaches
(Cao
2018).
Moreover,
detected
body
fluids
were
serve
potential
biomarkers
for
diagnosis,
prognosis,
monitoring
disease
progression,
act
novel
drug
targets
therapeutic
exploitation
(Jiang
W.
Zhou
2019a).
set
15,000-20,000
sequences
localized
X
chromosome
inactivation
center
(XIC)
Xq13.2
(Brown
1992;
Debrand
1998;
Kay,
Lee
da
Rocha
Heard,
Yang
Z.
Brockdorff,
2019).
Previous
studies
have
indicated
(XCI),
resulting
inheritable
silencing
one
X-chromosomes
during
female
Also,
it
vital
regulatory
whole
spectrum
(notably
cancer)
can
used
diagnostic
prognostic
biomarker
clinic
(Liu
2018b;
Deng
2019;
Dinescu
Mutzel
Schulz,
2020;
Patrat
Wang
2020a).
particular,
been
demonstrated
involved
multiple
types
tumors
brain
tumor,
Leukemia,
lung
cancer,
breast
liver
with
prominent
examples
outlined
Table
1.
It
was
(Chaligne
2018)
contributed
diseases,
pulmonary
fibrosis,
inflammation,
neuropathic
pain,
cardiomyocyte
hypertrophy,
osteoarthritis
chondrocytes,
details
found
2.
This
review
summarizes
on
mechanisms
both
compensation
pathogenesis
(especially
processes,
focus
disease.
Theranostics,
Год журнала:
2018,
Номер
8(13), С. 3654 - 3675
Опубликована: Янв. 1, 2018
Long
noncoding
RNAs
(lncRNAs)
represent
a
large
subgroup
of
that
are
longer
than
200
nucleotides
and
have
no
apparent
protein
coding
potential.They
diverse
functions
in
different
biological
processes
by
regulating
chromatin
remodeling
or
translation.This
review
summarizes
the
recent
progress
lncRNAs
angiogenesis
vascular
diseases.A
general
overview
lncRNA
functional
mechanisms
will
be
introduced.A
list
lncRNAs,
which
termed
"Angio-LncRs",
including
MALAT1,
MANTIS,
PUNISHER,
MEG3,
MIAT,
SENCR
GATA6-AS,
discussed
regarding
their
expression,
regulation,
function
mechanism
action
angiogenesis.Implications
diseases,
such
as
atherosclerosis,
hypertension,
retinopathies
tumor
also
discussed.
Cancers,
Год журнала:
2018,
Номер
11(1), С. 17 - 17
Опубликована: Дек. 22, 2018
Glioma
is
the
most
aggressive
brain
tumor
of
central
nervous
system.
The
ability
glioma
cells
to
migrate,
rapidly
diffuse
and
invade
normal
adjacent
tissue,
their
sustained
proliferation,
heterogeneity
contribute
an
overall
survival
approximately
15
months
for
patients
with
high
grade
glioma.
Numerous
studies
indicate
that
non-coding
RNA
species
have
critical
functions
across
biological
processes
regulate
initiation
progression.
Recently,
new
data
emerged,
which
shows
cross-regulation
between
long
RNAs
small
phenotypic
diversity
glioblastoma
subclasses.
In
this
paper,
we
review
expression,
was
evaluated
in
human
tissue
samples
during
a
five-year
period.
Thus,
summarizes
following:
(I)
role
pathogenesis,
(II)
potential
application
glioma-grading,
(III)
crosstalk
lncRNAs
miRNAs
(IV)
future
perspectives
as
biomarkers
International Journal of Molecular Sciences,
Год журнала:
2020,
Номер
21(6), С. 1950 - 1950
Опубликована: Март 12, 2020
Glioblastoma
(GBM)
consists
of
a
heterogeneous
collection
competing
cellular
clones
which
communicate
with
each
other
and
the
tumor
microenvironment
(TME).
MicroRNAs
(miRNAs)
present
various
exchange
mechanisms:
free
miRNA,
extracellular
vesicles
(EVs),
or
gap
junctions
(GJs).
GBM
cells
transfer
miR-4519
miR-5096
to
astrocytes
through
GJs.
Oligodendrocytes
located
in
invasion
front
high
levels
miR-219-5p,
miR-219-2-3p,
miR-338-3p,
all
related
their
differentiation.
There
is
reciprocal
between
endothelial
(ECs)
as
promotes
angiogenesis
after
being
transferred
into
ECs,
whereas
miR-145-5p
acts
suppressor.
In
glioma
stem
(GSCs),
miR-1587
miR-3620-5p
increase
proliferation
inhibits
hormone
receptor
co-repressor-1
(NCOR1)
EVs
transfers.
GBM-derived
carry
miR-21
miR-451
that
are
up-taken
by
microglia
monocytes/macrophages,
promoting
proliferation.
Macrophages
release
enriched
cells.
This
bidirectional
increases
STAT3
activity
macrophages,
invasion,
proliferation,
angiogenesis,
resistance
treatment.
miR-1238
upregulated
resistant
EVs,
conferring
adjacent
via
CAV1/EGFR
signaling
pathway.
Decrypting
these
mechanisms
could
lead
better
patient
stratification
development
novel
target
therapies.
Molecular Therapy — Nucleic Acids,
Год журнала:
2021,
Номер
24, С. 728 - 742
Опубликована: Апрель 2, 2021
Glioblastoma
multiforme
(GBM)
is
the
most
widespread
and
aggressive
subtype
of
glioma
in
adult
patients.
Numerous
long
non-coding
RNAs
(lncRNAs)
are
deregulated
or
differentially
expressed
GBM.
These
lncRNAs
possess
unique
regulatory
functions
GBM
cells,
ranging
from
high
invasion/migration
to
recurrence.
This
review
outlines
present
status
specific
involvement
pathogenesis,
with
a
focus
on
their
association
key
molecular
cellular
mechanisms.
Also,
we
highlighted
potential
different
novel
RNA-based
strategies
that
may
be
beneficial
for
therapeutic
purposes.
International Journal of Biological Sciences,
Год журнала:
2021,
Номер
17(3), С. 712 - 727
Опубликована: Янв. 1, 2021
Tight
junction
(TJ)
is
a
"zippering
up"
structure
located
at
the
uppermost
portion
of
adjacent
epithelial/endothelial
cells
in
organs
and
tissues.TJs
maintain
relative
stability
intracellular
substances
functions
by
closing
or
opening
intercellular
pathways,
coordinating
entry
exit
molecules
different
sizes
charges,
regulating
permeability
paracellular
barrier.TJs
also
prevent
microbial
invasion,
cell
polarity,
regulate
proliferation.TJs
are
widely
present
skin
mucosal
epithelial
barriers,
intestinal
barrier,
glomerular
filtration
bladder
blood-brain
brain-blood
tumor
blood-testis
barrier.TJ
dysfunction
can
lead
to
variety
diseases.In
addition
signal
transcription
factors,
DNA
methylation,
histone
modification,
TJ
proteins
be
regulated
non-coding
RNAs,
such
as
micro-RNAs,
long-noncoding
circular
directly
indirectly.This
review
summarizes
TJs
introduces
regulatory
mechanisms
tissues.The
roles
RNAs
regulation
highlighted
this
review.