Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: March 28, 2023
As
oncogenes
or
tumor
suppressor
genes,
lncRNAs
played
an
important
role
in
tumorigenesis
and
the
progression
of
human
cancers.
The
lncRNA
SNHG15
has
recently
been
revealed
to
be
dysregulated
malignant
tumors,
suggesting
aberrant
expression
which
contributes
clinical
features
regulates
various
oncogenic
processes.
We
have
selected
extensive
literature
focused
on
from
electronic
databases,
including
studies
relevant
its
significance
critical
events
cancer-related
processes
such
as
cell
proliferation,
apoptosis,
autophagy,
metastasis,
drug
resistance.
This
review
summarized
current
understanding
cancer,
mainly
focusing
pathological
features,
known
biological
functions,
underlying
molecular
mechanisms.
Furthermore,
well-documented
effective
diagnostic
prognostic
marker
for
offering
novel
therapeutic
interventions
specific
subsets
cancer
cells.
Briefings in Bioinformatics,
Journal Year:
2021,
Volume and Issue:
23(1)
Published: Nov. 5, 2021
Abstract
Long
non-coding
ribonucleic
acids
(RNAs)
(lncRNAs)
are
key
players
in
tumorigenesis
and
immune
responses.
The
nature
of
their
cell
type-specific
gene
expression
other
functional
evidence
support
the
idea
that
lncRNAs
have
distinct
cellular
functions
tumor
microenvironment
(TIME).
To
date,
majority
lncRNA
studies
heavily
relied
on
bulk
RNA-sequencing
data
which
various
types
contribute
to
an
averaged
signal,
limiting
discovery
functions.
Single-cell
(scRNA-seq)
is
a
potential
solution
for
tackling
this
limitation
despite
lack
annotations
low
abundance
yet
lncRNAs.
Hence,
updated
further
understanding
will
be
necessary
characterizing
genes
TIME.
In
review,
we
discuss
specifically
expressed
cells,
summarize
regulatory
at
type
level
highlight
how
scRNA-seq
approach
can
help
study
TIME
Translational Oncology,
Journal Year:
2023,
Volume and Issue:
39, P. 101821 - 101821
Published: Nov. 4, 2023
Cancer
heterogeneity
and
drug
resistance
remain
pivotal
obstacles
in
effective
cancer
treatment
management.
One
major
contributor
to
these
challenges
is
epigenetic
modifications
-
gene
regulation
that
does
not
involve
changes
the
DNA
sequence
itself
but
significantly
impacts
expression.
As
we
elucidate
phenomena,
underscore
role
of
regulating
expression,
contributing
cellular
diversity,
driving
adaptive
can
instigate
therapeutic
resistance.
This
review
dissects
essential
methylation,
histone
modifications,
chromatin
remodeling
illustrating
their
significant
yet
complex
contributions
biology.
While
offer
potential
avenues
for
intervention
due
reversible
nature,
interplay
genetic
cells
presents
unique
must
be
addressed
harness
full
potential.
By
critically
analyzing
current
research
landscape,
identify
knowledge
gaps
propose
future
directions,
exploring
therapies
discussing
translating
concepts
into
treatments.
comprehensive
aims
stimulate
further
aid
developing
innovative,
patient-centered
therapies.
Understanding
critical
scientific
advancement
paves
way
towards
improving
patient
outcomes
fight
against
this
formidable
disease.
Molecular Cancer,
Journal Year:
2022,
Volume and Issue:
21(1)
Published: Feb. 21, 2022
Abstract
Accumulating
research
suggests
that
the
tumor
immune
microenvironment
(TIME)
plays
an
essential
role
in
regulation
of
growth
and
metastasis.
The
cellular
molecular
nature
TIME
influences
cancer
progression
metastasis
by
altering
ratio
immune-
suppressive
versus
cytotoxic
responses
vicinity
tumor.
Targeting
or
activating
components
show
a
promising
therapeutic
avenue
to
combat
cancer.
success
immunotherapy
is
both
astounding
unsatisfactory
clinic.
Advancements
RNA-based
technology
have
improved
understanding
complexity
diversity
its
effects
on
therapy.
TIME-related
RNA
regulators
could
be
targets
for
anticancer
immunotherapy.
In
this
review,
we
discuss
available
immunotherapies
targeting
TIME.
More
importantly,
summarize
potential
various
therapeutics
clinically
treatment.
RNA-dependent
TIME,
as
monotherapy
combined
with
other
evolving
therapeutics,
might
beneficial
patients’
treatment
near
future.
Non-coding RNA Research,
Journal Year:
2024,
Volume and Issue:
9(3), P. 887 - 900
Published: April 4, 2024
In
the
intricate
field
of
cancer
biology,
researchers
are
increasingly
intrigued
by
emerging
role
exosomal
long
non-coding
RNAs
(lncRNAs)
due
to
their
multifaceted
interactions,
complex
modulation
mechanisms,
and
potential
therapeutic
applications.
These
lncRNAs,
carried
within
extracellular
vesicles,
play
a
vital
partin
tumorigenesis
disease
progression
facilitating
communication
networks
between
tumor
cells
local
microenvironment,
making
them
an
ideal
candidates
for
use
in
liquid
biopsy
approach.
However,
lncRNAs
remain
understudied
area,
especially
biology.
Therefore
this
review
aims
comprehensively
explore
dynamic
interplay
various
cellular
components,
including
interactions
with
tumor-stroma,
immune
modulation,
drug
resistance
mechanisms.
Understanding
regulatory
functions
these
processes
can
potentially
unveil
novel
diagnostic
markers
targets
cancer.
Additionally,
emergence
RNA-based
therapeutics
presents
exciting
opportunities
targeting
offering
innovative
strategies
combat
improve
treatment
outcomes.
Thus,
provides
insights
into
current
understanding
highlighting
crucial
roles,
evolving
landscape
interventions.
Furthermore,
we
have
also
discussed
advantage
exosomes
as
carriers
development
personalized
targeted
therapy
patients.
Frontiers in Molecular Biosciences,
Journal Year:
2022,
Volume and Issue:
9
Published: Feb. 14, 2022
Colon
cancer
(CC)
is
one
of
the
most
frequent
malignancies
in
world,
with
a
high
rate
morbidity
and
death.
In
CC,
necroptosis
long
noncoding
RNA
(lncRNAs)
are
crucial,
but
mechanism
not
completely
clear.
The
goal
this
study
was
to
create
new
signature
that
might
predict
patient
survival
tumor
immunity
patients
CC.
Expression
profiles
necroptosis-related
lncRNAs
473
CC
were
retrieved
from
TCGA
database.
A
consensus
clustering
analysis
based
on
differentially
expressed
(DE)
genes
prognostic
model
least
absolute
shrinkage
selection
operator
(LASSO)
regression
conducted.
Clinicopathological
correlation
analysis,
expression
difference
PCA,
TMB,
GO
KEGG
enrichment
immune
prediction
clinical
therapeutic
compounds,
qRT-PCR
also
Fifty-six
found
be
linked
prognosis,
performed.
There
substantial
variations
survival,
checkpoint
expression,
clinicopathological
correlations,
among
different
subgroups.
Six
discovered,
split
into
high-risk
low-risk
groups
risk
score
generated
using
these
six
lncRNAs.
time
considerably
longer
than
patients,
indicating
directly
associated
survival.
stage,
infiltration
depth,
lymph
node
metastasis,
distant
metastasis.
After
univariate
multivariate
Cox
stage
remained
significant.
Cancer-
metabolism-related
pathways
enriched
by
analyses.
Immune
shown
differ
significantly
between
high-
immunoassay.
Eight
compounds
screened
out,
confirmed
differential
Overall,
have
an
important
function,
prognosis
can
predicted
They
may
useful
future
for
customized
therapy.
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Feb. 9, 2022
Tumorigenesis
is
a
complicated
process
caused
by
successive
genetic
and
epigenetic
alterations.
The
past
decades
demonstrated
that
the
immune
system
affects
tumorigenesis,
tumor
progression,
metastasis.
Although
increasing
immunotherapies
are
revealed,
only
tiny
proportion
of
them
effective.
Long
non-coding
RNAs
(lncRNAs)
class
single-stranded
RNA
molecules
larger
than
200
nucleotides
essential
in
molecular
network
oncology
immunology.
Increasing
researches
have
focused
on
connection
between
lncRNAs
cancer
immunotherapy.
However,
in-depth
mechanisms
still
elusive.
In
this
review,
we
outline
latest
studies
functions
microenvironment.
Via
participating
various
biological
processes
such
as
neutrophil
recruitment,
macrophage
polarization,
NK
cells
cytotoxicity,
T
functions,
regulate
invasion,
epithelial-mesenchymal
transition
(EMT),
angiogenesis.
addition,
reviewed
current
understanding
relevant
strategies
for
targeting
lncRNAs.
LncRNAs-based
therapeutics
may
represent
promising
approaches
serving
prognostic
biomarkers
or
potential
therapeutic
targets
cancer,
providing
ideas
future
research
clinical
application
diagnosis
therapies.
Biomedicines,
Journal Year:
2022,
Volume and Issue:
10(5), P. 1065 - 1065
Published: May 4, 2022
Placenta-specific
trophoblast
and
tumor
cells
exhibit
many
common
characteristics.
Trophoblast
invade
maternal
tissues
while
being
tolerated
by
the
immune
system.
Similarly,
can
surrounding
escape
Importantly,
both
are
supported
an
abetting
microenvironment,
which
influences
invasion,
angiogenesis,
tolerance/evasion,
among
others.
However,
in
contrast
to
cells,
metabolic,
proliferative,
migrative,
invasive
states
of
under
tight
regulatory
control.
In
this
review,
we
provide
overview
similarities
dissimilarities
processes
that
drive
cell
fate,
particularly
focusing
on
role
microenvironments.
Clinical and Translational Medicine,
Journal Year:
2022,
Volume and Issue:
12(6)
Published: June 1, 2022
Obesity
alters
metabolic
microenvironment
and
is
thus
associated
with
several
tumours.
The
aim
of
the
present
study
was
to
investigate
role,
molecular
mechanism
action,
potential
clinical
value
lipid
metabolism-related
long
non-coding
RNA
(lncRNA)
SLC25A21-AS1
in
oesophageal
squamous
cell
carcinoma
(ESCC).A
high-fat
diets
(HFDs)-induced
obesity
nude
mouse
model
established,
targeted
metabolomics
analysis
used
identify
critical
medium-long
chain
fatty
acids
influencing
growth
ESCC
cells.
Transcriptomic
public
dataset
GSE53625
confirmed
that
lncRNA
a
lncRNA.
biological
function
investigated
both
vivo
vitro.
Chromatin
immunoprecipitation(ChIP)assay,
RNA-pull
down,
mass
spectrometry,
co-IP,
IP(RIP)
were
performed
explore
mechanism.
Finally,
an
cDNA
microarray
determine
prognostic
by
RT-qPCR.Palmitic
acid
(PA)
important
component
HFD
had
inhibitory
effect
on
lines.
LncRNA
expression
downregulated
PA
proliferation
migration
cells
vitro
vivo.
Mechanistically,
interacted
nucleophosmin-1
(NPM1)
protein
promote
downstream
gene
transcription
c-Myc
nucleus.
In
cytoplasm,
maintained
stability
SLC25A21
mRNA
reduced
intracellular
NAD+
/NADH
ratio
tryptophan
catabolism.
we
demonstrated
high
promoted
resistance
cisplatin-induced
apoptosis
correlated
poor
tumour
grade
overall
survival.HFD/PA
has
expression.
promotes
regulating
NPM1/c-Myc
axis
addition,
may
serve
as
favourable
biomarker
therapeutic
target
for
ESCC.