Exosome-based immunotherapy as an innovative therapeutic approach in melanoma
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: Oct. 31, 2024
The
malignant
form
of
melanoma
is
one
the
deadliest
human
cancers
that
accounts
for
almost
all
skin
tumor-related
fatalities
in
its
later
stages.
Achieving
an
exhaustive
understanding
reliable
cancer-specific
markers
and
molecular
pathways
can
provide
numerous
practical
techniques
direct
way
toward
development
rational
curative
medicines
to
increase
lifespan
patients.
Immunotherapy
has
significantly
enhanced
treatment
metastatic
late-stage
melanoma,
resulting
incredible
positive
responses
therapy.
Despite
increasing
occurrence
median
survival
rate
patients
with
advanced,
inoperable
terminal
disease
increased
from
around
six
months
years.
current
knowledge
tumor
microenvironment
(TME)
interaction
immune
system
resulted
swift
growth
innovative
immunotherapy
treatments.
Exosomes
are
small
extracellular
vesicles
(EVs),
ranging
30
150
nm
size,
majority
cells
released
them.
possess
natural
advantages
such
as
high
compatibility
living
organisms
low
potential
causing
reactions,
making
them
delivering
therapeutic
agents
like
chemotherapy
drugs,
nucleic
acids,
proteins.
This
review
highlights
recent
advancements
using
exosomes
approach
providing
medications
melanoma.
Language: Английский
Tenascin-C targeting strategies in cancer
Matrix Biology,
Journal Year:
2024,
Volume and Issue:
130, P. 1 - 19
Published: April 18, 2024
Language: Английский
Primary Cutaneous Melanoma—Management in 2024
Journal of Clinical Medicine,
Journal Year:
2024,
Volume and Issue:
13(6), P. 1607 - 1607
Published: March 11, 2024
Background:
Maximizing
survival
for
patients
with
primary
cutaneous
melanomas
(melanomas)
depends
on
an
early
diagnosis
and
appropriate
management.
Several
new
drugs
have
been
shown
to
improve
in
high-risk
melanoma
patients.
Despite
well-documented
guidelines,
many
do
not
receive
optimal
management,
particularly
when
considering
patient
age.
Objective:
provide
update
management
from
the
time
of
decision
biopsy
a
suspicious
skin
lesion.
Methods:
We
reviewed
melanoma-management
research
published
between
2018
2023
identified
where
such
findings
impact
confirmed
melanomas.
Pubmed,
Google
Scholar,
Ovid
Cochrane
Library
were
used
as
search
tools.
Results:
81
publications
since
2017
that
changed
management;
11
2018,
12
2019,
10
2020,
2021,
17
2022
18
2023.
Discussion:
Delayed
or
inaccurate
is
more
likely
occur
partial
shave
punch
obtain
histopathology.
Wherever
feasible,
local
excision
narrow
margin
should
be
method
choice
suspected
melanoma.
The
Breslow
thickness
remains
single
most
important
predictor
outcome,
followed
by
age
then
ulceration.
BAUSSS
biomarker,
(Breslow
thickness,
Age,
Ulceration,
Subtype,
Sex
Site)
provides
accurate
determining
mortality
risk
than
older
currently
employed
approaches,
including
sentinel
lymph
node
biopsy.
Patients
metastatic
and/or
nodal
disease
considered
adjuvant
drug
therapy
(ADT).
Further,
are
increasingly
ADT,
even
without
spread.
Invasive
less
1
mm
thick
usually
managed
radial
mms
normal
skin.
If
2
mm,
select
20
mm.
When
over
clinical
undertaken.
In
situ
5
Mohs
control
surgery.
Such
wide
excisions
around
given
only
surgery
can
regarded
therapeutic
required.
who
had
one
at
increased
another
Ideal
ongoing
includes
regular
lifelong
checks.
Total
body
photography
if
has
naevi,
especially
atypical/dysplastic
naevi
identified.
Targeted
approaches
occupational
lifestyle
exposure
ultraviolet
light
important.
Management
also
needs
include
consideration
vitamin
D
supplementary
therapy.
Language: Английский
ALDH2 is a novel biomarker and exerts an inhibitory effect on melanoma
Lei Hua,
No information about this author
Jinfeng Liao,
No information about this author
Xinyu Wang
No information about this author
et al.
Scientific Reports,
Journal Year:
2024,
Volume and Issue:
14(1)
Published: Feb. 20, 2024
Abstract
Melanoma
is
a
malignant
skin
tumor.
This
study
aimed
to
explore
and
assess
the
effect
of
novel
biomarkers
on
progression
melanoma.
Differently
expressed
genes
(DEGs)
were
screened
from
GSE3189
GSE46517
datasets
Gene
Expression
Omnibus
database
using
GEO2R.
Ontology
Kyoto
Encyclopedia
Genes
Genomes
pathway
analyses
conducted
based
identified
DEGs.
Hub
assessed
protein–protein
interaction
networks,
principal
component
analysis,
receiver
operating
characteristic
curves.
Quantitative
real-time
polymerase
chain
reaction
was
employed
measure
mRNA
expression
levels.
TIMER
revealed
association
between
aldehyde
dehydrogenase
2
(ALDH2)
tumor
immune
microenvironment.
The
viability,
proliferation,
migration,
invasion
detected
by
cell
counting
kit-8,
5-ethynyl-2′-deoxyuridine,
wound
healing,
transwell
assays.
Total
241
common
DEGs
out
datasets.
We
determined
6
hub
with
high
prediction
values
for
melanoma,
which
could
distinguish
samples
normal
samples.
ALDH2,
ADH1B,
ALDH3A2,
DPT,
EPHX2,
GATM
down-regulated
in
A375
SK-MEL-2
cells,
compared
human
melanin
line
(PIG1
cells).
ALDH2
selected
as
candidate
gene
this
research,
presenting
diagnostic
predictive
value
had
positive
correlation
infiltrating
levels
cells
melanoma
Overexpression
inhibited
A375/SK-MEL-2
cells.
new
biomarker
exerts
an
inhibitory
Language: Английский
YY1-induced lncRNA00511 promotes melanoma progression via the miR-150-5p/ADAM19 axis
Ya-Ni Chen
No information about this author
American Journal of Cancer Research,
Journal Year:
2024,
Volume and Issue:
14(2), P. 809 - 831
Published: Jan. 1, 2024
Increasing
evidence
indicates
that
long
noncoding
RNAs
(lncRNAs)
are
therapeutic
targets
and
key
regulators
of
tumors
development
progression,
including
melanoma.Long
intergenic
non-protein-coding
RNA
511
(LINC00511)
has
been
demonstrated
as
an
oncogenic
molecule
in
breast,
stomach,
colorectal,
lung
cancers.However,
the
precise
role
functional
mechanisms
LINC00511
melanoma
remain
unknown.This
study
confirmed
was
highly
expressed
cells
(A375
SK-Mel-28
cells)
tissues,
knockdown
could
inhibit
cell
migration
invasion,
well
growth
subcutaneous
tumor
xenografts
vivo.By
using
Chromatin
immunoprecipitation
(ChIP)
assay,
it
transcription
factor
Yin
Yang
1
(YY1)
is
capable
binding
to
promoter
enhancing
its
expression
cis.Further
mechanistic
investigation
showed
mainly
enriched
cytoplasm
interacted
directly
with
microRNA-150-5p
(miR-150-5p).Consistently,
miR-150-5p
recover
effects
on
cells.Furthermore,
ADAM
metallopeptidase
domain
19
(ADAM19)
identified
a
downstream
target
miR-150-5p,
overexpression
ADAM19
promote
proliferation.Rescue
assays
indicated
acted
competing
endogenous
(ceRNA)
sponge
increase
ADAM19,
thereby
activating
PI3K/AKT
pathway.In
summary,
we
lncRNA
defined
LINC00511/miR-150-5p/ADAM19
axis,
which
might
be
considered
potential
novel
molecular
mechanism
treatment
patients
melanoma.
Language: Английский
Gasdermin E as a potential target and biomarker for CRISPR-Cas9-based cancer therapy
Biochemical Pharmacology,
Journal Year:
2025,
Volume and Issue:
unknown, P. 116961 - 116961
Published: April 1, 2025
Language: Английский
Unveiling the Dynamic Interplay between Cancer Stem Cells and the Tumor Microenvironment in Melanoma: Implications for Novel Therapeutic Strategies
Cancers,
Journal Year:
2024,
Volume and Issue:
16(16), P. 2861 - 2861
Published: Aug. 16, 2024
Cutaneous
melanoma
still
represents
a
significant
health
burden
worldwide,
being
responsible
for
the
majority
of
skin
cancer
deaths.
Key
advances
in
therapeutic
strategies
have
significantly
improved
patient
outcomes;
however,
most
patients
experience
drug
resistance
and
tumor
relapse.
Cancer
stem
cells
(CSCs)
are
small
subpopulation
different
tumors,
including
melanoma,
endowed
with
distinctive
capacities
self-renewal
differentiation
into
bulk
cells.
Melanoma
CSCs
characterized
by
expression
specific
biomarkers
intracellular
pathways;
moreover,
they
play
pivotal
role
onset,
progression
resistance.
In
recent
years,
great
efforts
been
made
to
dissect
molecular
mechanisms
underlying
protumor
activities
provide
basis
novel
CSC-targeted
therapies.
Herein,
we
highlight
intricate
crosstalk
between
bystander
microenvironment
(TME),
immune
cells,
endothelial
cancer-associated
fibroblasts
(CAFs),
its
progression.
Specifically,
discuss
peculiar
escape
host
surveillance,
recruit
immunosuppressive
educate
toward
an
phenotype.
We
also
address
currently
investigated
that
could
pave
way
new
promising
approaches
care.
Language: Английский
YY1-induced lncRNA00511 promotes melanoma progression via the miR-150- 5p/ADAM19 axis
yani Chen,
No information about this author
Xinrui Fu,
No information about this author
Hua Guo
No information about this author
et al.
Research Square (Research Square),
Journal Year:
2023,
Volume and Issue:
unknown
Published: June 29, 2023
Abstract
Background
Long
noncoding
RNAs
(lncRNAs)
are
key
regulators
of
oncogenic
processes,
and
one
such
lncRNA
is
lncRNA511
(LINC00511),
which
associated
with
breast,
stomach,
lung,
colorectal
cancers.
However,
its
specific
involvement
in
melanoma
remains
unclear.
Here,
we
aimed
to
investigate
the
expression
functional
role
LINC00511
melanoma.
Methods
We
examined
cell
lines
(A375
SK-Mel-28)
tissues
obtained
from
patients.
conducted
knockdown
experiments
assess
effects
on
migration,
invasion,
tumor
growth
in
vivo.
To
transcription
regulators,
performed
chromatin
immunoprecipitation
assays.
Additionally,
analyzed
subcellular
localization
confirmed
that
interaction
microRNA-150-5p
(miR-150-5p)
by
RNA
assay
(RIP),
miRNA
pull-down
luciferase
reporter
assay.
Furthermore,
rescue
assays
validate
our
findings,
namely
LINC00511/miR-150-5p/ADAM19
axis
impact
PI3K/AKT
pathway.
Results
was
found
be
highly
expressed
patient
tissues.
Knockdown
resulted
inhibition
subcutaneous
Yin
Yang
1
(YY1)
identified
as
factor
responsible
for
upregulation.
predominantly
localized
cytoplasm
exhibited
direct
miR-150-5p.
miR-150-5p
rescued
silencing
cells.
Moreover,
ADAM19
a
downstream
target
miR-150-5p,
overexpression
promoted
proliferation.
Rescue
acted
competing
endogenous
RNA,
sponging
increasing
expression,
culminating
activation
Conclusion
This
study
establishes
an
defines
novel
axis,
represents
promising
therapeutic
treatment.
Further
investigations
targeting
this
hold
potential
improving
outcomes
Language: Английский
Comparative genome-wide identification and characterization of SET domain-containing and JmjC domain-containing proteins in piroplasms
Qindong Liang,
No information about this author
Shangdi Zhang,
No information about this author
Zeen Liu
No information about this author
et al.
BMC Genomics,
Journal Year:
2024,
Volume and Issue:
25(1)
Published: Aug. 26, 2024
SET
domain-containing
histone
lysine
methyltransferases
(HKMTs)
and
JmjC
demethylases
(JHDMs)
are
essential
for
maintaining
dynamic
changes
in
methylation
across
parasite
development
infection.
However,
information
on
the
HKMTs
JHDMs
human
pathogenic
piroplasms,
such
as
Babesia
duncani
microti,
veterinary
important
pathogens,
including
bigemina,
bovis,
Theileria
annulata
parva,
is
limited.
A
total
of
38
putative
KMTs
eight
were
identified
using
a
comparative
genomics
approach.
Phylogenetic
analysis
revealed
that
can
be
divided
into
subgroups,
while
belong
to
JARID
subfamily,
except
BdJmjC1
(BdWA1_000016)
TpJmjC1
(Tp
Muguga_02g00471)
which
cluster
with
domain
only
subfamily
members.
The
motifs
domains
highly
conserved
among
piroplasm
species.
Interspecies
collinearity
provided
insight
evolutionary
duplication
events
some
gene
families.
Moreover,
relative
expression
by
RT‒qPCR
demonstrated
KMT
JHDM
families
differentially
expressed
different
intraerythrocytic
developmental
stages
B.
duncani,
suggesting
their
role
Apicomplexa
development.
Our
study
provides
theoretical
foundation
guidance
understanding
basic
characteristics
several
biological
roles
differentiation.
Language: Английский
Advances in Tumor-Infiltrating Lymphocyte (TIL) as a Prognostic Factor and for Treating Invasive Cutaneous Melanoma
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(23), P. 12596 - 12596
Published: Nov. 23, 2024
Invasive
cutaneous
melanoma
is
responsible
for
about
5%
of
skin
tumors
yet
liable
nearly
70%
cancer-related
deaths.
Despite
notable
advancements
over
the
past
decade,
including
immunotherapies
and
targeted
treatments,
more
than
half
invasive
patients
ultimately
succumb
to
disease
due
therapeutic
resistance.
To
overcome
this
obstacle,
strategies
such
as
combining
with
drugs
or
adding
epigenetic
therapies
have
been
investigated.
Tumor-infiltrating
lymphocytes
(TILs)
therapy
has
emerged
a
promising
option
whose
continues
progress
despite
standard
treatments.
This
article
aims
introduce
TIL
review
recent
outcomes
in
prognosis
its
application
management.
Language: Английский