Cell Death Discovery,
Journal Year:
2023,
Volume and Issue:
9(1)
Published: March 25, 2023
Abstract
The
oncogene
MYC
is
dysregulated
in
a
host
of
human
cancers,
and
as
an
important
point
convergence
multitudinous
oncogenic
signaling
pathways,
it
plays
crucial
role
tumor
immune
regulation
the
microenvironment
(TIME).
Specifically,
promotes
expression
immunosuppressive
factors
inhibits
activation
regulators.
Undoubtedly,
therapeutic
strategy
that
targets
can
initiate
new
era
cancer
treatment.
In
this
review,
we
summarize
essential
pathway
immunity
development
status
MYC-related
therapies,
including
strategies
targeting
combined
MYC-based
immunotherapy.
These
studies
have
reported
extraordinary
insights
into
translational
application
treatment
are
conducive
to
emergence
more
effective
immunotherapies
for
cancer.
Journal of Cancer Research and Clinical Oncology,
Journal Year:
2024,
Volume and Issue:
150(1)
Published: Jan. 1, 2024
Abstract
Purpose
This
article
summarizes
natural
products
that
target
the
MAPK-signaling
pathway
in
cancer
therapy.
The
classification,
chemical
structures,
and
anti-cancer
mechanisms
of
these
are
elucidated,
comprehensive
information
is
provided
on
their
potential
use
Methods
Using
PubMed
database,
we
searched
for
keywords,
including
“tumor”,
“cancer”,
“natural
product”,
“phytochemistry”,
“plant
components”,
“MAPK-signaling
pathway”.
We
also
screened
compounds
with
well-defined
structures
targeting
have
effects.
used
Kingdraw
software
Adobe
Photoshop
to
draw
compound
structural
diagrams.
Results
A
total
131
papers
were
searched,
from
which
85
selected.
These
clear
treatment
mainly
related
pathway.
Examples
include
eupatilin,
carvacrol,
oridonin,
sophoridine,
diosgenin,
juglone.
components
classified
as
flavonoids,
phenols,
terpenoids,
alkaloids,
steroidal
saponins,
quinones.
Conclusions
Certain
MAPK
inhibitors
been
clinical
treatment.
However,
feedback
has
not
promising
because
genomic
instability,
drug
resistance,
side
Natural
few
effects,
good
medicinal
efficacy,
a
wide
range
sources,
individual
heterogeneity
biological
activity,
capable
treating
disease
multiple
targets.
characteristics
make
drugs
Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: March 12, 2024
The
breast
cancer
tumor
microenvironment
(TME)
is
dynamic,
with
various
immune
and
non-immune
cells
interacting
to
regulate
progression
anti-tumor
immunity.
It
now
evident
that
the
within
TME
significantly
contribute
resistance
conventional
newly
developed
therapies.
Both
in
play
critical
roles
onset,
uncontrolled
proliferation,
metastasis,
evasion,
Consequently,
molecular
cellular
components
of
have
emerged
as
promising
therapeutic
targets
for
developing
novel
treatments.
primarily
comprises
cells,
stromal
vasculature,
infiltrating
cells.
Currently,
numerous
clinical
trials
targeting
specific
are
underway.
However,
complexity
its
impact
on
evasion
immunity
necessitate
further
research
develop
improved
multifaceted
nature
arises
from
their
phenotypic
functional
plasticity,
which
endows
them
both
pro
during
progression.
In
this
review,
we
discuss
current
understanding
recent
advances
anti-tumoral
functions
implications
safe
effective
therapies
control
progress.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 17, 2025
Breast
cancer
is
the
most
common
malignant
tumor
in
world,
and
its
metastasis
main
cause
of
death
breast
patients.
However,
differences
between
primary
tissue
lymphatic
node,
bone,
brain
metastases
at
single-cell
level
are
not
fully
understood.
We
analyzed
microenvironment
heterogeneity
samples
(n
=
4),
node
3),
bone
2)
using
sequencing
data
from
GEO
database.
The
epithelial
cells
were
characterized
by
InferCNV
algorithm.
cell-cell
communication
was
CellChat
package.
biological
function
cell
subpopulations
gene
set
variation
analysis.
expression
STMN1
immunohistochemical
staining.
proportion
pCAFs
explored
multispectral
identified
seven
clusters
metastatic
(Lymphatic
brain,
metastases)
analyzing
transcriptomic
profiles.
T-NK
B
dominated
with
metastasis,
whereas
fibroblasts
prevalent
cancer.
five
T
(T
memory,
CD8
+
cells,
regulatory
natural
killer
CD4
cells),
three
(naïve
memory
plasma
cancer-associated
(CAFs)
(Smooth
muscle
(SMC),
pericyte,
antigen-presenting
CAFs
(apCAFs),
proliferative
(pCAFs),
matrix
(mCAFs)).
Notably.
metastasis.
Furthermore,
we
four
subpopulations:
G0,
G1,
G2,
G3.
G2
population
exhibited
strong
invasion
ability,
it
can
differentiate
into
G3
ability
proliferation-related
G1
after
Cell-cell
demonstrated
an
interaction
metastasis-associated
cells.
Finally,
discovered
that
advanced
cancer,
pCAF
increased
associated
a
poor
prognosis
This
study
elucidated
potential
cellular
origins
drivers
to
nodes,
utilizing
prognosis.
Stem Cell Research & Therapy,
Journal Year:
2021,
Volume and Issue:
12(1)
Published: April 16, 2021
Abstract
Breast
cancer
is
the
second
common
and
leading
cause
of
malignancy
among
females
overall.
stem
cells
(BCSCs)
are
a
small
population
breast
that
play
critical
role
in
metastasis
to
other
organs
body.
BCSCs
have
both
self-renewal
differentiation
capacities,
which
thought
contribute
aggressiveness
metastatic
lesions.
Therefore,
targeting
can
be
suitable
approach
for
treatment
cancer.
Growing
evidence
has
indicated
Wnt,
NFκB,
Notch,
BMP2,
STAT3,
hedgehog
(Hh)
signaling
pathways
govern
epithelial-to-mesenchymal
transition
(EMT)
activation,
growth,
tumorigenesis
primary
regions.
miRNAs
as
central
regulatory
molecules
also
roles
BCSC
self-renewal,
metastasis,
drug
resistance.
Hence,
these
might
novel
therapeutic
diagnosis
therapy.
This
review
discusses
known
mechanisms
involved
stimulation
or
prevention
tumorigenesis.
Cancers,
Journal Year:
2021,
Volume and Issue:
13(14), P. 3427 - 3427
Published: July 8, 2021
Breast
cancer
is
the
most
frequently
diagnosed
and
leading
cause
of
death
among
women
worldwide.
Despite
overall
successes
in
breast
therapy,
hormone-independent
HER2
negative
cancer,
also
known
as
triple
(TNBC),
lacking
estrogens
progesterone
receptors
with
an
excessive
expression
human
epidermal
growth
factor
receptor
2
(HER2),
along
positive
subtype,
still
remain
major
challenges
treatment.
Due
to
their
poor
prognoses,
aggressive
phenotype,
highly
metastasis
features,
new
alternative
therapies
have
become
urgent
clinical
need.
One
noteworthy
phytochemicals,
curcumin,
has
attracted
enormous
attention
a
promising
drug
candidate
prevention
treatment
due
its
multi-targeting
effect.
Curcumin
interrupts
stages
tumorigenesis
including
cell
proliferation,
survival,
angiogenesis,
through
modulation
multiple
signaling
pathways.
The
current
review
highlighted
anticancer
activity
curcumin
via
focusing
on
impact
key
pathways
PI3K/Akt/mTOR
pathway,
JAK/STAT
MAPK
NF-ĸB
p53
Wnt/β-catenin,
well
apoptotic
cycle
Besides,
therapeutic
implications
trials
are
here
presented.
Cancer Cell International,
Journal Year:
2021,
Volume and Issue:
21(1)
Published: Aug. 10, 2021
Abstract
Triple-negative
breast
cancer
(TNBC)
is
not
as
prevalent
hormone
receptor
or
HER2-positive
cancers
and
all
tests
come
back
negative.
More
importantly,
the
heterogeneity
complexity
of
TNBC
on
molecular
clinical
levels
have
limited
successful
development
novel
therapeutic
strategies
led
to
intrinsic
developed
resistance
chemotherapies
new
agents.
Studies
demonstrated
deregulation
Wnt/β-catenin
signaling
in
tumorigenesis
which
plays
decisive
roles
at
low
survival
rate
patients
facilitates
currently
existing
therapies.
This
review
summarizes
mechanisms
for
TNBC,
complex
interaction
between
signaling,
transactivated
tyrosine
kinase
(RTK)
pathways,
lymphocytic
infiltration,
epithelial-mesenchymal
transition
(EMT),
induction
metastasis.
Such
associations
how
these
pathways
interact
progression
careful
analysis
effective
combination
therapies
without
generating
significant
toxicity
resistance.
Bioinformatics,
Journal Year:
2022,
Volume and Issue:
38(19), P. 4522 - 4529
Published: Aug. 12, 2022
Single-cell
RNA
sequencing
(scRNA-seq)
data
provides
unprecedented
opportunities
to
reconstruct
gene
regulatory
networks
(GRNs)
at
fine-grained
resolution.
Numerous
unsupervised
or
self-supervised
models
have
been
proposed
infer
GRN
from
bulk
RNA-seq
data,
but
few
of
them
are
appropriate
for
scRNA-seq
under
the
circumstance
low
signal-to-noise
ratio
and
dropout.
Fortunately,
surging
TF-DNA
binding
(e.g.
ChIP-seq)
makes
supervised
inference
possible.
We
regard
as
a
graph-based
link
prediction
problem
that
expects
learn
low-dimensional
vectorized
representations
predict
potential
interactions.In
this
paper,
we
present
GENELink
latent
interactions
between
transcription
factors
(TFs)
target
genes
in
using
graph
attention
network.
projects
single-cell
expression
with
observed
TF-gene
pairs
space.
Then,
specific
learned
serve
downstream
similarity
measurement
causal
pairwise
by
optimizing
embedding
Compared
eight
existing
reconstruction
methods,
achieves
comparable
better
performance
on
seven
datasets
four
types
ground-truth
networks.
further
apply
human
breast
cancer
metastasis
reveal
heterogeneity
Notch
Wnt
signalling
pathways
primary
tumour
lung
metastasis.
Moreover,
ontology
enrichment
results
unique
indicate
mitochondrial
oxidative
phosphorylation
(OXPHOS)
is
functionally
important
during
seeding
step
metastatic
cascade,
which
validated
pharmacological
assays.The
code
available
https://github.com/zpliulab/GENELink.Supplementary
Bioinformatics
online.