The Immune Environment in Colorectal Adenoma: A Systematic Review
Biomedicines,
Journal Year:
2025,
Volume and Issue:
13(3), P. 699 - 699
Published: March 12, 2025
Background/Objectives:
Research
on
colorectal
adenoma
is
significantly
less
comprehensive
compared
to
studies
carcinoma.
Although
a
precursor
of
the
majority
sporadic
cancers,
not
all
adenomas
develop
into
carcinomas.
The
complex
interaction
immune
responses
in
premalignant
tumor
microenvironment
might
be
factor
for
that.
Methods:
In
this
systematic
review,
we
aim
provide
thorough
analysis
current
research
examining
infiltration
patterns
tissues
context
cell-based,
cytokine-based,
and
other
immunological
factor-related
changes
along
conventional
adenoma–carcinoma
sequence.
articles
included
review
extend
up
December
2024
PubMed
Web
Science
databases.
Results:
Most
have
shown
significant
differences
cell
counts,
densities,
cytokine
expression
levels
associated
with
lesions
(and/or
cancer).
No
consensus
immune-related
tendencies
concerning
CD4+T
cells
CD8+T
was
reached.
Decreasing
mDCs
plasma
naïve
B
were
detected
ACS.
increased
density
tissue
eosinophils
dramatically
diminishes
after
transition
As
progresses,
increasing
IL-1α,
IL-4,
IL-6,
IL-8,
IL-10,
IL-17A,
IL-21,
IL-23,
IL-33,
TGF-β
decreasing
IL-12A,
IL-18,
IFN—γ,
TNFα
cytokines
invasive
carcinoma
stage
being
detected.
over-expression
COX-2,
PD-1/PD-L1,
CTLA-4,
ICOS/ICOSLG
adenomatous
cancerous
also
observed.
Conclusions:
Further
are
needed
better
understanding
whole
picture
adenoma-associated
immunity
its
impact
precancerous
lesion’s
potential
progress.
Language: Английский
Unraveling BRAF alterations: molecular insights to circumvent therapeutic resistance across cancer types
Caterina Perfetto,
No information about this author
Marianna Aprile,
No information about this author
Simona Cataldi
No information about this author
et al.
Cancer Drug Resistance,
Journal Year:
2025,
Volume and Issue:
unknown
Published: March 24, 2025
Aim:
As
intrinsic
resistance
-
often
driven
by
concurrent
genomic
alterations
in
tumor
suppressor
genes
or
oncogenes
remains
a
major
challenge
oncology,
this
work
aimed
to
comprehensively
analyze
BRAF
somatic
across
cancer
types
and
identify
new
potential
therapeutic
strategies
overcome
drug
resistance.
Methods:
We
conducted
an
extensive
analysis
of
genomics,
transcriptomics,
clinical
data
retrieved
from
public
repositories,
including
cBioPortal.
Our
comprehensive
examined
[point
mutations,
structural
variants
(SVs)
copy
number
alteration]
more
than
217,000
samples
120
distinct
primary
metastatic
sites
both
adult
pediatric
cohorts,
focusing
on
mutual
exclusivity
co-occurrence
mutations
other
suppressors.
The
also
explores
the
association
with
survival,
molecular
features.
Results:
Analysis
mutation
frequencies
revealed
that
BRAFV600E
represents
approximately
90%
all
alterations.
While
melanoma
thyroid
carcinoma
show
highest
prevalence
followed
colorectal
non-small
cell
lung
terms
absolute
patients
harboring
worldwide,
notably
high
were
identified
rare
malignancies,
hairy-cell
leukemia,
ganglioglioma,
serous
borderline
ovarian
tumors.
profiling
these
tumors
uncovered
patterns
co-occurring
mutually
exclusive
genes,
illuminating
mechanisms
suggesting
novel
combinations.
Conclusion:
Comprehensive
is
critical
for
optimizing
targeted
therapy
overcoming
-mutated
cancers.
identification
provides
opportunities
rational
combination
therapies,
emphasizing
importance
detailed
developing
effective
treatment
diverse
types.
Language: Английский
Drugs Discovery from Traditional Phytotherapy
Biswajit Patra,
No information about this author
Anil Biswal
No information about this author
Published: April 29, 2025
BACKGROUND.
Phytotherapy
refers
to
the
use
of
plant
extracts
for
therapeutic
purpose.
It
plays
important
role
in
ancient
medicine
practices.
has
been
considered
as
a
cornerstone
development
modern
drugs.
With
advancement
field
science
and
technology,
researchers
systematically
evaluate
medicinal
properties
plants.
OBJECTIVE.
is
an
integrative
approach
that
integrates
traditional
knowledge
with
techniques
identification,
isolation,
test
derivative
compounds.
Literature
on
plant-derived
natural
products
used
suitable
precursors
drug
discovery
was
included.
METHODS.
The
data
source
were
obtained
through
literature
publications
using
different
scientific
search
engines.
RESULTS.
These
papers
carefully
evaluated,
critically
analyzed
structured
accurate
information.
process
begins
ethnobotanical
surveys
study
select
promising
potential
herb.
Phytochemical
methods
are
then
employed
extract
isolate
active
constituents.
phytotherapy
drugs
have
plants
support
health
manage
various
conditions.
Recently
analytical
chemistry
genomics
essential
accelerating
process.
High-throughput
screening,
molecular
docking,
bioinformatics
tools
enabled
rapid
identification
bioactive
Traditional
significantly
influenced
by
providing
wealth
about
plant-based
remedies.
Many
pharmaceuticals
roots
herbal
practices,
compounds
isolated
from
forming
basis
effective
treatments.
CONCLUSION.
This
integration
wisdom
research
led
targeted
therapies,
emphasizing
importance
discovery.
As
continue
explore
compounds,
remains
vital
new
medicines.
Moreover,
advancements
pharmacokinetics
pharmacodynamics
improved
understanding
interact
biological
systems,
enhancing
their
efficacy
safety
profiles.
Language: Английский
CRISPR/Cas9-directed epigenetic editing in colorectal cancer
Manoj Gupta,
No information about this author
Gayatri Gouda,
No information about this author
Maryam Moazzam‐Jazi
No information about this author
et al.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer,
Journal Year:
2025,
Volume and Issue:
unknown, P. 189338 - 189338
Published: April 1, 2025
Language: Английский
Exploring the molecular mechanisms and therapeutic potential of SMAD4 in colorectal cancer
Hui Shan,
No information about this author
Guangyu Tian,
No information about this author
Yeqing Zhang
No information about this author
et al.
Cancer Biology & Therapy,
Journal Year:
2024,
Volume and Issue:
25(1)
Published: Aug. 20, 2024
Colorectal
Cancer
(CRC)
is
the
third
most
common
cancer
worldwide,
and
occurrence
development
of
CRC
are
influenced
by
molecular
biology
characteristics
CRC,
especially
alterations
in
key
signaling
pathways.
The
transforming
growth
factor-β
(TGF-β)
plays
a
crucial
role
cellular
growth,
differentiation,
migration,
apoptosis,
with
SMAD4
protein
serving
as
transcription
factor
TGF-β
pathway,
thus
playing
significant
onset
progression
CRC.
one
malignancies
high
mortality
rate
worldwide.
Despite
research
progress
recent
years,
regarding
SMAD4,
its
dual
early
late
stages
tumor
has
promoted
further
discussion
on
complexity
therapeutic
target,
highlighting
urgent
need
for
deeper
analysis
This
review
aims
to
explore
function
potential
target.
Language: Английский
Association between the expression level of miRNA‑374a and TGF‑β1 in patients with colorectal cancer
World Academy of Sciences Journal,
Journal Year:
2024,
Volume and Issue:
6(6)
Published: Oct. 7, 2024
Colorectal
cancer
(CRC)
poses
a
significant
threat
to
global
health
with
increasing
incidence
and
mortality
rates.
Exploring
different
molecular
mechanisms
aspects
underlying
the
development
progression
of
CRC
will
promote
early
diagnosis
lead
better
outcomes.
MicroRNAs
(miRNAs/miRs)
are
one
related
CRC.
The
present
study
aimed
investigate
association
between
expression
levels
miRNA‑374a
transforming
growth
factor
(TGF)‑β1
in
patients
explore
roles
these
markers
carcinogenesis
their
use
as
diagnostic
biomarkers.
For
this
purpose,
195
subjects
were
enrolled.
level
was
assessed
serum
samples
145
(screening
phase)
addition
50
tissue
validate
tumor‑derived
(confirmation
phase).
analysis
performed
by
extraction
miRNAs
followed
reverse
transcription‑quantitative
PCR.
Additionally,
TGF‑β1
measured
all
control
samples.
ROC
curve
determine
potential
TGF‑β1.
exhibited
significantly
elevated
compared
healthy
individuals,
fold
change
12.92
(P=0.0001).
Moreover,
varied,
depending
on
grade;
grade
I
disease
9.2‑fold
increase
those
II
21.84‑fold
expression.
relative
tissues
upregulated
4.48‑fold
adjacent
non‑cancerous
(P<0.001).
Furthermore,
controls
area
under
0.9560
for
(P<0.0001),
0.8972
(P<0.0001)
0.8075
(P=0.001).
In
addition,
positive
correlation
found
miRNA‑374
(Rho=0.8912,
P=<0.0001).
On
whole,
demonstrates
that
indicate
crucial
driving
tumor
highlight
biomarkers
therapeutic
targets
Language: Английский