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Advances and Novel Treatment Options in Metastatic Melanoma
Advances and Novel Treatment Options in Metastatic Melanoma
Autore Facchiano Antonio
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (528 p.)
Soggetto topico Medicine
Soggetto non controllato melanoma
invasion
WNT5A
MARCKS
phosphorylation
MANS peptide
nanoparticles
cell therapy
tumor microenvironment
sex/gender
sex-hormones
immunity
microRNAs
immunotherapy
BRAF-mutant melanoma
BRAF inhibitor
mechanism of action
targeted therapy
tumour microenvironment
plasmacytoid dendritic cells
lactate dehydrogenase
TLR
interferon
CXCL10
TPC2
HIPPO
SOCE
metastasis
essential oils
angiogenesis
apoptosis
uveal melanoma (UM)
metastatic uveal melanoma (mUM)
prognostication
adjuvant therapy
metastatic therapy
metastatic dormancy
liver-directed-therapies
targeted-therapy
combined therapy
protein tyrosine phosphatase
PTPs inhibitors
melanoma immune infiltrate
BRAF inhibitors
microenvironment
resistance
therapy
therapeutic resistance
exosomes
extracellular vesicles
diagnosis
prognosis
ctDNA
liquid biopsy
prediction
patient stratification
BRAF
arthralgia
rheumatoid arthritis
carbonic anhydrase
hedgehog
cyclopamine
small molecules
acetazolamide
motility
metalloproteinases
FAK
cancer
mucosal melanoma
nivolumab
pembrolizumab
ipilimumab
radiotherapy
cholinergic system
acetylcholine
muscarinic receptors
nicotinic receptors
melanoma metastasis
ShcD adaptor protein
amoeboid motility
Rac1
DOCK4
melanoma PDX
target therapy
cancer stem cells
slow cycling phenotype
drug resistance
OXPHOS
lipid metabolism
cancer associated fibroblast
melanomagenesis
biomarkers
checkpoint inhibitor
PD-1
melanoma markers
cytokines
machine learning
Support Vector Machine
principal component analysis
BCL2L10
STAT3
cytotoxicity
survival
ABT-737
Bcl-2 family
ML258
HuR
MITF
metastases
siRNA
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557612103321
Facchiano Antonio  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Molecular Pathways in Cancers
Molecular Pathways in Cancers
Autore Cristóbal Ion
Pubbl/distr/stampa Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica 1 electronic resource (284 p.)
Soggetto topico Medicine
Oncology
Soggetto non controllato actin cytoskeletal reorganization
breast cancer
CD99 agonist
EGFR dimerization
endocytosis
FAK dephosphorylation
PTPN12
Rac1
RhoA
tripeptide
OMD
PRELP
tumor suppression gene
bladder cancer initiation
tight junction
partial EMT
tousled-like kinase (TLK)
NIMA-related kinase 1 (NEK1)
yes-associated protein 1 (YAP1)
thioridazine (THD)
MS-determined phosphopeptides
human immunodeficiency virus type 1
epithelial cells
carcinogenicity
oxidative stress
reactive oxygen species
gp120
Tat
Nef
matrix protein p17
reverse transcriptase
mitochondria
metastasis
OXPHOS
cancer
Warburg effect
cancer therapeutics
myeloproliferative neoplasms
signaling pathways
JAK2
CALR
MPL
TPOR
DUSP1
MAPK
Snail
prostate cancer
migration and invasion
patient survival
biomarkers
pBRD4
SET
PP2A
prognosis
triple negative breast cancer
resistance
anti-receptor therapy
trastuzumab
PI3K
mTOR
TAK-228
epigenetic
methylation
acetylation
non-coding RNA
small-cell lung cancer
triple-negative breast cancer
pancreatic ductal adenocarcinoma
glioblastoma
metastatic melanoma
advanced ovarian cancer
hepatocellular carcinoma
immune evasion
immunotherapy
immune checkpoint inhibitors
oncogenic signaling pathway
molecular targeted agents
genome
epigenome
tumor immune microenvironment
ovarian cancer
adaptive immunity
innate immunity
complement system
cancer immunology
tumor microenvironment
splicing pathway
luminal breast cancer
BET inhibitors
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910566473703321
Cristóbal Ion  
Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui