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Metastatic Progression and Tumour Heterogeneity
Metastatic Progression and Tumour Heterogeneity
Autore Hollande Fred
Pubbl/distr/stampa Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica 1 online resource (312 p.)
Soggetto topico Medicine and Nursing
Soggetto non controllato 3D cultures
acidosis
ADH
angiocrine factor
beta-catenin paradox
biomechanics
breast cancer
carbonic anhydrase
cell fate
cellular heterogeneity
circulating tumor cells
circulating tumor cells (CTCs)
clear cell renal cell carcinoma
clonality
collective and single-cell migration
colon cancer
colorectal cancer
CTC-clusters
DCIS
deficient mismatch repair
EMT
endometrial carcinoma
epigenetics
epithelial mesenchymal plasticity
epithelial-to-mesenchymal transition
esophageal squamous cell carcinoma
extracellular vesicles
gene expression
genomics
heterogeneity
hybrid E/M
hyperpolarized 13C MRI
immune checkpoints
immune microenvironment
immunotherapy
interstitial pH
intra-tumour heterogeneity
intratumor heterogeneity
lactic acid
magnetic resonance imaging
mammary gland
metaplastic carcinoma
metastasis
metastatic niche
microsatellite instability
miRNA expression
multisite tumor sampling
mutation
natural killer cells
nuclear medicine
organoids
pancreatic cancer
PET
phenotypic plasticity
PI3K/AKT pathway
plasticity
positron emission tomography
precision medicine
radiomics
radiopharmaceuticals
review
signaling
single-cell analysis
single-cell RNAseq
subclonal diversity
SUV
target discovery
targeted therapy
TP53
treatment resistance
tumor ecology
tumor endothelial cell
tumor evolution
tumor heterogeneity
tumor microenvironment
tumor mutation burden
uterine carcinosarcoma
Wnt signaling
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910557105803321
Hollande Fred  
Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Updates on Molecular Targeted Therapies for CNS Tumors
Updates on Molecular Targeted Therapies for CNS Tumors
Pubbl/distr/stampa MDPI - Multidisciplinary Digital Publishing Institute, 2023
Descrizione fisica 1 online resource (368 p.)
Soggetto topico Medicine and Nursing
Oncology
Soggetto non controllato A172
A2AAR antagonist
adenosine
adenosine receptors
antigen processing and presentation
antioxidant
apoptosis
ATRX
bevacizumab
biomarker
blood-brain barrier
brain metastasis
brain tumor
cancer metabolism
cell cycle arrest
central nervous system
chemotherapy
CNS disease
CNS lymphoma
CpG island
diffuse midline gliomas
DNMT
EGFR
ependymoma
EPHB2
epidermal growth factor receptor
ERK/MAPK pathway
FGFR3
G-CIMP
GBM
germline mutation
glioblastoma
glioblastoma molecular classification
glioma
Group A
Group B
H3K27M
histone acetylation
IDH-mutant glioma
immune evasion
immune score
immunotherapy
intraparenchymal metastases
intrathecal
isotope labeling
KIF11
leptomeningeal
low grade glioma
low-grade glioma
LPS
lung cancer
lung carcinoma
lung malignancy
mass spectrometry
meningitis
MET
metastatic disease
Metformin
methotrexate
methylation
methylomics
methyltransferases
MGMT
molecular targets
molecular therapy
monoclonal antibodies
MYCN
myxopapillary
n/a
neoantigen
neoplastic
neurofibromatosis
NF1
novel therapeutics
novel therapies
patient avatars
PCNSL
PDGFRA
pediatric brain tumor
PFA
PFB
PI3K/PTEN pathway
plexiform neurofibroma
potential therapy development
preclinical models
progression
progression-free survival
radiotherapy
receptor tyrosine kinase
RELA
stereotactic radiosurgery
subependymoma
T cells
T lymphocytes
targeted therapy
temozolomide
tumor microenvironment
tumor mutation burden
tumor suppressor
tyrosine kinase inhibitors
U87MG
vestibular schwannoma
Warburg effect
whole-brain radiation therapy
YAP1
ZFTA
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9911053032003321
MDPI - Multidisciplinary Digital Publishing Institute, 2023
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui