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| LEADER |
13025nma a2204513 u 4500 |
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EB002048446 |
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EBX01000000000000001192112 |
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20240820000000.0 |
| 007 |
cr||||||||||||||||||||| |
| 008 |
220822 ||| eng |
| 020 |
|
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|a 9783036506319
|
| 020 |
|
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|a books978-3-0365-0631-9
|
| 020 |
|
|
|a 9783036506302
|
| 100 |
1 |
|
|a Honecker, Friedemann
|
| 245 |
0 |
0 |
|a Marine Compounds and Cancer 2020
|h Elektronische Ressource
|
| 260 |
|
|
|a Basel, Switzerland
|b MDPI - Multidisciplinary Digital Publishing Institute
|c 2021
|
| 300 |
|
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|a 1 electronic resource (480 p.)
|
| 653 |
|
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|a antioxidant
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| 653 |
|
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|a Lampetra morii
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| 653 |
|
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|a multidrug resistance
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| 653 |
|
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|a bromophenol
|
| 653 |
|
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|a apoptosis-inducing activity
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| 653 |
|
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|a cell adhesion molecules
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| 653 |
|
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|a ABC transporter
|
| 653 |
|
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|a p38α
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| 653 |
|
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|a Brevianamide
|
| 653 |
|
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|a Nur77
|
| 653 |
|
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|a humulane sesquiterpenoids
|
| 653 |
|
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|a AD0157
|
| 653 |
|
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|a p38/ERK
|
| 653 |
|
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|a NF-κB signaling
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| 653 |
|
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|a plakortide
|
| 653 |
|
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|a marine-derived drugs
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| 653 |
|
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|a fucoidan
|
| 653 |
|
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|a tumor microenvironment
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| 653 |
|
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|a trabectedin
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| 653 |
|
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|a non-small cell lung carcinoma
|
| 653 |
|
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|a FAU
|
| 653 |
|
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|a antiproliferative activity
|
| 653 |
|
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|a membrane permeabilization
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| 653 |
|
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|a fucoxanthin
|
| 653 |
|
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|a angiogenesis inhibitor
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| 653 |
|
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|a tumor cell line
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| 653 |
|
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|a mitochondria
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| 653 |
|
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|a kalkitoxin
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| 653 |
|
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|a sponges
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| 653 |
|
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|a PEL
|
| 653 |
|
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|a antitumour
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| 653 |
|
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|a human sarcoma cell line (HT1080 cells)
|
| 653 |
|
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|a PI3K/Akt
|
| 653 |
|
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|a cytoskeleton
|
| 653 |
|
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|a Penicillium brevicompactum
|
| 653 |
|
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|a endoperoxide
|
| 653 |
|
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|a non-small cell lung cancer
|
| 653 |
|
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|a marine antitumor agents
|
| 653 |
|
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|a cembranoids
|
| 653 |
|
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|a polyoxygenated steroids
|
| 653 |
|
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|a sipholenol A
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| 653 |
|
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|a jaspine B
|
| 653 |
|
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|a anthranilic acid
|
| 653 |
|
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|a prostate cancer
|
| 653 |
|
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|a SZ-685C
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| 653 |
|
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|a FBDD
|
| 653 |
|
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|a A375 and HeLa cell lines
|
| 653 |
|
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|a synergism
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| 653 |
|
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|a BEL-7402 cell
|
| 653 |
|
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|a gliotoxin
|
| 653 |
|
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|a natural marine compounds
|
| 653 |
|
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|a hydroxylated lipids
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| 653 |
|
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|a brominated indoles
|
| 653 |
|
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|a NF-κB
|
| 653 |
|
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|a seaweed
|
| 653 |
|
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|a phycocyanin
|
| 653 |
|
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|a arrest of cell cycle
|
| 653 |
|
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|a cancer
|
| 653 |
|
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|a anticarcinogenic
|
| 653 |
|
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|a epigonal organ
|
| 653 |
|
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|a caspase cascade
|
| 653 |
|
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|a lung cancer
|
| 653 |
|
|
|a antiangiogenic
|
| 653 |
|
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|a programmed cell death-ligand 2
|
| 653 |
|
|
|a cancer genes
|
| 653 |
|
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|a Lyngbya majuscula
|
| 653 |
|
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|a MRP1/ABCC1
|
| 653 |
|
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|a xyloketal B
|
| 653 |
|
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|a antiangiogenesis
|
| 653 |
|
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|a Penicillium paneum
|
| 653 |
|
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|a cyclin D1
|
| 653 |
|
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|a ET-743
|
| 653 |
|
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|a chromatography
|
| 653 |
|
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|a chemotherapy
|
| 653 |
|
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|a anti-metastatic activity
|
| 653 |
|
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|a sediment
|
| 653 |
|
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|a invasion
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| 653 |
|
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|a novel inhibitor
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| 653 |
|
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|a cytotoxicity
|
| 653 |
|
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|a proteomic
|
| 653 |
|
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|a proliferation
|
| 653 |
|
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|a pyrrolidinedione
|
| 653 |
|
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|a TGF-β signaling
|
| 653 |
|
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|a NSCLC
|
| 653 |
|
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|a circulating tumor cells
|
| 653 |
|
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|a Moorea producens
|
| 653 |
|
|
|a bioactive natural product
|
| 653 |
|
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|a antiproliferative
|
| 653 |
|
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|a HIF-1
|
| 653 |
|
|
|a cytotoxic activity
|
| 653 |
|
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|a microalgae
|
| 653 |
|
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|a mitochondria toxin
|
| 653 |
|
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|a ansamycins
|
| 653 |
|
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|a marine natural products
|
| 653 |
|
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|a cystatin F
|
| 653 |
|
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|a Porifera
|
| 653 |
|
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|a c-JUN
|
| 653 |
|
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|a n/a
|
| 653 |
|
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|a gemcitabine
|
| 653 |
|
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|a λ-carrageenan
|
| 653 |
|
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|a natural products
|
| 653 |
|
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|a anti-cancer
|
| 653 |
|
|
|a 3-alkylpyridinium polymers
|
| 653 |
|
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|a 12-deacetyl-12-epi-scalaradial
|
| 653 |
|
|
|a fascaplysin
|
| 653 |
|
|
|a cell adhesion
|
| 653 |
|
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|a inhibitor
|
| 653 |
|
|
|a autophagy inhibitors
|
| 653 |
|
|
|a neuroblastoma-rat sarcoma
|
| 653 |
|
|
|a ROS
|
| 653 |
|
|
|a energy stress
|
| 653 |
|
|
|a antifouling
|
| 653 |
|
|
|a glioblastoma
|
| 653 |
|
|
|a molecular docking
|
| 653 |
|
|
|a Streptomyces sp. SCSIO 11594
|
| 653 |
|
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|a cell cycle arrest
|
| 653 |
|
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|a poly(ADP-ribose)-polymerase inhibitor
|
| 653 |
|
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|a benzo[a]pyrene
|
| 653 |
|
|
|a pachastrissamine
|
| 653 |
|
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|a carotenoid
|
| 653 |
|
|
|a STAT3
|
| 653 |
|
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|a AP-1
|
| 653 |
|
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|a topoisomerase
|
| 653 |
|
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|a chemoprevention
|
| 653 |
|
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|a pheochromocytoma and paraganglioma
|
| 653 |
|
|
|a mechanisms of action
|
| 653 |
|
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|a polysaccharides
|
| 653 |
|
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|a selenium-containing polysaccharide-protein complex
|
| 653 |
|
|
|a CYP1A1
|
| 653 |
|
|
|a DNA minor groove binder
|
| 653 |
|
|
|a αO-conotoxin GeXIVA
|
| 653 |
|
|
|a SNORA62
|
| 653 |
|
|
|a chemosensitization
|
| 653 |
|
|
|a c-Met
|
| 653 |
|
|
|a marine sponges
|
| 653 |
|
|
|a anticancer immunity
|
| 653 |
|
|
|a β1-integrin
|
| 653 |
|
|
|a EMT
|
| 653 |
|
|
|a Topo I inhibitor
|
| 653 |
|
|
|a drug discovery
|
| 653 |
|
|
|a leukemia
|
| 653 |
|
|
|a marine drug
|
| 653 |
|
|
|a antibacterial
|
| 653 |
|
|
|a phlorotannins
|
| 653 |
|
|
|a p38
|
| 653 |
|
|
|a antitumor activities
|
| 653 |
|
|
|a puupehenones
|
| 653 |
|
|
|a cancer progression
|
| 653 |
|
|
|a fumigaclavine C
|
| 653 |
|
|
|a fatty acid 2-hydroxylase
|
| 653 |
|
|
|a manzamine A
|
| 653 |
|
|
|a CHOP
|
| 653 |
|
|
|a gene expression
|
| 653 |
|
|
|a marine organisms
|
| 653 |
|
|
|a breast cancer cells
|
| 653 |
|
|
|a sea anemone
|
| 653 |
|
|
|a anti-proliferation
|
| 653 |
|
|
|a heparanase
|
| 653 |
|
|
|a marine mollusc
|
| 653 |
|
|
|a Leathesia nana
|
| 653 |
|
|
|a soft tissue sarcoma
|
| 653 |
|
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|a divergolides
|
| 653 |
|
|
|a p65
|
| 653 |
|
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|a Cantabrian Sea-derived actinobacteria
|
| 653 |
|
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|a itampolin A
|
| 653 |
|
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|a soft coral
|
| 653 |
|
|
|a Ecklonia cava
|
| 653 |
|
|
|a programmed cell death
|
| 653 |
|
|
|a hypoxia
|
| 653 |
|
|
|a Marthasterias glacialis L.
|
| 653 |
|
|
|a hepatocellular carcinoma
|
| 653 |
|
|
|a cancer preventive
|
| 653 |
|
|
|a autophagy inducers
|
| 653 |
|
|
|a mitochondrial pathway
|
| 653 |
|
|
|a epithelial-mesenchymal transition
|
| 653 |
|
|
|a kunitz type inhibitor
|
| 653 |
|
|
|a glycosaminoglycans
|
| 653 |
|
|
|a safety
|
| 653 |
|
|
|a non-small cell lung cancer (NSCLC)
|
| 653 |
|
|
|a marine metabolites
|
| 653 |
|
|
|a TNFα
|
| 653 |
|
|
|a dibromotyrosine
|
| 653 |
|
|
|a carotenoids
|
| 653 |
|
|
|a cyclin-dependent kinase
|
| 653 |
|
|
|a cisplatin
|
| 653 |
|
|
|a nicotinic acetylcholine receptor
|
| 653 |
|
|
|a Sepia ink polysaccharides
|
| 653 |
|
|
|a pollution
|
| 653 |
|
|
|a MAPK/ERK pathway
|
| 653 |
|
|
|a HER2
|
| 653 |
|
|
|a small cell lung cancer
|
| 653 |
|
|
|a MCP-1
|
| 653 |
|
|
|a Haliclona gracilis
|
| 653 |
|
|
|a anti-angiogenic
|
| 653 |
|
|
|a thalassiolin B
|
| 653 |
|
|
|a clinical trials
|
| 653 |
|
|
|a bis (2,3-dibromo-4,5-dihydroxy-phenyl)-methane (BDDPM)
|
| 653 |
|
|
|a Isofistularin
|
| 653 |
|
|
|a gorgonian
|
| 653 |
|
|
|a antitumor
|
| 653 |
|
|
|a molecular oncology
|
| 653 |
|
|
|a human lung cancer
|
| 653 |
|
|
|a elisidepsin
|
| 653 |
|
|
|a P2X7 receptor
|
| 653 |
|
|
|a Akt
|
| 653 |
|
|
|a RGD motif
|
| 653 |
|
|
|a lung metastasis
|
| 653 |
|
|
|a uveal melanoma
|
| 653 |
|
|
|a secondary metabolites
|
| 653 |
|
|
|a bioanalysis
|
| 653 |
|
|
|a azoxymethane
|
| 653 |
|
|
|a reactive oxygen species
|
| 653 |
|
|
|a colorectal cancer
|
| 653 |
|
|
|a nanoparticle
|
| 653 |
|
|
|a chemical conjugation
|
| 653 |
|
|
|a naphthopyrones
|
| 653 |
|
|
|a human normal diploid fibroblast (TIG-1 cells)
|
| 653 |
|
|
|a sphingosine kinase inhibitor
|
| 653 |
|
|
|a TRPM7
|
| 653 |
|
|
|a depolymerisation
|
| 653 |
|
|
|a multi-drug resistant leukemia
|
| 653 |
|
|
|a heparan sulphate
|
| 653 |
|
|
|a therapeutic compounds
|
| 653 |
|
|
|a carcinoembryonic antigen
|
| 653 |
|
|
|a anti-proliferative
|
| 653 |
|
|
|a Antibody Drug Conjugates (ADCs)
|
| 653 |
|
|
|a araguspongine C
|
| 653 |
|
|
|a triterpene glycosides
|
| 653 |
|
|
|a melanoma
|
| 653 |
|
|
|a integrin β1
|
| 653 |
|
|
|a LS-1
|
| 653 |
|
|
|a low molecular weight fucoidan extract
|
| 653 |
|
|
|a molecular mechanisms
|
| 653 |
|
|
|a autophagy
|
| 653 |
|
|
|a migration
|
| 653 |
|
|
|a anticancer agent
|
| 653 |
|
|
|a Mycalin A
|
| 653 |
|
|
|a Micromonospora
|
| 653 |
|
|
|a evolution
|
| 653 |
|
|
|a molecular modeling
|
| 653 |
|
|
|a Tilapia piscidin 4 (TP4)
|
| 653 |
|
|
|a HeLa cells
|
| 653 |
|
|
|a sea cucumbers
|
| 653 |
|
|
|a natural product
|
| 653 |
|
|
|a targeted therapy
|
| 653 |
|
|
|a Medicine and Nursing / bicssc
|
| 653 |
|
|
|a Aspergillus
|
| 653 |
|
|
|a BCRP/ABCG2
|
| 653 |
|
|
|a cytokine release
|
| 653 |
|
|
|a C15 acetogenins
|
| 653 |
|
|
|a polyphenols
|
| 653 |
|
|
|a FAK
|
| 653 |
|
|
|a mitochondrial dysfunction
|
| 653 |
|
|
|a sinulariolide
|
| 653 |
|
|
|a anti-angiogenesis
|
| 653 |
|
|
|a pazopanib
|
| 653 |
|
|
|a terpenes
|
| 653 |
|
|
|a marangucyclines
|
| 653 |
|
|
|a Thalassia testudinum
|
| 653 |
|
|
|a α9-nicotinic acetylcholine receptors (nAChRs)
|
| 653 |
|
|
|a angiogenesis
|
| 653 |
|
|
|a cell cycle
|
| 653 |
|
|
|a dieckol
|
| 653 |
|
|
|a inflammation
|
| 653 |
|
|
|a Sarcophyton ehrenbergi
|
| 653 |
|
|
|a VEGF
|
| 653 |
|
|
|a tetracenomycin X
|
| 653 |
|
|
|a actinomycin
|
| 653 |
|
|
|a Cancer
|
| 653 |
|
|
|a chimera
|
| 653 |
|
|
|a glucocorticoid receptor
|
| 653 |
|
|
|a synthetic analogues
|
| 653 |
|
|
|a fatty acids
|
| 653 |
|
|
|a carbocyclic analogue
|
| 653 |
|
|
|a HSP90
|
| 653 |
|
|
|a Mycochromenic acid derivative
|
| 653 |
|
|
|a deep-sea
|
| 653 |
|
|
|a cell migration
|
| 653 |
|
|
|a N-Ras
|
| 653 |
|
|
|a nicotine
|
| 653 |
|
|
|a preclinical
|
| 653 |
|
|
|a hypoxia-inducible factor-1
|
| 653 |
|
|
|a anticoagulation
|
| 653 |
|
|
|a Jurkat
|
| 653 |
|
|
|a shrimp
|
| 653 |
|
|
|a pseudopterosin
|
| 653 |
|
|
|a A549 cells
|
| 653 |
|
|
|a Caribbean sponge
|
| 653 |
|
|
|a anticancer
|
| 653 |
|
|
|a JNK1/2
|
| 653 |
|
|
|a antitumoral
|
| 653 |
|
|
|a mangrove-derived actinomycete
|
| 653 |
|
|
|a marine fungus
|
| 653 |
|
|
|a anticoagulant
|
| 653 |
|
|
|a ribosomal protein genes
|
| 653 |
|
|
|a macrolide
|
| 653 |
|
|
|a marine biotechnology
|
| 653 |
|
|
|a anticancer activity
|
| 653 |
|
|
|a apoptosis
|
| 653 |
|
|
|a approved antitumor agents
|
| 653 |
|
|
|a hippuristanol
|
| 653 |
|
|
|a nonfunctioning pituitary adenomas
|
| 653 |
|
|
|a breast cancer
|
| 653 |
|
|
|a proteasomal degradation
|
| 653 |
|
|
|a camptothecin
|
| 653 |
|
|
|a sponge
|
| 653 |
|
|
|a endophytic fungus
|
| 653 |
|
|
|a virtual screening
|
| 653 |
|
|
|a palmitic acid
|
| 653 |
|
|
|a Aeroplysinin
|
| 653 |
|
|
|a cystatin superfamily
|
| 653 |
|
|
|a RPS30
|
| 653 |
|
|
|a porifera/sponge
|
| 653 |
|
|
|a snoRNA
|
| 653 |
|
|
|a paulomycins
|
| 653 |
|
|
|a cooperative binding
|
| 653 |
|
|
|a metastasis
|
| 653 |
|
|
|a Ulva fasciata
|
| 653 |
|
|
|a programmed cell death-ligand 1
|
| 653 |
|
|
|a tumor-associated macrophages
|
| 653 |
|
|
|a lipid rafts
|
| 653 |
|
|
|a marine drugs
|
| 653 |
|
|
|a oxidative stress
|
| 653 |
|
|
|a IL-6
|
| 653 |
|
|
|a Antimicrobial peptide (AMP)
|
| 653 |
|
|
|a low toxic
|
| 653 |
|
|
|a isatin
|
| 653 |
|
|
|a Leptogorgia
|
| 653 |
|
|
|a bonnethead shark
|
| 653 |
|
|
|a osteosarcoma
|
| 653 |
|
|
|a endothelial cells
|
| 653 |
|
|
|a hybridization
|
| 653 |
|
|
|a P-gp/ABCB1
|
| 653 |
|
|
|a ER-stress
|
| 653 |
|
|
|a in vivo model
|
| 653 |
|
|
|a SNU-C5/5-FU
|
| 653 |
|
|
|a phase I
|
| 653 |
|
|
|a signal transduction
|
| 653 |
|
|
|a plitidepsin
|
| 653 |
|
|
|a adriamycin resistance
|
| 653 |
|
|
|a marine compound
|
| 653 |
|
|
|a chemopreventive
|
| 653 |
|
|
|a buccal gland
|
| 700 |
1 |
|
|a Dyshlovoy, Sergey A.
|
| 700 |
1 |
|
|a Honecker, Friedemann
|
| 700 |
1 |
|
|a Dyshlovoy, Sergey A.
|
| 041 |
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|a eng
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|b DOAB
|a Directory of Open Access Books
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|a Creative Commons (cc), https://creativecommons.org/licenses/by/4.0/
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|a 10.3390/books978-3-0365-0631-9
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|u https://www.mdpi.com/books/pdfview/book/3853
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|x Verlag
|3 Volltext
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|u https://directory.doabooks.org/handle/20.500.12854/76418
|z DOAB: description of the publication
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|a The very first marine-derived anticancer drug, Cytarabine (aka Ara-C, Cytosar-U®), was approved by the FDA in 1969 for the treatment of leukemia. At the beginning of 2021, the list of approved marine-derived anticancer drugs consists of nine substances, five of which received approval within the last two years, demonstrating the rapid evolution of the field. The current book is a collection of scientific articles related to the exponentially growing field of anticancer marine compounds. These articles cover the whole field, from agents with cancer-preventive activity, to novel and previously characterized compounds with anticancer activity, both in vitro and in vivo, as well as the latest status of compounds under clinical development.
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