A potentiated cooperation of carbonic anhydrase IX and histone deacetylase inhibitors against cancer.
Antigens, Neoplasm
/ metabolism
Antineoplastic Agents
/ chemical synthesis
Carbonic Anhydrase IX
/ antagonists & inhibitors
Carbonic Anhydrase Inhibitors
/ chemical synthesis
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Dose-Response Relationship, Drug
Drug Screening Assays, Antitumor
Histone Deacetylase Inhibitors
/ chemical synthesis
Histone Deacetylases
/ metabolism
Humans
Molecular Structure
Phenylurea Compounds
/ chemical synthesis
Structure-Activity Relationship
Sulfonamides
/ chemical synthesis
Tumor Cells, Cultured
Carbonic anhydrase IX
SLC-0111;SAHA
combined therapy
histone acetylation
Journal
Journal of enzyme inhibition and medicinal chemistry
ISSN: 1475-6374
Titre abrégé: J Enzyme Inhib Med Chem
Pays: England
ID NLM: 101150203
Informations de publication
Date de publication:
Dec 2020
Dec 2020
Historique:
entrez:
24
12
2019
pubmed:
24
12
2019
medline:
15
2
2020
Statut:
ppublish
Résumé
The emergence of tumour recurrence and resistance limits the survival rate for most tumour-bearing patients. Only, combination therapies targeting pathways involved in the induction and in the maintenance of cancer growth and progression might potentially result in an enhanced therapeutic efficacy. Herein, we provided a prospective combination treatment that includes suberoylanilide hydroxamic acid (SAHA), a well-known inhibitor of histone deacetylases (HDACs), and SLC-0111, a novel inhibitor of carbonic anhydrase (CA) IX. We proved that HDAC inhibition with SAHA in combination with SLC-0111 affects cell viability and colony forming capability to greater extent than either treatment alone of breast, colorectal and melanoma cancer cells. At the molecular level, this therapeutic regimen resulted in a synergistically increase of histone H4 and p53 acetylation in all tested cell lines. Overall, our findings showed that SAHA and SLC-0111 can be regarded as very attractive combination providing a potential therapeutic strategy against different cancer models.
Identifiants
pubmed: 31865754
doi: 10.1080/14756366.2019.1706090
pmc: PMC6968260
doi:
Substances chimiques
Antigens, Neoplasm
0
Antineoplastic Agents
0
Carbonic Anhydrase Inhibitors
0
Histone Deacetylase Inhibitors
0
Phenylurea Compounds
0
SLC-0111
0
Sulfonamides
0
Histone Deacetylases
EC 3.5.1.98
CA9 protein, human
EC 4.2.1.1
Carbonic Anhydrase IX
EC 4.2.1.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
391-397Références
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