Substituted 2-hydroxy-N-(arylalkyl)benzamide sensitizes cancer cells to metabolic stress by disrupting actin cytoskeleton and inhibiting autophagic flux
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
27612957
DOI
10.1016/j.tiv.2016.09.006
PII: S0887-2333(16)30179-5
Knihovny.cz E-resources
- Keywords
- Actin, Autophagy, Melanoma, Metabolic stress, Sorafenib, Substituted 2-hydroxy-N-(arylalkyl)benzamide,
- MeSH
- Apoptosis drug effects MeSH
- Autophagy drug effects MeSH
- Benzamides pharmacology MeSH
- Cell Line MeSH
- Cell Cycle drug effects MeSH
- Phenylalanine analogs & derivatives pharmacology MeSH
- Phenylurea Compounds pharmacology MeSH
- Stress, Physiological MeSH
- Wound Healing MeSH
- Protein Kinase Inhibitors pharmacology MeSH
- Humans MeSH
- Actin Cytoskeleton drug effects MeSH
- Cell Line, Tumor MeSH
- Niacinamide analogs & derivatives pharmacology MeSH
- Cell Proliferation drug effects MeSH
- Antineoplastic Agents pharmacology MeSH
- Sorafenib MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Benzamides MeSH
- Phenylalanine MeSH
- Phenylurea Compounds MeSH
- Protein Kinase Inhibitors MeSH
- N-(1-(4-chlorophenylcarbamoyl)-2-phenylethyl)-5-chloro-2-hydroxybenzamide MeSH Browser
- Niacinamide MeSH
- Antineoplastic Agents MeSH
- Sorafenib MeSH
N-((R)-1-(4-chlorophenylcarbamoyl)-2-phenylethyl)-5-chloro-2-hydroxybenzamide (Compound 6k), was recently isolated during the preparation of amino acids esters with salicylanilides. We show here that 6k disrupts the dynamics of actin cytoskeleton in human melanoma cells, affecting processes essential for the maintenance and expansion of tumours such as cell adhesion, motility, proliferation, vesicular transport, and autophagic flux. We demonstrated that inhibition of autophagy by 6k increased the sensitivity of melanoma cells to metabolic stress induced by rotenone or nutrient starvation and potentiated the anti-proliferative activity of small molecule multikinase inhibitor sorafenib. Since autophagy plays an important role in survival of cancer cells subjected to chemotherapy, the above mentioned properties are interesting from clinical point of view as 6k could promote metabolic stress within the tumour microenvironment and potentiate the effect of cytostatics in combination therapy.
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