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Novel Steroidal 5α,8α-Endoperoxide Derivatives with Semicarbazone/Thiosemicarbazone Side-chain as Apoptotic Inducers through an Intrinsic Apoptosis Pathway: Design, Synthesis and Biological Studies.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2020 Mar 07; Vol. 25 (5). Date of Electronic Publication: 2020 Mar 07. - Publication Year :
- 2020
-
Abstract
- A series of novel steroidal 5α,8α-endoperoxide derivatives bearing semicarbazone ( 7a - g ) or thiosemicarbazone ( 7h - k ) side chain were designed, synthesized and evaluated for their cytotoxicities in four human cancer cell lines (HepG2, HCT-116, MCF-7, and A549) using the MTT assay in vitro . The results showed that compound 7j exhibited significant cytotoxic activity against HepG2 cells (IC <subscript>50</subscript> = 3.52 μM), being more potent than ergosterol peroxide. Further cellular mechanism studies in HepG2 cells indicated that compound 7j triggered the mitochondrial-mediated apoptosis by decreasing mitochondrial membrane potential (MMP), which was associated with up-regulation of Bax, down-regulation of Bcl-2, activation levels of the caspase cascade, and formation of reactive oxygen species (ROS). The above findings indicated that compound 7j may be used as a promising skeleton for antitumor agents with improved efficacy.
- Subjects :
- Antineoplastic Agents chemistry
Apoptosis physiology
Caspases metabolism
Cell Line, Tumor
Drug Design
Drug Screening Assays, Antitumor
Hep G2 Cells
Humans
Membrane Potential, Mitochondrial drug effects
Oxidative Stress drug effects
Peroxides chemistry
Proto-Oncogene Proteins c-bcl-2 metabolism
Semicarbazones chemical synthesis
Semicarbazones pharmacology
Thiosemicarbazones chemical synthesis
Thiosemicarbazones chemistry
Thiosemicarbazones pharmacology
bcl-2-Associated X Protein metabolism
Antineoplastic Agents chemical synthesis
Antineoplastic Agents pharmacology
Apoptosis drug effects
Semicarbazones chemistry
Steroids chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 25
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 32156024
- Full Text :
- https://doi.org/10.3390/molecules25051209