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Structures/cytotoxicity/selectivity relationship of natural steroidal saponins against GSCs and primary mechanism of tribulosaponin A
- Source :
- European journal of medicinal chemistry. 210
- Publication Year :
- 2020
-
Abstract
- Glioblastoma multiform (GBM) is the highly aggressive brain tumor with poor prognosis. Glioma stem cells (GSCs), small population of cancer cells that exist in GBM tissues, resistant to chemotherapy and radiotherapy and usually driving GBM recurrence, have been developed as effective therapeutic target. Steroidal saponins are one of important resources for anti-tumor agent and may be benefited to selectively clear GSCs. In this report, total of 97 natural steroidal saponins were investigated the relationship among structures/cytotoxicity/selectivity against GSCs, glioma cell lines and human untransformed cells, and revealed that tribulosaponin A was the most potent compound. Further investigation suggested that tribulosaponin A up-regulated the expression of NCF1 and NOX1 to accumulate ROS for triggering apoptosis in GSCs, but not in untransformed cells, and it was further supported by the assay that N-acetyl-l-cysteine (NAC) clearing ROS delayed GSCs apoptosis. Besides, tribulosaponin A damaged GSCs recapturing tumor spheres formation.
- Subjects :
- endocrine system
Cell Survival
medicine.medical_treatment
Population
Brain tumor
Antineoplastic Agents
Apoptosis
01 natural sciences
03 medical and health sciences
Structure-Activity Relationship
Glioma
Drug Discovery
medicine
Tumor Cells, Cultured
Humans
Cytotoxicity
education
030304 developmental biology
Cell Proliferation
Pharmacology
0303 health sciences
Chemotherapy
education.field_of_study
Biological Products
Dose-Response Relationship, Drug
Molecular Structure
010405 organic chemistry
Chemistry
Brain Neoplasms
fungi
Organic Chemistry
General Medicine
Saponins
medicine.disease
0104 chemical sciences
Goosecoid Protein
Cancer cell
Cancer research
Stem cell
Drug Screening Assays, Antitumor
Glioblastoma
Subjects
Details
- ISSN :
- 17683254
- Volume :
- 210
- Database :
- OpenAIRE
- Journal :
- European journal of medicinal chemistry
- Accession number :
- edsair.doi.dedup.....41424a1f63aec7e4e371c0edca690194