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17β-Hydroxywithanolides as Sensitizers of Renal Carcinoma Cells to Tumor Necrosis Factor-α Related Apoptosis Inducing Ligand (TRAIL) Mediated Apoptosis: Structure-Activity Relationships.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2017 Apr 13; Vol. 60 (7), pp. 3039-3051. Date of Electronic Publication: 2017 Mar 21. - Publication Year :
- 2017
-
Abstract
- Renal cell carcinoma (RCC) is a cancer with poor prognosis, and the 5-year survival rate of patients with metastatic RCC is 5-10%. Consequently, treatment of metastatic RCC represents an unmet clinical need. Screening of a 50 000-member library of natural and synthetic compounds for sensitizers of RCC cells to TRAIL-mediated apoptosis led to identification of the 17β-hydroxywithanolide (17-BHW), withanolide E (1), as a promising lead. To explore structure-activity relationships, we obtained natural and semisynthetic withanolides 1, 2a, 2c, and 3-36 and compared their ability to sensitize TRAIL-mediated apoptosis in a panel of renal carcinoma cells. Our findings revealed that 17-BHWs with a α-oriented side chain are superior to known TRAIL-sensitizing withanolides belonging to withaferin A class with a β-oriented side chain and demonstrated that the 17-BHW scaffold can be modified to enhance sensitization of RCCs to TRAIL-mediated apoptosis, thereby assisting development of natural-product-inspired drugs to treat metastatic RCC.
- Subjects :
- Antineoplastic Agents, Phytogenic chemistry
Carcinoma, Renal Cell metabolism
Carcinoma, Renal Cell pathology
Cell Line, Tumor
Ergosterol chemistry
Ergosterol pharmacology
Humans
Kidney metabolism
Kidney pathology
Kidney Neoplasms metabolism
Kidney Neoplasms pathology
Structure-Activity Relationship
Withania chemistry
Withanolides chemistry
Antineoplastic Agents, Phytogenic pharmacology
Apoptosis drug effects
Carcinoma, Renal Cell drug therapy
Ergosterol analogs & derivatives
Kidney Neoplasms drug therapy
TNF-Related Apoptosis-Inducing Ligand metabolism
Withanolides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 60
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 28257574
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.7b00069