<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>53</viewCount><searchCount>0</searchCount></scores><additional><submitter>Xu YM</submitter><funding>Arizona Biomedical Research Commission</funding><funding>Intramural NIH HHS</funding><funding>College of Agriculture and Life Sciences, University of Arizona</funding><funding>National Cancer Institute</funding><pagination>3039-3051</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6986374</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>60(7)</volume><pubmed_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.</pubmed_abstract><journal>Journal of medicinal chemistry</journal><pubmed_title>17β-Hydroxywithanolides as Sensitizers of Renal Carcinoma Cells to Tumor Necrosis Factor-α Related Apoptosis Inducing Ligand (TRAIL) Mediated Apoptosis: Structure-Activity Relationships.</pubmed_title><pmcid>PMC6986374</pmcid><funding_grant_id>HHSN26120080001E</funding_grant_id><funding_grant_id>Z01 BC010012</funding_grant_id><pubmed_authors>Sayers TJ</pubmed_authors><pubmed_authors>Henrich CJ</pubmed_authors><pubmed_authors>Tewary P</pubmed_authors><pubmed_authors>Xu YM</pubmed_authors><pubmed_authors>Gunatilaka AA</pubmed_authors><pubmed_authors>Brooks AD</pubmed_authors><pubmed_authors>Wijeratne EM</pubmed_authors><view_count>53</view_count></additional><is_claimable>false</is_claimable><name>17β-Hydroxywithanolides as Sensitizers of Renal Carcinoma Cells to Tumor Necrosis Factor-α Related Apoptosis Inducing Ligand (TRAIL) Mediated Apoptosis: Structure-Activity Relationships.</name><description>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.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Apr</publication><modification>2024-11-10T03:29:09.124Z</modification><creation>2020-10-29T16:06:22Z</creation></dates><accession>S-EPMC6986374</accession><cross_references><pubmed>28257574</pubmed><doi>10.1021/acs.jmedchem.7b00069</doi></cross_references></HashMap>