| Literature DB >> 33477536 |
Nader N El-Chaar1, Thomas E Smith2, Gajendra Shrestha1, Stephen R Piccolo3, Mary Kay Harper2, Ryan M Van Wagoner2, Zhenyu Lu2, Ashlee R Venancio2, Chris M Ireland2, Andrea H Bild1,4, Philip J Moos1.
Abstract
Patients diagnosed with basal-like breast cancer suffer from poor prognosis and limited treatment options. There is an urgent need to identify new targets that can benefit patients with basal-like and claudin-low (BL-CL) breast cancers. We screened fractions from our Marine Invertebrate Compound Library (MICL) to identify compounds that specifically target BL-CL breast cancers. We identified a previously unreported trisulfated sterol, i.e., topsentinol L trisulfate (TLT), which exhibited increased efficacy against BL-CL breast cancers relative to luminal/HER2+ breast cancer. Biochemical investigation of the effects of TLT on BL-CL cell lines revealed its ability to inhibit activation of AMP-activated protein kinase (AMPK) and checkpoint kinase 1 (CHK1) and to promote activation of p38. The importance of targeting AMPK and CHK1 in BL-CL cell lines was validated by treating a panel of breast cancer cell lines with known small molecule inhibitors of AMPK (dorsomorphin) and CHK1 (Ly2603618) and recording the increased effectiveness against BL-CL breast cancers as compared with luminal/HER2+ breast cancer. Finally, we generated a drug response gene-expression signature and projected it against a human tumor panel of 12 different cancer types to identify other cancer types sensitive to the compound. The TLT sensitivity gene-expression signature identified breast and bladder cancer as the most sensitive to TLT, while glioblastoma multiforme was the least sensitive.Entities:
Keywords: AMPK; CHK1; breast cancer; drug susceptibility; topsentinol L trisulfate
Year: 2021 PMID: 33477536 PMCID: PMC7831112 DOI: 10.3390/md19010041
Source DB: PubMed Journal: Mar Drugs ISSN: 1660-3397 Impact factor: 5.118