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Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers.
El-Chaar, Nader N; Smith, Thomas E; Shrestha, Gajendra; Piccolo, Stephen R; Harper, Mary Kay; Van Wagoner, Ryan M; Lu, Zhenyu; Venancio, Ashlee R; Ireland, Chris M; Bild, Andrea H; Moos, Philip J.
Afiliação
  • El-Chaar NN; Department of Pharmacology and Toxicology, University of Utah, Salt Lake, UT 84112, USA.
  • Smith TE; Department of Medicinal Chemistry, University of Utah, Salt Lake, UT 84112, USA.
  • Shrestha G; Department of Pharmacology and Toxicology, University of Utah, Salt Lake, UT 84112, USA.
  • Piccolo SR; The College of Life Sciences, Brigham Young University, Provo, UT 84606, USA.
  • Harper MK; Department of Medicinal Chemistry, University of Utah, Salt Lake, UT 84112, USA.
  • Van Wagoner RM; Department of Medicinal Chemistry, University of Utah, Salt Lake, UT 84112, USA.
  • Lu Z; Department of Medicinal Chemistry, University of Utah, Salt Lake, UT 84112, USA.
  • Venancio AR; Department of Medicinal Chemistry, University of Utah, Salt Lake, UT 84112, USA.
  • Ireland CM; Department of Medicinal Chemistry, University of Utah, Salt Lake, UT 84112, USA.
  • Bild AH; Department of Pharmacology and Toxicology, University of Utah, Salt Lake, UT 84112, USA.
  • Moos PJ; Department of Medical Oncology and Therapeutics Research, City of Hope, Monrovia, CA 91016, USA.
Mar Drugs ; 19(1)2021 Jan 18.
Article em En | MEDLINE | ID: mdl-33477536
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteróis / Neoplasias da Mama / Antineoplásicos Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esteróis / Neoplasias da Mama / Antineoplásicos Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article