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Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers

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 Lib...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831112/
https://www.ncbi.nlm.nih.gov/pubmed/33477536
http://dx.doi.org/10.3390/md19010041
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author 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.
author_facet 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.
author_sort El-Chaar, Nader N.
collection PubMed
description 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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spelling pubmed-78311122021-01-26 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. Mar Drugs Article 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. MDPI 2021-01-18 /pmc/articles/PMC7831112/ /pubmed/33477536 http://dx.doi.org/10.3390/md19010041 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
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.
Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers
title Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers
title_full Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers
title_fullStr Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers
title_full_unstemmed Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers
title_short Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers
title_sort topsentinol l trisulfate, a marine natural product that targets basal-like and claudin-low breast cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831112/
https://www.ncbi.nlm.nih.gov/pubmed/33477536
http://dx.doi.org/10.3390/md19010041
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