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Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers
Nader N El-Chaar1, Thomas E Smith2, Gajendra Shrestha1
1Department of Pharmacology and Toxicology, University of Utah, Salt Lake, UT 84112, USA.
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.
Insights
Researchers discovered topsentinol L trisulfate (TLT), a marine compound effective against aggressive basal-like/claudin-low breast cancers. TLT targets key signaling pathways, offering new therapeutic potential for difficult-to-treat cancers.
Area of Science:
- Marine natural products
- Cancer biology
- Drug discovery
Background:
- Basal-like and claudin-low (BL-CL) breast cancers have poor prognosis and limited treatment options.
- Novel therapeutic targets are urgently needed for these aggressive subtypes.
Purpose of the Study:
- To screen marine invertebrate compounds for specific activity against BL-CL breast cancers.
- To identify and characterize novel compounds targeting BL-CL breast cancer.
Main Methods:
- Screening of the Marine Invertebrate Compound Library (MICL).
- Biochemical assays to determine the mechanism of action of identified compounds.
- Validation using small molecule inhibitors of targeted pathways (AMPK, CHK1).
- Generation and application of a drug response gene-expression signature.
Main Results:
- Identification of topsentinol L trisulfate (TLT), a novel trisulfated sterol.
- TLT demonstrated increased efficacy against BL-CL breast cancer cell lines compared to luminal/HER2+.
- TLT inhibits AMP-activated protein kinase (AMPK) and checkpoint kinase 1 (CHK1) while promoting p38 activation.
- Gene-expression signature analysis identified breast and bladder cancers as most sensitive to TLT.
Conclusions:
- Topsentinol L trisulfate (TLT) is a promising novel compound for targeting basal-like/claudin-low breast cancers.
- Targeting AMPK and CHK1 pathways is crucial for BL-CL breast cancer treatment.
- TLT exhibits potential for treating other sensitive cancer types, including bladder cancer.
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