Topsentinol L Trisulfate, a Marine Natural Product That Targets Basal-like and Claudin-Low Breast Cancers.
Nader N El-ChaarThomas E SmithGajendra ShresthaStephen R PiccoloMary Kay HarperRyan M Van WagonerZhenyu LuAshlee R VenancioChris M IrelandAndrea H BildPhilip J MoosPublished in: Marine drugs (2021)
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.
Keyphrases
- protein kinase
- gene expression
- poor prognosis
- small molecule
- childhood cancer
- skeletal muscle
- dna methylation
- randomized controlled trial
- papillary thyroid
- long non coding rna
- newly diagnosed
- end stage renal disease
- climate change
- dna damage
- ejection fraction
- dna damage response
- young adults
- oxidative stress
- squamous cell
- tyrosine kinase
- muscle invasive bladder cancer
- breast cancer risk