Saltar al contenido
Merck

mTOR inhibitors counteract tamoxifen-induced activation of breast cancer stem cells.

Cancer letters (2015-07-26)
Govindasamy-Muralidharan Karthik, Ran Ma, John Lövrot, Lorand Levente Kis, Claes Lindh, Lennart Blomquist, Irma Fredriksson, Jonas Bergh, Johan Hartman
RESUMEN

Breast cancer cells with stem cell characteristics (CSC) are a distinct cell population with phenotypic similarities to mammary stem cells. CSCs are important drivers of tumorigenesis and the metastatic process. Tamoxifen is the most widely used hormonal therapy for estrogen receptor (ER) positive cancers. In our study, tamoxifen was effective in reducing proliferation of ER + adherent cancer cells, but not their CSC population. We isolated, expanded and incubated CSC from seven breast cancers with or without tamoxifen. By genome-wide transcriptional analysis we identified tamoxifen-induced transcriptional pathways associated with ribosomal biogenesis and mRNA translation, both regulated by the mTOR-pathway. We observed induction of the key mTOR downstream targets S6K1, S6RP and 4E-BP1 in-patient derived CSCs by tamoxifen on protein level. Using the mTOR inhibitors rapamycin, everolimus and PF-04691502 (a dual PI3K/mTOR inhibitor) and in combination with tamoxifen, significant reduction in mammosphere formation was observed. Hence, we suggest that the CSC population play a significant role during endocrine resistance through activity of the mTOR pathway. In addition, tamoxifen further stimulates the mTOR-pathway but can be antagonized using mTOR-inhibitors.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
Tamoxifeno, ≥99%
Sigma-Aldrich
4-hidroxitamoxifeno, ≥70% Z isomer (remainder primarily E-isomer)
Sigma-Aldrich
DAPI, for nucleic acid staining
Sigma-Aldrich
Fenol solution, Equilibrated with 10 mM Tris HCl, pH 8.0, 1 mM EDTA, BioReagent, for molecular biology
Sigma-Aldrich
Fenol solution, BioReagent, Saturated with 0.01 M citrate buffer, pH 4.3 ± 0.2, for molecular biology
Sigma-Aldrich
Fenol, ≥99%
Sigma-Aldrich
Fenol, puriss. p.a., ACS reagent, reag. Ph. Eur., 99.0-100.5%
Sigma-Aldrich
Rapamycin, Ready Made Solution, 2.5 mg/mL in DMSO (2.74 mM), from Streptomyces hygroscopicus
Sigma-Aldrich
Fenol solution, ≥89.0%
Sigma-Aldrich
Fenol, natural, 97%, FG
Sigma-Aldrich
Fenol, for molecular biology
Sigma-Aldrich
Fenol, BioUltra, for molecular biology, TE-saturated, ~73% (T)
Sigma-Aldrich
Fenol, BioXtra, ≥99.5% (GC)
Sigma-Aldrich
Fenol, puriss., meets analytical specification of Ph. Eur., BP, USP, ≥99.5% (GC), crystalline (detached)
Sigma-Aldrich
Fenol, contains hypophosphorous as stabilizer, loose crystals, ACS reagent, ≥99.0%
Sigma-Aldrich
Bicinchoninic acid disodium salt hydrate, ≥98% (HPLC)
Sigma-Aldrich
Fenol, unstabilized, ReagentPlus®, ≥99%
Sigma-Aldrich
Fenol, ≥96.0% (calc. on dry substance, T)
Sigma-Aldrich
Fenol, puriss., meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (GC)
Sigma-Aldrich
Fenol, unstabilized, purified by redistillation, ≥99%
Sigma-Aldrich
ALDH2 human, recombinant, expressed in E. coli, ≥90% (SDS-PAGE)
Sigma-Aldrich
Epiregulin human, recombinant, expressed in E. coli, ≥98% (SDS-PAGE), ≥98% (HPLC), suitable for cell culture
Sigma-Aldrich
MISSION® esiRNA, targeting human ESR1
Sigma-Aldrich
MISSION® esiRNA, targeting human ALDH2
Sigma-Aldrich
MISSION® esiRNA, targeting human EREG
Sigma-Aldrich
MISSION® esiRNA, targeting human DBI
Sigma-Aldrich
MISSION® esiRNA, targeting human HPS1