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Epoxylathyrane Derivatives as MDR-Selective Compounds for Disabling Multidrug Resistance in Cancer

Reis, Mariana Alves (författare)
Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal.
Matos, Ana M. (författare)
Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal
Duarte, Noélia (författare)
Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal
visa fler...
Ahmed, Omar Bauomy (författare)
Univ Hosp Charite, Inst Pathol, Berlin, Germany
Ferreira, Ricardo J., PhD, 1980- (författare)
Uppsala universitet,Molekylär biofysik,Science for Life Laboratory, SciLifeLab,Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal
Lage, Hermann (författare)
Univ Hosp Charite, Inst Pathol, Berlin, Germany
Ferreira, Maria-José U. (författare)
Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal
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Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal Univ Lisbon, Fac Pharm, Res Inst Med iMed ULisboa, Lisbon, Portugal (creator_code:org_t)
2020-05-08
2020
Engelska.
Ingår i: Frontiers in Pharmacology. - : Frontiers Media SA. - 1663-9812. ; 11
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Multidrug resistance (MDR) has been regarded as one of the major hurdles for the successful outcome of cancer chemotherapy. The collateral sensitivity (CS) effect is one the most auspicious anti-MDR strategies. Epoxylathyrane derivatives 1-16 were obtained by derivatization of the macrocyclic diterpene epoxyboetirane A (17), a lathyrane-type macrocyclic diterpene isolated from Euphorbia boetica. Some of these compounds were found to strongly modulate P-glycoprotein (P-gp/ABCB1) efflux.Purpose: The main goal was to develop lathyrane-type macrocyclic diterpenes with improved MDR-modifying activity, by targeting more than one anti-MDR mechanism.Study design/methods: In this study, the potential CS effect of compounds 1-16 was evaluated against gastric (EPG85-257), pancreatic (EPP85-181), and colon (HT-29) human cancer cells and their drug-resistant counterparts, respectively selected against mitoxantrone (EPG85-257RNOV; EPP85-181RNOV; HT-RNOV) or daunorubicin (EPG85-257RDB; EPP85-181RDB; HT-RDB). The most promising compounds (8, 15, and 16) were investigated as apoptosis inducers, using the assays annexin V/PI and active caspase-3.Results: The compounds were more effective against the resistant gastric cell lines, being the CS effect more significant in EPG85-257RDB cells. Taking together the IC50 values and the CS effect, compounds 8, 15, and 16 exhibited the best results. Epoxyboetirane P (8), with the strongest MDR-selective antiproliferative activity against gastric carcinoma EPG85-257RDB cells (IC50 of 0.72 mu M), being 10-fold more active against this resistant subline than in sensitive gastric carcinoma cells. The CS effect elicited by compounds 15 and 16 appeared to be by inducing apoptosis via caspase-3 activation. Structure-activity relationships of the compounds were additionally obtained through regression models to clarify the structural determinants associated to the CS effect.Conclusions: This study reinforces the importance of lathyrane-type diterpenes as lead molecules for the research of MDR-modifying agents.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmaceutiska vetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmaceutical Sciences (hsv//eng)

Nyckelord

multidrug resistance
collateral sensitivity
apoptosis
Euphorbia
macrocyclic diterpenes
lathyrane
regression models

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