Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
VEGA 1/0136/19; VEGA 1/0653/19; and 1/0753/17
Scientific Grant Agency of the Ministry of Education of the Slovak Republic
APVV-16-0021 and APVV-16-0446
Slovak Research and Development Agency
ITMS2014+: 313011V455
Open scientific community for modern interdisciplinary research in medicine (OPENMED)
NPRP 11S-1214-170101
National Priorities Research Program grant (NPRP 11S-1214-170101; awarded to Professor Dr. Dietrich Büsselberg, June 2019-Current) from the Qatar National Research Fund (QNRF, a member of Qatar Foundation).
PubMed
33375383
PubMed Central
PMC7795985
DOI
10.3390/ijms22010183
PII: ijms22010183
Knihovny.cz E-zdroje
- Klíčová slova
- MCF-7 cells, MDA-MB-231 cells, Rhus coriaria, angiogenesis, apoptosis, breast cancer, cancer stem cells, cell proliferation, epigenetics, mouse, rat, sumac,
- MeSH
- antitumorózní látky fytogenní farmakologie MeSH
- apoptóza MeSH
- buněčný cyklus MeSH
- lidé MeSH
- mikro RNA genetika MeSH
- myši inbrední BALB C MeSH
- myši nahé MeSH
- myši MeSH
- nádorové biomarkery genetika metabolismus MeSH
- nádorové buňky kultivované MeSH
- nádory prsu farmakoterapie metabolismus patologie MeSH
- potkani Sprague-Dawley MeSH
- proliferace buněk MeSH
- regulace genové exprese u nádorů účinky léků MeSH
- Rhus chemie MeSH
- rostlinné extrakty farmakologie MeSH
- xenogenní modely - testy antitumorózní aktivity MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antitumorózní látky fytogenní MeSH
- mikro RNA MeSH
- nádorové biomarkery MeSH
- rostlinné extrakty MeSH
Comprehensive scientific data provide evidence that isolated phytochemicals or whole plant foods may beneficially modify carcinogenesis. The aim of this study was to evaluate the oncostatic activities of Rhus coriaria L. (sumac) using animal models (rat and mouse), and cell lines of breast carcinoma. R. coriaria (as a powder) was administered through the diet at two concentrations (low dose: 0.1% (w/w) and high dose: 1 % (w/w)) for the duration of the experiment in a syngeneic 4T1 mouse and chemically-induced rat mammary carcinoma models. After autopsy, histopathological and molecular analyses of tumor samples in rodents were performed. Moreover, in vitro analyses using MCF-7 and MDA-MB-231 cells were conducted. The dominant metabolites present in tested R. coriaria methanolic extract were glycosides of gallic acid (possible gallotannins). In the mouse model, R. coriaria at a higher dose (1%) significantly decreased tumor volume by 27% when compared to controls. In addition, treated tumors showed significant dose-dependent decrease in mitotic activity index by 36.5% and 51% in comparison with the control group. In the chemoprevention study using rats, R. coriaria at a higher dose significantly reduced the tumor incidence by 20% and in lower dose non-significantly reduced tumor frequency by 29% when compared to controls. Evaluations of the mechanism of oncostatic action using valid clinical markers demonstrated several positive alterations in rat tumor cells after the treatment with R. coriaria. In this regard, histopathological analysis of treated tumor specimens showed robust dose-dependent decrease in the ratio of high-/low-grade carcinomas by 66% and 73% compared to controls. In treated rat carcinomas, we found significant caspase-3, Bax, and Bax/Bcl-2 expression increases; on the other side, a significant down-regulation of Bcl-2, Ki67, CD24, ALDH1, and EpCam expressions and MDA levels. When compared to control specimens, evaluation of epigenetic alterations in rat tumor cells in vivo showed significant dose-dependent decrease in lysine methylation status of H3K4m3 and H3K9m3 and dose-dependent increase in lysine acetylation in H4K16ac levels (H4K20m3 was not changed) in treated groups. However, only in lower dose of sumac were significant decreases in the expression of oncogenic miR210 and increase of tumor-suppressive miR145 (miR21, miR22, and miR155 were not changed) observed. Finally, only in lower sumac dose, significant decreases in methylation status of three out of five gene promoters-ATM, PTEN, and TIMP3 (PITX2 and RASSF1 promoters were not changed). In vitro evaluations using methanolic extract of R. coriaria showed significant anticancer efficacy in MCF-7 and MDA-MB-231 cells (using Resazurin, cell cycle, annexin V/PI, caspase-3/7, Bcl-2, PARP, and mitochondrial membrane potential analyses). In conclusion, sumac demonstrated significant oncostatic activities in rodent models of breast carcinoma that were validated by mechanistic studies in vivo and in vitro.
Biomedical Research Center Slovak Academy of Sciences 845 05 Bratislava Slovakia
Department of Medical Biology Faculty of Medicine P J Šafárik University 040 11 Kosice Slovakia
Department of Natural Drugs Faculty of Pharmacy Masaryk University 612 42 Brno Czech Republic
Department of Pathology St Elisabeth Oncology Institute 812 50 Bratislava Slovakia
Department of Pharmacology Faculty of Medicine P J Šafárik University 040 11 Košice Slovakia
Weill Cornell Medicine in Qatar Qatar Foundation Education City 24144 Doha Qatar
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Salvia officinalis L. exerts oncostatic effects in rodent and in vitro models of breast carcinoma
Anti-breast cancer effects of phytochemicals: primary, secondary, and tertiary care