Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma

<p dir="ltr">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 c...

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Main Author: Peter Kubatka (11008854) (author)
Other Authors: Martin Kello (7284827) (author), Karol Kajo (5926877) (author), Marek Samec (14727823) (author), Alena Liskova (11008851) (author), Karin Jasek (18877807) (author), Lenka Koklesova (18102994) (author), Tomas Kuruc (18877810) (author), Marian Adamkov (18877813) (author), Karel Smejkal (11912513) (author), Emil Svajdlenka (8624334) (author), Peter Solar (18877816) (author), Martin Pec (18877819) (author), Dietrich Büsselberg (11008857) (author), Vladimira Sadlonova (18877822) (author), Jan Mojzis (18877825) (author)
Published: 2020
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_version_ 1864513512388165632
author Peter Kubatka (11008854)
author2 Martin Kello (7284827)
Karol Kajo (5926877)
Marek Samec (14727823)
Alena Liskova (11008851)
Karin Jasek (18877807)
Lenka Koklesova (18102994)
Tomas Kuruc (18877810)
Marian Adamkov (18877813)
Karel Smejkal (11912513)
Emil Svajdlenka (8624334)
Peter Solar (18877816)
Martin Pec (18877819)
Dietrich Büsselberg (11008857)
Vladimira Sadlonova (18877822)
Jan Mojzis (18877825)
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author_facet Peter Kubatka (11008854)
Martin Kello (7284827)
Karol Kajo (5926877)
Marek Samec (14727823)
Alena Liskova (11008851)
Karin Jasek (18877807)
Lenka Koklesova (18102994)
Tomas Kuruc (18877810)
Marian Adamkov (18877813)
Karel Smejkal (11912513)
Emil Svajdlenka (8624334)
Peter Solar (18877816)
Martin Pec (18877819)
Dietrich Büsselberg (11008857)
Vladimira Sadlonova (18877822)
Jan Mojzis (18877825)
author_role author
dc.creator.none.fl_str_mv Peter Kubatka (11008854)
Martin Kello (7284827)
Karol Kajo (5926877)
Marek Samec (14727823)
Alena Liskova (11008851)
Karin Jasek (18877807)
Lenka Koklesova (18102994)
Tomas Kuruc (18877810)
Marian Adamkov (18877813)
Karel Smejkal (11912513)
Emil Svajdlenka (8624334)
Peter Solar (18877816)
Martin Pec (18877819)
Dietrich Büsselberg (11008857)
Vladimira Sadlonova (18877822)
Jan Mojzis (18877825)
dc.date.none.fl_str_mv 2020-12-26T06:00:00Z
dc.identifier.none.fl_str_mv 10.3390/ijms22010183
dc.relation.none.fl_str_mv https://figshare.com/articles/journal_contribution/Rhus_coriaria_L_Sumac_Demonstrates_Oncostatic_Activity_in_the_Therapeutic_and_Preventive_Model_of_Breast_Carcinoma/26095672
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Biomedical and clinical sciences
Medical biotechnology
Oncology and carcinogenesis
Pharmacology and pharmaceutical sciences
Health sciences
Traditional, complementary and integrative medicine
angiogenesis
apoptosis
breast cancer
cancer stem cells
cell proliferation
epigenetics
MCF-7 cells
MDA-MB-231 cells
mouse
rat
Rhus coriaria
sumac
dc.title.none.fl_str_mv Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
dc.type.none.fl_str_mv Text
Journal contribution
info:eu-repo/semantics/publishedVersion
text
contribution to journal
description <p dir="ltr">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.</p><h2>Other Information</h2><p dir="ltr">Published in: International Journal of Molecular Sciences<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3390/ijms22010183" target="_blank">https://dx.doi.org/10.3390/ijms22010183</a></p>
eu_rights_str_mv openAccess
id Manara2_b978179a81e4e5fa80fbb7cafb8ea5f1
identifier_str_mv 10.3390/ijms22010183
network_acronym_str Manara2
network_name_str Manara2
oai_identifier_str oai:figshare.com:article/26095672
publishDate 2020
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rights_invalid_str_mv CC BY 4.0
spelling Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast CarcinomaPeter Kubatka (11008854)Martin Kello (7284827)Karol Kajo (5926877)Marek Samec (14727823)Alena Liskova (11008851)Karin Jasek (18877807)Lenka Koklesova (18102994)Tomas Kuruc (18877810)Marian Adamkov (18877813)Karel Smejkal (11912513)Emil Svajdlenka (8624334)Peter Solar (18877816)Martin Pec (18877819)Dietrich Büsselberg (11008857)Vladimira Sadlonova (18877822)Jan Mojzis (18877825)Biomedical and clinical sciencesMedical biotechnologyOncology and carcinogenesisPharmacology and pharmaceutical sciencesHealth sciencesTraditional, complementary and integrative medicineangiogenesisapoptosisbreast cancercancer stem cellscell proliferationepigeneticsMCF-7 cellsMDA-MB-231 cellsmouseratRhus coriariasumac<p dir="ltr">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.</p><h2>Other Information</h2><p dir="ltr">Published in: International Journal of Molecular Sciences<br>License: <a href="https://creativecommons.org/licenses/by/4.0/" target="_blank">https://creativecommons.org/licenses/by/4.0/</a><br>See article on publisher's website: <a href="https://dx.doi.org/10.3390/ijms22010183" target="_blank">https://dx.doi.org/10.3390/ijms22010183</a></p>2020-12-26T06:00:00ZTextJournal contributioninfo:eu-repo/semantics/publishedVersiontextcontribution to journal10.3390/ijms22010183https://figshare.com/articles/journal_contribution/Rhus_coriaria_L_Sumac_Demonstrates_Oncostatic_Activity_in_the_Therapeutic_and_Preventive_Model_of_Breast_Carcinoma/26095672CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/260956722020-12-26T06:00:00Z
spellingShingle Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
Peter Kubatka (11008854)
Biomedical and clinical sciences
Medical biotechnology
Oncology and carcinogenesis
Pharmacology and pharmaceutical sciences
Health sciences
Traditional, complementary and integrative medicine
angiogenesis
apoptosis
breast cancer
cancer stem cells
cell proliferation
epigenetics
MCF-7 cells
MDA-MB-231 cells
mouse
rat
Rhus coriaria
sumac
status_str publishedVersion
title Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
title_full Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
title_fullStr Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
title_full_unstemmed Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
title_short Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
title_sort Rhus coriaria L. (Sumac) Demonstrates Oncostatic Activity in the Therapeutic and Preventive Model of Breast Carcinoma
topic Biomedical and clinical sciences
Medical biotechnology
Oncology and carcinogenesis
Pharmacology and pharmaceutical sciences
Health sciences
Traditional, complementary and integrative medicine
angiogenesis
apoptosis
breast cancer
cancer stem cells
cell proliferation
epigenetics
MCF-7 cells
MDA-MB-231 cells
mouse
rat
Rhus coriaria
sumac