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Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice

The purpose of our study was to determine the effect of the combined action of phytochemicals on the early stages of skin tumorigenesis, i.e. initiation and promotion. We tested calcium D-glucarate (CG) given in the diet, while resveratrol (RES) and ursolic acid (UA) were applied topically. The 7,12...

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Autores principales: KOWALCZYK, MAGDALENA C., JUNCO, JACOB J., KOWALCZYK, PIOTR, TOLSTYKH, OLGA, HANAUSEK, MARGARET, SLAGA, THOMAS J., WALASZEK, ZBIGNIEW
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787890/
https://www.ncbi.nlm.nih.gov/pubmed/23835587
http://dx.doi.org/10.3892/ijo.2013.2005
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author KOWALCZYK, MAGDALENA C.
JUNCO, JACOB J.
KOWALCZYK, PIOTR
TOLSTYKH, OLGA
HANAUSEK, MARGARET
SLAGA, THOMAS J.
WALASZEK, ZBIGNIEW
author_facet KOWALCZYK, MAGDALENA C.
JUNCO, JACOB J.
KOWALCZYK, PIOTR
TOLSTYKH, OLGA
HANAUSEK, MARGARET
SLAGA, THOMAS J.
WALASZEK, ZBIGNIEW
author_sort KOWALCZYK, MAGDALENA C.
collection PubMed
description The purpose of our study was to determine the effect of the combined action of phytochemicals on the early stages of skin tumorigenesis, i.e. initiation and promotion. We tested calcium D-glucarate (CG) given in the diet, while resveratrol (RES) and ursolic acid (UA) were applied topically. The 7,12-dimethylbenz[a]anthracene (DMBA)-initiated, 12-O-tetradecanoylphorbol-13-acetate (TPA)-promoted multistage skin carcinogenesis model in SENCAR mice was used. Mice received one topical dose of DMBA, then after one month, two weekly doses of TPA for 14 weeks until sacrifice. RES or UA were applied 20 min prior to DMBA or TPA treatment and 2% dietary CG was given from 2 weeks prior to 2 weeks after the DMBA dose or continually beginning 2 weeks prior to the first dose of TPA. UA applied alone and in combination with CG during the promotion stage was the only inhibitor of tumor multiplicity and tumor incidence. A number of combinations reduced epidermal proliferation, but only UA and the combination UA+CG applied during promotion significantly reduced epidermal hyperplasia. DMBA/TPA application resulted in significant increases in c-jun and p50, which were reversed by a number of different treatments. DMBA/TPA treatment also strongly increased mRNA levels of inflammation markers COX-2 and IL-6. All anti-promotion treatments caused a marked decrease in COX-2 and IL-6 expression compared to the DMBA/TPA control. These results show that UA is a potent inhibitor of skin tumor promotion and inflammatory signaling and it may be useful in the prevention of skin cancer and other epithelial cancers in humans.
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spelling pubmed-37878902013-10-17 Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice KOWALCZYK, MAGDALENA C. JUNCO, JACOB J. KOWALCZYK, PIOTR TOLSTYKH, OLGA HANAUSEK, MARGARET SLAGA, THOMAS J. WALASZEK, ZBIGNIEW Int J Oncol Articles The purpose of our study was to determine the effect of the combined action of phytochemicals on the early stages of skin tumorigenesis, i.e. initiation and promotion. We tested calcium D-glucarate (CG) given in the diet, while resveratrol (RES) and ursolic acid (UA) were applied topically. The 7,12-dimethylbenz[a]anthracene (DMBA)-initiated, 12-O-tetradecanoylphorbol-13-acetate (TPA)-promoted multistage skin carcinogenesis model in SENCAR mice was used. Mice received one topical dose of DMBA, then after one month, two weekly doses of TPA for 14 weeks until sacrifice. RES or UA were applied 20 min prior to DMBA or TPA treatment and 2% dietary CG was given from 2 weeks prior to 2 weeks after the DMBA dose or continually beginning 2 weeks prior to the first dose of TPA. UA applied alone and in combination with CG during the promotion stage was the only inhibitor of tumor multiplicity and tumor incidence. A number of combinations reduced epidermal proliferation, but only UA and the combination UA+CG applied during promotion significantly reduced epidermal hyperplasia. DMBA/TPA application resulted in significant increases in c-jun and p50, which were reversed by a number of different treatments. DMBA/TPA treatment also strongly increased mRNA levels of inflammation markers COX-2 and IL-6. All anti-promotion treatments caused a marked decrease in COX-2 and IL-6 expression compared to the DMBA/TPA control. These results show that UA is a potent inhibitor of skin tumor promotion and inflammatory signaling and it may be useful in the prevention of skin cancer and other epithelial cancers in humans. D.A. Spandidos 2013-07-05 /pmc/articles/PMC3787890/ /pubmed/23835587 http://dx.doi.org/10.3892/ijo.2013.2005 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
KOWALCZYK, MAGDALENA C.
JUNCO, JACOB J.
KOWALCZYK, PIOTR
TOLSTYKH, OLGA
HANAUSEK, MARGARET
SLAGA, THOMAS J.
WALASZEK, ZBIGNIEW
Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice
title Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice
title_full Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice
title_fullStr Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice
title_full_unstemmed Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice
title_short Effects of combined phytochemicals on skin tumorigenesis in SENCAR mice
title_sort effects of combined phytochemicals on skin tumorigenesis in sencar mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3787890/
https://www.ncbi.nlm.nih.gov/pubmed/23835587
http://dx.doi.org/10.3892/ijo.2013.2005
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