The investigation of the antitumoral effect of Cornus mas L in mice with ehrlich solid tumor

AIM: Cornus mas L is commonly used due to its anti-inflammatory, anti-carcinogenic and anti-oxidant properties. In the study, the effects of C. mas L extract on a solid tumor were examined in the Ehrlich solid tumor model developed in Balb/C type mice. METHODS: Ehrlich acid tumor (EAT) cells (1x106 EAT cell) from the stock animal were injected subcutaneously (s.c.) through the nape of the mice. Treatment groups of solid tumor-induced animals received 100 mg/kg and 200 mg/kg of C. mas L extract intraperitoneally (i.p.) for 14 days. RESULTS: Tumor volumes and animal weights were found to be statistically significant compared to the control group (p < 0.05). AgNOR staining was performed in tumor tissues. Statistically significant differences were observed between the groups in terms of TAA/NA ratio (p < 0.05). Immunohistochemical and biochemical parameters were also evaluated. An estimation of tumor proliferation of the lung, liver, brain, kidney, testis and tumor antioxidant parameters viz. lipid peroxidation, reduced glutathione (GSH), glutathione S-transferase (GST), superoxide dismutase (SOD) and catalase (CAT) was made. CONCLUSIONS: Our study showed that the anti-tumor effect of C. mas L in assisted tumor development with EAT cells, was mediated by the enhancement of oxidative stress with multiple mechanisms (Tab. 6, Fig. 12, Ref. 38). Text in PDF www.elis.sk. © 2020, Comenius University.

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Eser Adı
(dc.title)
The investigation of the antitumoral effect of Cornus mas L in mice with ehrlich solid tumor
Yayın Türü
(dc.type)
Makale
Yazar/lar
(dc.contributor.author)
YILMAZ, Seher
Yazar/lar
(dc.contributor.author)
ALPA, Şerife
Yazar/lar
(dc.contributor.author)
GÖÇMEN, Ayşe Yeşim
Yazar/lar
(dc.contributor.author)
ÜLGER, Harun
Yazar/lar
(dc.contributor.author)
ARSLAN, Esra
Yazar/lar
(dc.contributor.author)
YAY, Arzu Hanım
Yazar/lar
(dc.contributor.author)
ERTEKİN, Tolga
Yazar/lar
(dc.contributor.author)
NİSARİ, Mehtap
Yazar/lar
(dc.contributor.author)
YALÇIN, Betül
DOI Numarası
(dc.identifier.doi)
10.4149/BLL_2020_004
Atıf Dizini
(dc.source.database)
Scopus
Konu Başlıkları
(dc.subject)
Ehrlich Solid Tumor
Konu Başlıkları
(dc.subject)
AgNOR
Konu Başlıkları
(dc.subject)
Anti-Tumor
Konu Başlıkları
(dc.subject)
Cornus Mas L
Yayıncı
(dc.publisher)
Comenius University
Yayın Tarihi
(dc.date.issued)
2020
Kayıt Giriş Tarihi
(dc.date.accessioned)
2020-08-07T12:49:39Z
Açık Erişim tarihi
(dc.date.available)
2020-08-07T12:49:39Z
Kaynak
(dc.source)
Bratislava Medical Journal
ISSN
(dc.identifier.issn)
00069248 (ISSN)
Özet
(dc.description.abstract)
AIM: Cornus mas L is commonly used due to its anti-inflammatory, anti-carcinogenic and anti-oxidant properties. In the study, the effects of C. mas L extract on a solid tumor were examined in the Ehrlich solid tumor model developed in Balb/C type mice. METHODS: Ehrlich acid tumor (EAT) cells (1x106 EAT cell) from the stock animal were injected subcutaneously (s.c.) through the nape of the mice. Treatment groups of solid tumor-induced animals received 100 mg/kg and 200 mg/kg of C. mas L extract intraperitoneally (i.p.) for 14 days. RESULTS: Tumor volumes and animal weights were found to be statistically significant compared to the control group (p < 0.05). AgNOR staining was performed in tumor tissues. Statistically significant differences were observed between the groups in terms of TAA/NA ratio (p < 0.05). Immunohistochemical and biochemical parameters were also evaluated. An estimation of tumor proliferation of the lung, liver, brain, kidney, testis and tumor antioxidant parameters viz. lipid peroxidation, reduced glutathione (GSH), glutathione S-transferase (GST), superoxide dismutase (SOD) and catalase (CAT) was made. CONCLUSIONS: Our study showed that the anti-tumor effect of C. mas L in assisted tumor development with EAT cells, was mediated by the enhancement of oxidative stress with multiple mechanisms (Tab. 6, Fig. 12, Ref. 38). Text in PDF www.elis.sk. © 2020, Comenius University.
Yayın Dili
(dc.language.iso)
eng
Tek Biçim Adres
(dc.identifier.uri)
http://hdl.handle.net/20.500.12498/2735
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