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.
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 |