Antineoplastic effect of pectic polysaccharides from green sweet pepper (Capsicum annuum) on mammary tumor cells in vivo and in vitro

被引:28
作者
Adami, Eliana Rezende [1 ]
Corso, Claudia Rita [1 ]
Turin-Oliveira, Natalia Mulinari [1 ]
Galindo, Claudia Martins [1 ]
Milani, Leticia [1 ]
Stipp, Maria Caroline [1 ]
do Nascimento, Georgia Erdmann [2 ]
Chequin, Andressa [3 ]
da Silva, Luisa Mota [4 ]
de Andrade, Sergio Faloni [4 ]
Dittrich, Rosangela Locatelli [5 ]
Queiroz-Telles, Jose Ederaldo [6 ]
Klassen, Giseli [3 ]
Ramos, Edneia A. S. [3 ]
Cordeiro, Lucimara M. C. [2 ]
Acco, Alexandra [1 ]
机构
[1] Univ Fed Parana, Dept Pharmacol, Curitiba, Parana, Brazil
[2] Univ Fed Parana, Dept Biochem & Mol Biol, Curitiba, Parana, Brazil
[3] Univ Fed Parana, Dept Basic Pathol, Curitiba, Parana, Brazil
[4] Univ Vale Itajai, Postgrad Program Pharmaceut Sci, Itajai, SC, Brazil
[5] Univ Fed Parana, Dept Vet Med, Curitiba, PR, Brazil
[6] Univ Fed Parana, Dept Med Pathol, Curitiba, PR, Brazil
关键词
Ehrlich solid tumor; Pectic polysaccharide; Green sweet pepper; VEGF; Mammary tumor cells; Interleukin-6; APOPTOSIS; ASSAY; BAX;
D O I
10.1016/j.carbpol.2018.08.071
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The present study investigated the antineoplastic effects of pectic polysaccharides that were extracted from green sweet pepper (Capsicum annuum [CAP]) in the Ehrlich carcinoma in mice and in human mammary tumor lineages. After the subcutaneous inoculation of 2 x 10(6) Ehrlich tumor cells, Female Swiss mice received 50, 100, or 150 mg/kg CAP or vehicle orally once daily or methotrexate (2.5 mg/kg, i.p., every 5 days) for 21 days. CAP dose-dependently reduced Ehrlich tumor growth. It also reduced the viability of MCF-7, MDA-MB-231, and MDA-MB-436 human mammary cell lineages. Treatment with CAP reduced the gene expression of vascular endothelial growth factor in vivo and in vitro, reduced vessel areas of the tumors, and induced necrosis in Ehrlich solid tumors. CAP treatment significantly increased Interleukin-6 in tumors. The antineoplastic effect of CAP appears to depend on the regulation of inflammation and angiogenesis. Further studies are encouraged to better understand the CAP potential for the treatment of breast tumors.
引用
收藏
页码:280 / 292
页数:13
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