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  1. Article ; Online: Pro-Apoptotic and Anti-Angiogenesis Effects of Olive Leaf Extract on Spontaneous Mouse Mammary Tumor Model by Balancing Vascular Endothelial Growth Factor and Endostatin Levels.

    Milanizadeh, Sara / Reza Bigdeli, Mohammad

    Nutrition and cancer

    2019  Volume 71, Issue 8, Page(s) 1374–1381

    Abstract: It has been proven that olive associated products such as olive leaf extract (OLE) causes significant reduction in cancer cells viability and proliferation. Female BALB/c adult mice were divided into four groups. Three days prior to oral treatments, ... ...

    Abstract It has been proven that olive associated products such as olive leaf extract (OLE) causes significant reduction in cancer cells viability and proliferation. Female BALB/c adult mice were divided into four groups. Three days prior to oral treatments, tumors were transplanted. First group were treated with distilled water and other three groups were received, respectively, 75, 150, and 225 mg/kg/day of OLE for three weeks. For assessment of anti-angiogenesis and pro-apoptotic effect of OLE on tumor tissue, tumor volume, cell mitosis and apoptosis, and also vascular endothelial growth factor (VEGF) and endostatin levels were assessed. OLE treatment with 150 and 225 mg/kg/day lead to significant reduction in tumor volume and cell mitosis compared with the control group, while the same doses significantly increase tumor cell apoptosis. OLE treatment with 150 mg/kg/day increase endostatin levels, while the same dose did not significantly decrease VEGF levels. The VEGF level is significantly reduced by the treatment with OLE 225 mg/kg/day for three weeks. Although, further studies are needed to clarify anti-angiogenesis and anti-apoptotic mechanism of OLE, consumption of OLE polyphenols after tumor transplantation reduced spontaneous mouse mammary tumor growth.
    MeSH term(s) Animals ; Apoptosis ; Breast Neoplasms/drug therapy ; Breast Neoplasms/metabolism ; Disease Models, Animal ; Endostatins/metabolism ; Female ; Mice ; Mice, Inbred BALB C ; Neovascularization, Pathologic/drug therapy ; Olea/chemistry ; Plant Extracts/pharmacology ; Plant Leaves/chemistry ; Vascular Endothelial Growth Factor A/metabolism
    Chemical Substances Endostatins ; Plant Extracts ; Vascular Endothelial Growth Factor A
    Language English
    Publishing date 2019-05-10
    Publishing country United States
    Document type Journal Article
    ZDB-ID 424433-3
    ISSN 1532-7914 ; 0163-5581
    ISSN (online) 1532-7914
    ISSN 0163-5581
    DOI 10.1080/01635581.2019.1609054
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Pro-Apoptotic and Anti-Angiogenesis Effects of Olive Leaf Extract on Spontaneous Mouse Mammary Tumor Model by Balancing Vascular Endothelial Growth Factor and Endostatin Levels

    Milanizadeh, Sara / Reza Bigdeli, Mohammad

    Nutrition and cancer. 2019 Nov. 17, v. 71, no. 8

    2019  

    Abstract: It has been proven that olive associated products such as olive leaf extract (OLE) causes significant reduction in cancer cells viability and proliferation. Female BALB/c adult mice were divided into four groups. Three days prior to oral treatments, ... ...

    Abstract It has been proven that olive associated products such as olive leaf extract (OLE) causes significant reduction in cancer cells viability and proliferation. Female BALB/c adult mice were divided into four groups. Three days prior to oral treatments, tumors were transplanted. First group were treated with distilled water and other three groups were received, respectively, 75, 150, and 225 mg/kg/day of OLE for three weeks. For assessment of anti-angiogenesis and pro-apoptotic effect of OLE on tumor tissue, tumor volume, cell mitosis and apoptosis, and also vascular endothelial growth factor (VEGF) and endostatin levels were assessed. OLE treatment with 150 and 225 mg/kg/day lead to significant reduction in tumor volume and cell mitosis compared with the control group, while the same doses significantly increase tumor cell apoptosis. OLE treatment with 150 mg/kg/day increase endostatin levels, while the same dose did not significantly decrease VEGF levels. The VEGF level is significantly reduced by the treatment with OLE 225 mg/kg/day for three weeks. Although, further studies are needed to clarify anti-angiogenesis and anti-apoptotic mechanism of OLE, consumption of OLE polyphenols after tumor transplantation reduced spontaneous mouse mammary tumor growth.
    Keywords Olea europaea ; adults ; apoptosis ; females ; leaf extracts ; mammary neoplasms (animal) ; mice ; mitosis ; models ; neoplasm cells ; olives ; oral administration ; polyphenols ; vascular endothelial growth factors ; viability
    Language English
    Dates of publication 2019-1117
    Size p. 1374-1381.
    Publishing place Taylor & Francis
    Document type Article
    ZDB-ID 2025822-7
    ISSN 1532-7914 ; 0163-5581
    ISSN (online) 1532-7914
    ISSN 0163-5581
    DOI 10.1080/01635581.2019.1609054
    Database NAL-Catalogue (AGRICOLA)

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  3. Article ; Online: Sustained release of silibinin-loaded chitosan nanoparticle induced apoptosis in glioma cells.

    Alipour, Maryam / Reza Bigdeli, Mohammad / Aligholi, Hadi / Rasoulian, Bahram / Khaksarian, Mojtaba

    Journal of biomedical materials research. Part A

    2019  Volume 108, Issue 3, Page(s) 458–469

    Abstract: In this study, a chitosan nanoparticle formulation was synthesized for loading silibinin as a sustained-release drug system to evaluate its effects on apoptosis in C6 glioma cells. This synthesized nanoparticle was analyzed by measurement methods ... ...

    Abstract In this study, a chitosan nanoparticle formulation was synthesized for loading silibinin as a sustained-release drug system to evaluate its effects on apoptosis in C6 glioma cells. This synthesized nanoparticle was analyzed by measurement methods including Fourier transform infrared (FTIR), field emission-scanning electron microscopy (FE-SEM), dynamic light scattering (DLS), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The formation and amorphization of nanoparticle were confirmed by FTIR and XRD analysis, respectively. The mean diameter of silibinin-loaded chitosan nanoparticles (SCNP) was 50 ± 7 and 188.6 ± 0.17 nm by using FE-SEM and DLS, respectively. In addition, the positive zeta potential of nanoparticles was +11.5. Rhodamine-conjugated SCNP analysis showed the internalization of silibinin to C6 glioma cells. The cytotoxicity assay indicated that the nanoformulation of silibinin was toxic to C6 glioma cells. Although SCNP significantly increased the expression of the both apoptotic genes in C6 cells, Bax and caspase3, it did not have any significant effect on the level of the antiapoptotic gene, Bcl2. In contrast, SCNP did not have any toxic effect on H9C2 cells. In conclusion, the results of the current study indicated that SCNP can be considered as a sustained-release drug system for future cell-based therapeutic strategies.
    MeSH term(s) Animals ; Antineoplastic Agents, Phytogenic/administration & dosage ; Antineoplastic Agents, Phytogenic/pharmacology ; Apoptosis/drug effects ; Cell Line, Tumor ; Chitosan/chemistry ; Delayed-Action Preparations/chemistry ; Glioma/drug therapy ; Humans ; Nanoparticles/chemistry ; Rats ; Silybin/administration & dosage ; Silybin/pharmacology
    Chemical Substances Antineoplastic Agents, Phytogenic ; Delayed-Action Preparations ; Silybin (4RKY41TBTF) ; Chitosan (9012-76-4)
    Language English
    Publishing date 2019-11-11
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2099989-6
    ISSN 1552-4965 ; 1549-3296 ; 0021-9304
    ISSN (online) 1552-4965
    ISSN 1549-3296 ; 0021-9304
    DOI 10.1002/jbm.a.36827
    Database MEDical Literature Analysis and Retrieval System OnLINE

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