Gecko Crude Peptides Induce Apoptosis in Human Liver Carcinoma Cells In Vitro and Exert Antitumor Activity in a Mouse Ascites H22 Xenograft Model. (3rd October 2012)
- Record Type:
- Journal Article
- Title:
- Gecko Crude Peptides Induce Apoptosis in Human Liver Carcinoma Cells In Vitro and Exert Antitumor Activity in a Mouse Ascites H22 Xenograft Model. (3rd October 2012)
- Main Title:
- Gecko Crude Peptides Induce Apoptosis in Human Liver Carcinoma Cells In Vitro and Exert Antitumor Activity in a Mouse Ascites H22 Xenograft Model
- Authors:
- Song, Ying
Wang, Jian-Gang
Li, Rui-Fang
Li, Yan
Cui, Zhao-Chu
Duan, Leng-Xin
Lu, Fei - Other Names:
- Husain Kazim Academic Editor.
- Abstract:
- Abstract : Aim . To investigate the anti-tumor effects and mechanisms of gecko crude peptides (GCPs) in vitro and in vivo . Methods . 3-(4, 5)-dimethylthiahiazo (-z-y1)-3, 5-di-phenytetrazoliumromide (MTT) assay was applied to measure the effects of GCPs on the HepG2 cell viability. Fluorescence morphology was used to identify apoptotic cells. A xenograft H22 liver cancer model was established in Kunming mice. The tumor-bearing mice were treated with daily intraperitoneal injections of normal saline (NS group) or GCPs (80, 40 or 20 mg/kg) for 10 days, or once per two days with 2 mg/kg doxorubicin (ADR group;n = 10 each). Serum tumor necrosis factor (TNF- α ) and interleukin (IL)-6 were quantified using ELISA assay. Results . GCPs significantly inhibited the growth of HepG2 cells and induced typical apoptotic morphological features through increasing bcl-2/bax ratio in a dose- and time-dependent manner in vitro . The tumor weights of the ADR group, GCPs (H) group, GCPs (M) group, GCPs (L) group were smaller compared to the NS group. While the white blood cell count, thymus index, spleen index were higher in the high dose GCPs group than the NS group (P < 0.05 ), the VEGF expression in tumor tissue and serum TNF- α and IL-6 levels in the GCPs groups were lower than the NS group (P < 0.05 ).
- Is Part Of:
- Journal of biomedicine and biotechnology. Volume 2012(2012)
- Journal:
- Journal of biomedicine and biotechnology
- Issue:
- Volume 2012(2012)
- Issue Display:
- Volume 2012, Issue 2012 (2012)
- Year:
- 2012
- Volume:
- 2012
- Issue:
- 2012
- Issue Sort Value:
- 2012-2012-2012-0000
- Page Start:
- Page End:
- Publication Date:
- 2012-10-03
- Subjects:
- Medicine -- Periodicals
Biology -- Periodicals
Biotechnology -- Periodicals
Medicine
Biology
Biotechnology
Médecine
Biologie
Biotechnologie
Biology
Biotechnology
Medicine
Biotechnology
Biomedicine
Electronic journals
Periodical
Periodicals
Electronic journals
610 - Journal URLs:
- https://www.hindawi.com/journals/jbb/ ↗
- DOI:
- 10.1155/2012/743573 ↗
- Languages:
- English
- ISSNs:
- 1110-7243
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library HMNTS - ELD Digital store
- Ingest File:
- 10369.xml