Abstract
OBJECTIVE
To examine the inhibitory effects of recombinant purified arresten on tumor formation.
METHODS
Purified arresten protein was incubated with human umbilical vein endothelial cells (HUVECs) and HeLa cells in vitro. The
effect on proliferation of HUVECs and HeLa cells was examined using 3-(4,5)-dimethylthiahiazo (-z-y1)-3,5-di-phenytetrazoliumromide
assay, and apoptosis of these cells monitored by flow cytometry. The effect on migration of HUVECs and HeLa cells was examined
by Boyden chamber. Twenty colon carcinoma-bearing C67BL/6 mice were used to investigate the antitumor effects of arresten
protein. The mice were randomly divided into arresten treatment group (n = 10) and control group (n = 10). The microvessel
densities of the tumors were measured by immunohistochemical staining with anti-CD31 monoclonal antibody.
RESULTS
Arresten inhibited the proliferation and migration of HUVECs in a dose-dependent manner while promoting apoptosis. However,
arresten had no significant effects on the proliferation and apoptosis of HeLa cells. The migration of HeLa cells was modestly
inhibited by arresten. The arresten treatment group of mice showed no weight loss or unusual behavior during the course of
treatment, and the tumor growth was significantly decreased; in contrast, the control group of mice exhibited rapidly growing
tumors and cachexia. A dramatically decreased microvessel density in tumor tissues was found in arresten-treated mice compared
with that in the control mice.
Links
Authors
Institution
Department of Health Toxicology, School of Public Health in Shanxi Medical University, Taiyuan 030001, China.
Source
Chinese medical sciences journal = Chung-kuo i hsüeh k'o hsüeh tsa chih / Chinese Academy of Medical Sciences 27:1 2012 Mar pg 11-7MeSH
AdultAnimals
Antineoplastic Agents
Apoptosis
Base Sequence
Cell Proliferation
Collagen Type IV
Female
HeLa Cells
Human Umbilical Vein Endothelial Cells
Humans
Mice
Mice, Inbred C57BL
Molecular Sequence Data
Neoplasms, Experimental
Pub Type(s)
Journal ArticleResearch Support, Non-U.S. Gov't
Language
eng
PubMed ID
22734208
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