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	<title>Bee Propolis &#187; Egyptian propolis</title>
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		<title>Propolis and it’s role against tumor in mice</title>
		<link>http://www.beepropolis.info/scientific-papers/propolis-and-its-role-against-tumor-in-mice/</link>
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		<pubDate>Fri, 07 Aug 2009 15:14:53 +0000</pubDate>
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				<category><![CDATA[Scientific Papers]]></category>
		<category><![CDATA[Cancer]]></category>
		<category><![CDATA[Egyptian propolis]]></category>
		<category><![CDATA[tumor]]></category>

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		<description><![CDATA[Crude Egyptian propolis has a strong inhibitory activity against tumors. The anti-tumor mechanism may be mediated by preventing oxidative damage and induction of apoptosis.]]></description>
			<content:encoded><![CDATA[<h2>Summary of Research:</h2>
<p><strong>BACKGROUND:</strong> Propolis has numerous biologic activities including antibiotic, antifungal, antiviral and anti-inflammatory properties. The present work is aimed to study the effect of crude Egyptian propolis on tumor in mice induced by Ehrlich ascitis carcinoma (EAC) cell line.</p>
<h2>The Results</h2>
<p>The administration of propolis (160 mg/kg body weight), by gastric intubation 2 h before the intraperitoneal injection of EAC, effectively inhibited tumor growth and the proliferation of EAC.</p>
<p>The tumor volume was markedly reduced from 7+/-0.9 ml in EAC-infected mice to 1.6+/-0.95 ml in propolis-treated mice. Also, the lipid peroxide level which was 13.3+/-1.24 nmol malodialdehyde (MDA)/mg protein in EAC infected mice was significantly decreased to 3.3+/-2.1 nmol MDA/mg protein.</p>
<p>Reduced glutathione (GSH) and glutathione S-transferase (GST) concentrations were markedly increased in propolis-treated mice. This effect was associated with inhibition of cell cycle progression and induction of apoptosis.</p>
<p>Administration of propolis 2 h before injection of EAC arrested cells in G0/G1 phase and resulted in a decrease in the viability, DNA, total RNA and protein level of tumor cells.</p>
<h2>Conclusions</h2>
<p>Crude Egyptian propolis has a strong inhibitory activity against tumors. The anti-tumor mechanism may be mediated by preventing oxidative damage and induction of apoptosis.</p>
<p><strong>Authors:</strong> El-khawaga OA; Salem TA; Elshal MF<br />
Chemistry Department, Faculty of Science, Mansoura University, Mansoura City, Egypt. elkhawaga70s@mans.edu.eg</p>
<p><strong>Journal:</strong> Clinica chimica acta; international journal of clinical chemistry<br />
<strong>Issue:</strong> 2003; 338(1-2):11-6<br />
<strong>ISSN :</strong>0009-8981</p>
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