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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Payame Noor University</PublisherName>
				<JournalTitle>Experimental animal Biology</JournalTitle>
				<Issn>2322-2387</Issn>
				<Volume>10</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>2021</Year>
					<Month>10</Month>
					<Day>23</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Antioxidant Effects of ‎C-Phycocyanin in Colon Cancer ‎Cell Lines invitro and invivo</ArticleTitle>
<VernacularTitle>Antioxidant Effects of ‎C-Phycocyanin in Colon Cancer ‎Cell Lines invitro and invivo</VernacularTitle>
			<FirstPage>21</FirstPage>
			<LastPage>30</LastPage>
			<ELocationID EIdType="pii">8157</ELocationID>
			
<ELocationID EIdType="doi">10.30473/eab.2021.58018.1821</ELocationID>
			
			<Language>FA</Language>
<AuthorList>
<Author>
					<FirstName>Leyla</FirstName>
					<LastName>Najafi</LastName>
<Affiliation>Ph.D., Biochemistry Department, Payame Noor University, Iran‎</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Fazilati</LastName>
<Affiliation>Professor of Biochemistry Department, Payame Noor ‎University, Iran‎</Affiliation>

</Author>
<Author>
					<FirstName>Hossein</FirstName>
					<LastName>Salavati</LastName>
<Affiliation>Associate Professor of Chemistry Department, Payame Noor ‎University, Iran‎</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2021</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</History>
		<Abstract>C-Phycocyanin has been demonstrated to have a series of pharmacological attributes without leading to toxicity. The aim of this study was to evaluate potential of anti-cancer and antioxidant C-PC on &lt;em&gt;CT-26&lt;/em&gt; and &lt;em&gt;HT-29&lt;/em&gt; cell lines &lt;em&gt;in vitro&lt;/em&gt; and in &lt;em&gt;Balb/c&lt;/em&gt; mice. The &lt;em&gt;CT-26&lt;/em&gt; and &lt;em&gt;HT-29&lt;/em&gt; cells were treated with various concentrations of C-PC extract (1-100&lt;em&gt;µg/ml&lt;/em&gt;) in 48hr. Antiproliferative effect was measured by morphological observations, &lt;em&gt;DAPI&lt;/em&gt; and &lt;em&gt;AO/PI&lt;/em&gt; Staining, &lt;em&gt;MTT&lt;/em&gt; assay, &lt;em&gt;fluorescence microscope&lt;/em&gt; and &lt;em&gt;Flow cytometry&lt;/em&gt; assays. Antioxidant effects of C-PC on &lt;em&gt;CT-26&lt;/em&gt; tumor cells transplanted in &lt;em&gt;Balb/c&lt;/em&gt; mice was also checked out &lt;em&gt;invivo&lt;/em&gt;. Male &lt;em&gt;Balb/c&lt;/em&gt; mice were tested in four groups.group1 was considered as control. Group 2 were fed by C-Phycocyanin (50&lt;em&gt;mg/kg&lt;/em&gt;) daily. In groups 2-4, cisplatin (3&lt;em&gt;mg/kg&lt;/em&gt;) was injected, and group 3 silymarin (100&lt;em&gt;mg/kg&lt;/em&gt;) was injected daily. Finally serum levels of &lt;em&gt;MDA&lt;/em&gt;, &lt;em&gt;TAC&lt;/em&gt;, and &lt;em&gt;Total Billirubin&lt;/em&gt;, &lt;em&gt;Total Protein&lt;/em&gt; and &lt;em&gt;Albumin&lt;/em&gt; and activities of &lt;em&gt;GPX&lt;/em&gt;, &lt;em&gt;Catalase&lt;/em&gt;, &lt;em&gt;SOD&lt;/em&gt;, &lt;em&gt;ALT&lt;/em&gt;, &lt;em&gt;AST&lt;/em&gt;, and &lt;em&gt;LDH&lt;/em&gt; were assayed. C-PC showed considerable anti-proliferative effect on &lt;em&gt;CT-26&lt;/em&gt; and &lt;em&gt;HT-29&lt;/em&gt; tumor cell lines with &lt;em&gt;IC50&lt;/em&gt; =47.4 &lt;em&gt;µg/ml&lt;/em&gt; and &lt;em&gt;IC50&lt;/em&gt;=49.4 &lt;em&gt;µg/ml&lt;/em&gt; respectively. In addition, C-PC because of its antioxidant potential, significantly (&lt;em&gt;P&lt;0/001&lt;/em&gt;), decreased &lt;em&gt;MDA&lt;/em&gt; and increased levels of liver antioxidant enzymes.</Abstract>
			<OtherAbstract Language="FA">C-Phycocyanin has been demonstrated to have a series of pharmacological attributes without leading to toxicity. The aim of this study was to evaluate potential of anti-cancer and antioxidant C-PC on &lt;em&gt;CT-26&lt;/em&gt; and &lt;em&gt;HT-29&lt;/em&gt; cell lines &lt;em&gt;in vitro&lt;/em&gt; and in &lt;em&gt;Balb/c&lt;/em&gt; mice. The &lt;em&gt;CT-26&lt;/em&gt; and &lt;em&gt;HT-29&lt;/em&gt; cells were treated with various concentrations of C-PC extract (1-100&lt;em&gt;µg/ml&lt;/em&gt;) in 48hr. Antiproliferative effect was measured by morphological observations, &lt;em&gt;DAPI&lt;/em&gt; and &lt;em&gt;AO/PI&lt;/em&gt; Staining, &lt;em&gt;MTT&lt;/em&gt; assay, &lt;em&gt;fluorescence microscope&lt;/em&gt; and &lt;em&gt;Flow cytometry&lt;/em&gt; assays. Antioxidant effects of C-PC on &lt;em&gt;CT-26&lt;/em&gt; tumor cells transplanted in &lt;em&gt;Balb/c&lt;/em&gt; mice was also checked out &lt;em&gt;invivo&lt;/em&gt;. Male &lt;em&gt;Balb/c&lt;/em&gt; mice were tested in four groups.group1 was considered as control. Group 2 were fed by C-Phycocyanin (50&lt;em&gt;mg/kg&lt;/em&gt;) daily. In groups 2-4, cisplatin (3&lt;em&gt;mg/kg&lt;/em&gt;) was injected, and group 3 silymarin (100&lt;em&gt;mg/kg&lt;/em&gt;) was injected daily. Finally serum levels of &lt;em&gt;MDA&lt;/em&gt;, &lt;em&gt;TAC&lt;/em&gt;, and &lt;em&gt;Total Billirubin&lt;/em&gt;, &lt;em&gt;Total Protein&lt;/em&gt; and &lt;em&gt;Albumin&lt;/em&gt; and activities of &lt;em&gt;GPX&lt;/em&gt;, &lt;em&gt;Catalase&lt;/em&gt;, &lt;em&gt;SOD&lt;/em&gt;, &lt;em&gt;ALT&lt;/em&gt;, &lt;em&gt;AST&lt;/em&gt;, and &lt;em&gt;LDH&lt;/em&gt; were assayed. C-PC showed considerable anti-proliferative effect on &lt;em&gt;CT-26&lt;/em&gt; and &lt;em&gt;HT-29&lt;/em&gt; tumor cell lines with &lt;em&gt;IC50&lt;/em&gt; =47.4 &lt;em&gt;µg/ml&lt;/em&gt; and &lt;em&gt;IC50&lt;/em&gt;=49.4 &lt;em&gt;µg/ml&lt;/em&gt; respectively. In addition, C-PC because of its antioxidant potential, significantly (&lt;em&gt;P&lt;0/001&lt;/em&gt;), decreased &lt;em&gt;MDA&lt;/em&gt; and increased levels of liver antioxidant enzymes.</OtherAbstract>
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			<Param Name="value">‎‏ ‏Mice</Param>
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			<Param Name="value">Phycocyanin</Param>
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<ArchiveCopySource DocType="pdf">https://eab.journals.pnu.ac.ir/article_8157_f6d6d3bfdc005bfbfd5362854d548147.pdf</ArchiveCopySource>
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