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<ArticleSet>
<Article>
<Journal>
				<PublisherName>West Asia Organization for Cancer Prevention (WAOCP), APOCP's West Asia Chapter.</PublisherName>
				<JournalTitle>Asian Pacific Journal of Cancer Prevention</JournalTitle>
				<Issn>1513-7368</Issn>
				<Volume>16</Volume>
				<Issue>15</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>12</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Mechanism of Chemoprevention against Colon Cancer Cells Using Combined Gelam Honey and Ginger Extract via mTOR and Wnt/β-catenin Pathways</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>6549</FirstPage>
			<LastPage>6556</LastPage>
			<ELocationID EIdType="pii">31440</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>1970</Year>
					<Month>01</Month>
					<Day>01</Day>
				</PubDate>
			</History>
		<Abstract>The PI3K-Akt-mTOR, Wnt/β-catenin and apoptosis signaling pathways have been shown to be involvedin genesis of colorectal cancer (CRC) . The aim of this study was to elucidate whether combination of Gelamhoney and ginger might have chemopreventive properties in HT29 colon cancer cells by modulating the mTOR,Wnt/β-catenin and apoptosis signaling pathways. Treatment with Gelam honey and ginger reduced the viabilityof the HT29 cells dose dependently with IC50 values of 88 mg/ml and 2.15 mg/ml respectively, their while thecombined treatment of 2 mg/ml of ginger with 31 mg/ml of Gelam honey inhibited growth of most HT29 cells.Gelam honey, ginger and combination induced apoptosis in a dose dependent manner with the combinedtreatment exhibiting the highest apoptosis rate. The combined treatment downregulated the gene expressions ofAkt, mTOR, Raptor, Rictor, β-catenin, Gsk3β, Tcf4 and cyclin D1 while cytochrome C and caspase 3 genes wereshown to be upregulated. In conclusion, the combination of Gelam honey and ginger may serve as a potentialtherapy in the treatment of colorectal cancer through inhibiton of mTOR, Wnt/β catenin signaling pathwaysand induction of apoptosis pathway.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">mTOR</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Wnt/β catenin</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Apoptosis</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Combination</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">HT29 colon cancer cells</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.waocp.org/article_31440_74e308f67a92e0a03f2ecbe222fe09d0.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
