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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biomedical and Pharmacology Journal</journalTitle>
          <issn>0974-6242</issn>
            <publicationDate>2016-12-22</publicationDate>
    
        <volume>9</volume>
        <issue>3</issue>

 
    <startPage>919</startPage>
    <endPage>925</endPage>

	 
      <doi>10.13005/bpj/1030</doi>
        <publisherRecordId>10594</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Ethanol Extract of Annona Muricata. L Induces Liver Cancer Cell Apoptosis Through ROS Pathway</title>

    <authors>
	 


      <author>
       <name>Huali Yang</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Na Liu</name>


		
	<affiliationId>1</affiliationId>

      </author>
    

	 


      <author>
       <name>Shaochin Lee</name>

		
	<affiliationId>1</affiliationId>
      </author>
    

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">School of Life Sciences, Shanxi University, Taiyuan, Shanxi, PR China.</affiliationName>
    

		
		
		
		
		
	  </affiliationsList>






    <abstract language="eng">The study investigated the underlying molecular mechanisms of ethanol extract of<em> Annona muricata</em>. L induced liver cancer cell apoptosis. The anti-proliferative effect of ethanol extract of <em>Annona muricata</em>. L was evaluated by MTT assay. Flow cytometry was used to detect the cell cycle and apoptosis. TUNEL assay was used to confirm cell apoptosis. DCFH-DA fluorescent probe can detect the level of intracellular reactive oxygen species (ROS). Different concentrations of ethanol extract of <em>Annona muricata</em>. L leaves (0, 30, 60, 120, 240 µg/ml) were used to treat liver cancer HepG2 cells for 24h or 48h, the cell viability was inhibited in time- and dose-dependent manners. Ethanol extract of <em>Annona muricata</em>. L leaves increased the number of cells in the sub-G1 fraction in a dose-dependent manner. TUNEL assay confirmed that the extract caused apoptosis of the cancer cells. Further analysis revealed that the extract produced reactive oxygen species (ROS). Antioxidant N-acetylcysteine was able to inhibit the extract-triggered ROS production and apoptosis. In conclusion, our results suggest that the ethanol extract of <em>Annona muricata</em>. L leaves induces HepG2 cell apoptosis through ROS pathway.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol9no3/ethanol-extract-of-annona-muricata-l-induces-liver-cancer-cell-apoptosis-through-ros-pathway/</fullTextUrl>

<keywords language="eng">

      
        <keyword><em>Annona muricata</em>. L</keyword>
      

      
        <keyword> liver cancer cell</keyword>
      

      
        <keyword> apoptosis</keyword>
      

      
        <keyword> ROS</keyword>
      
</keywords>
  </record>
</records>