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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>2024-03-20</publicationDate>
    
        <volume>17</volume>
        <issue>1</issue>

 
    <startPage>469</startPage>
    <endPage>481</endPage>

	 
      <doi>10.13005/bpj/2875</doi>
        <publisherRecordId>56369</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Association of MTHFD1 G1958A, MTHFD1 T401C and CBS 844ins68bp with Breast Cancer in Jordan</title>

    <authors>
	 


      <author>
       <name>Samira Daw Ameigaal</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Almuthanna K. Alkaraki </name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	 


      <author>
       <name>May Fouad Sadiq </name>

		
	<affiliationId>2</affiliationId>
      </author>
    

	


	


	
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Department of Medical Laboratories, Higher Institute of Medical Sciences and Technology, Bani Waleed, Libya</affiliationName>
    

		
		<affiliationName affiliationId="2">Department of Biological Sciences, Faculty of Science, Yarmouk University, Irbid 21163, Jordan</affiliationName>
    
		
		
		
		
	  </affiliationsList>






    <abstract language="eng"><em>MTHFD1</em> and <em>CBS</em> genes have key roles in folate and homocysteine metabolism. Many studies reported an association between cancer pathogenesis and different functional SNPs of genes involved in the main folate metabolism and the transsulfuration pathway. The current population-based, case-control study examined the association between MTHFD1 G1958A, <em>MTHFD1</em> T401C, and the <em>CBS</em> 844ins68 insertion with breast cancer (BC) risk in Jordanian women. The studied population included 200  female BC subjects and age-matched female controls. The targeted genotypes <em>MTHFD1</em> G1958A and <em>MTHFD1</em> T401C were amplified via PCR followed by subsequent digestion with the proper restriction enzyme (PCR-RFLP), while the insertion/deletion of <em>CBS</em>844ins68bp was visualized and scored directly after gel electrophoresis. Results showed that the examined individual alleles and genotypes of <em>MTHFD</em> 1958A, <em>MTHFD1</em> 401C, and <em>CBS</em>844ins68bp <em>per se </em>were not associated with risk of BC compared with their wild-type genotypes and alleles.</abstract>

    <fullTextUrl format="html">https://biomedpharmajournal.org/vol17no1/association-of-mthfd1-g1958a-mthfd1-t401c-and-cbs-844ins68bp-with-breast-cancer-in-jordan/</fullTextUrl>

<keywords language="eng">

      
        <keyword>Breast cancer</keyword>
      

      
        <keyword> CBS 844ins68</keyword>
      

      
        <keyword> Folic acid</keyword>
      

      
        <keyword> Jordan</keyword>
      

      
        <keyword> MTHFD1 G1958A</keyword>
      

      
        <keyword> MTHFD1 T401C</keyword>
      
</keywords>
  </record>
</records>