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P06.08-YI


          EFFECT OF RECK GENE POLYMORPHISMS ON
          HEPATOCELLULAR CARCINOMA SUSCEPTIBILITY AND
          PROGRESSION IN EGYPTIAN PATIENTS


          Ahmed M. El-Sayed Ahmed El Nakib , Sally A. AbdEL Aziz 2
                                         * 1
                                               2
          1 Tropical Medicine, Mansoura University Hospitals,  Medical Biochemistry Dept., Mansoura
          Faculty of Medicine, Mansoura, Egypt
          Corresponding author’s email: el_naqueeb@yahoo.com


          Introduction: Hepatocellular carcinoma (HCC) is the fifth most common cause of
          cancer worldwide. In Egypt, HCC was reported to account for about 4.7% of chronic liver
          disease (CLD) patients. The reversion-inducing-cysteine-rich protein with Kazal motifs
          (RECK) gene is a transformation suppressor gene against activated ras oncogenes. RECK
          gene may play a role in carcinogenesis and metastasis.

          Aims: To analyze the association between RECK gene single nucleotide polymorphisms
          (SNPs) and hepatocellular carcinoma susceptibility and progression among the Egyptian  ePOSTER ABSTRACTS
          patients.

          Material  and  Methods:  RECK  gene  rs16932912  SNP  and  rs11788747  SNP  were
          estimated using real-time PCR technique in 100 adult Egyptian patients with HCC ( 50
          patients have tumor size > 4 cm and 50patients with tumor size< 4 cm and 200 healthy
          control subjects

          Results: Rs16932912 polymorphism on HCC:
          There was significant decrease in the frequency of the homozygous GG genotype of
          rs16932912 polymorphism in studied HCC cases < 4cm as compared to that of control
          group. There was non-significant difference in the frequency of the homozygous GG
          genotype, homozygous mutant AA genotype, heterozygous mutant AG genotype and the
          risk value of the (AG+AA) genotype in studied HCC cases with tumor size > 4 cm as
          compared to that of control group.
          Rs11788747polymorphism on HCC:
          There was non-significant difference in the frequency of the heterozygous mutant AG
          genotype, homozygous AA genotype, homozygous mutant GG genotype and the risk value
          of (AG+AA) genotype for patients with HCC tumor size size > 4 cm and tumor size < 4
          cm as compared to that of control group.

          EASL HCC Summit  •  Geneva, Switzerland  •  2-5 February, 2017  237
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