Evaluation of Circular RNA SMARCA5 as a Novel Biomarker for Hepatocellular Carcinoma

Bedair, Hanan M.; El-Banna, Elaf A; Ahmed, Elhamy A.; Elhelbawy, Mostafa G; Abdelfattah, Ahmed; Khalaf, Fatma A.; Abdel-Samiee, Mohamed; El Sharnoby, Amal

doi:10.31557/APJCP.2024.25.4.1411

Evaluation of Circular RNA SMARCA5 as a Novel Biomarker for Hepatocellular Carcinoma

Document Type : Research Articles

Authors

¹ Department of Clinical Pathology, National Liver Institute, Menoufia University, Shebin El-Kom, Egypt.

² Department of Hepatology and Gastroenterology, National Liver Institute, Menoufia University, Shebin El-Kom, Egypt.

³ Department of Clinical Biochemistry, National Liver Institute, Menoufia University, Shebin El-Kom, Egypt.

10.31557/APJCP.2024.25.4.1411

Abstract

Background: Hepatocellular carcinoma (HCC) is the fourth most prevalent type of cancer in Egypt and the sixth globally. Most patients with HCC are typically diagnosed during the advanced stages of the disease due to the absence of biomarkers for early detection. Consequently, these patients miss the optimal timeframe for receiving therapy. Objective: we aimed to assess the circular RNA SMARCA5 level and SMARCA5 mRNA gene expression as a potential biomarker for early detection of HCC. Methods: The present study utilized a case-control design comprising 159 participants. Participants were selected from both inpatient and outpatient hepatology and gastroenterology clinics at the National Liver Institute Hospital, Menoufia University. They were evenly distributed among three groups: Group I: 53 control subjects, Group II: 53 HCV cirrhotic patients, and Group III: 53 HCC patients. Tumor staging was done using BCLC staging system. Each patient underwent a thorough clinical examination, radiological examination, complete history taking, and serum Alpha-fetoprotein (AFP) assessment and detection of circular RNASMARCA5 and SMARCA5mRNA gene sutilizing quantitative real-time polymerase chain reaction. Results: Statistically substantial differences were observed in the examined groups in terms of AFP, SMARCA5, and CircSMARCA5 (P-value = 0.001, 0.001 & 0.001). CircSMARCA5 and SMARCA5mRNA were markedly down regulated in the HCC group compared to HCV cirrhotic patients and controls. ROC analysis for early HCC diagnosis demonstrated that the CircSMARCA5 area under the curve (AUC) at cut-off point 4.55 yielded a specificity of 83.8% and sensitivity of 91.7%. The AUC for AFP at a cut-off point of 515ng/ml yielded a specificity of 89.2% and a sensitivity of 91.3%. Conclusion: CircSMARCA5 has the potential to be a more sensitive predictor of HCC disease compared to AFP.

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