AI Article Synopsis

  • The study explores the use of tumor-associated antigens (TAAs) as early diagnostic tools for hepatocellular carcinoma (HCC), specifically focusing on Hispanic patients who may have unique risk factors.
  • Researchers identified four significant anti-TAA autoantibodies—DNMT3A, p16, Hsp60, and HSPA5—that showed higher levels in the serum of Hispanic HCC patients, with a combined testing approach increasing diagnostic sensitivity to 75%.
  • Findings suggest that these autoantibodies, particularly DNMT3A and HSP60, could serve as valuable diagnostic biomarkers specifically for Hispanic HCC patients, indicating a potentially distinct profile in this demographic.

Article Abstract

Background: Tumor-associated antigens (TAAs) have been investigated for many years as potential early diagnosis tools, especially for hepatocellular carcinoma (HCC). Nonetheless, very few studies have focused on the Hispanic HCC group that may be associated with distinct etiological risk factors. In the present study, we investigated novel anti-TAA autoantibodies as diagnostic biomarkers for Hispanic HCC patients.

Methods: Novel TAA targets were identified by the serological proteome analysis (SERPA) and from differentially expressed HCC driver genes via bioinformatics. The autoantibody levels were validated by enzyme-linked immunosorbent assay (ELISA).

Results: Among 19 potential TAA targets, 4 anti-TAA autoantibodies were investigated as potential diagnostic biomarkers with significantly high levels in Hispanic HCC sera, including DNA methyltransferase 3A (DNMT3A), p16, Hear shock protein 60 (Hsp60), and Heat shock protein A5 (HSPA5). The area under the ROC curve (AUC) value of the single autoantibodies varies from 0.7505 to 0.8885. After combining all 4 autoantibodies, the sensitivity of the autoantibody panel increased to 75% compared to the single one with the highest value of 45.8%. In a separate analysis of the Asian cohort, autoantibodies against HSPA5 and p16 showed significantly elevated levels in HCC compared to normal healthy controls, but not for DNMT3A or HSP60.

Conclusion: Anti-DNMT3A, p16, HSPA5, and HSP60 autoantibodies have the potential to be diagnostic biomarkers for Hispanic HCC patients, of which DNMT3A and HSP60 might be exclusive for Hispanic HCC diagnosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600682PMC
http://dx.doi.org/10.3390/cells11203227DOI Listing

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