Hepatocellular carcinoma
(HCC) ranks among the most common causes
of cancer-related deaths globally. The high incidence of HCC is largely
linked to chronic hepatitis virus infections, liver cirrhosis, and
exposure to carcinogenic substances. Egypt has one of the world’s
highest burdens of HCC, with liver cirrhosis from chronic hepatitis
C virus (HCV) infection as the primary risk factor. Malignant conversion
of cirrhosis to HCC is often fatal in part because adequate biomarkers
are not available for diagnosis of HCC in the early stage. Therefore,
there is a critical need for more effective biomarkers to detect HCC
at an early stage, when therapeutic intervention is more likely to
be successful. Multiomics integration has emerged as a powerful strategy
to uncover biomarkers and better understand the molecular underpinnings
of complex diseases such as HCC. This study summarizes findings from
multiple untargeted and targeted mass spectrometry-based analyses
of proteins, N-linked glycans, and metabolites performed on blood
samples from HCC cases and cirrhotic cohorts recruited in Egypt. Integrative
analysis using machine learning methods is performed to identify a
panel of multiomics features that differentiates HCC cases from the
high-risk population of cirrhotic patients with liver cirrhosis.