AI Article Synopsis

  • Hepatocellular carcinoma (HCC) is a challenging and deadly cancer with a high recurrence rate, making early diagnosis difficult.
  • This study investigates the long non-coding RNA DUXAP8 and its associated protein-coding genes (PCGs) to evaluate their potential as diagnostic and prognostic biomarkers for HCC using data from 370 patients.
  • The results revealed that DUXAP8 and specific PCGs have significant implications for diagnosis and prognosis, leading to a risk score model and identifying potential therapeutic drugs like cinchonine, bumetanide, and amiprilose.

Article Abstract

Hepatocellular carcinoma (HCC) is a lethal malignancy worldwide that is difficult to diagnose during the early stages and its tumors are recurrent. Long non-coding RNAs (lncRNAs) have increasingly been associated with tumor biomarkers for diagnosis and prognosis. This study attempts to explore the potential clinical significance of lncRNA DUXAP8 and its co-expression related protein coding genes (PCGs) for HCC. Data from a total of 370 HCC patients from The Cancer Genome Atlas were utilized for the analysis. DUXAP8 and its top 10 PCGs were explored for their diagnostic and prognostic implications for HCC. A risk score model and nomogram were constructed for prognosis prediction using prognosis-related genes and DUXAP8. Molecular mechanisms of DUXAP8 and its PCGs involved in HCC initiation and progression were investigated. Then, potential target drugs were identified using genome-wide DUXAP8-related differentially expressed genes in a Connectivity Map database. The top 10 PCGs were identified as: , , , , , , , , MALRD1, and . Diagnostic analysis indicated that DUXAP8, , , and show diagnostic implications (all area under curves ≥0.7, p≤0.05). Prognostic analysis indicated that DUXAP8 and had prognostic implications for HCC (adjusted p=0.014 and 0.008, respectively). The risk score model and nomogram showed an advantage for prognosis prediction. A total of 3 target drugs were determined: cinchonine, bumetanide and amiprilose and they may serve as potential therapeutic targets for HCC. Functioning as an oncogene, DUXAP8 is overexpressed in tumor tissue and may serve as both a diagnostic and prognosis biomarker for HCC. , , and maybe potential diagnostic biomarkers and may also be potentially prognostic biomarkers for HCC.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477403PMC
http://dx.doi.org/10.7150/jca.47902DOI Listing

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