Liquid biopsy using cell-free DNA in the early diagnosis of hepatocellular carcinoma.

Invest New Drugs

Department of Hepatobiliary and Pancreatic Surgery, General Surgery Center, The First Hospital of Jilin University, 71 Xinmin Street, Chaoyang District, Changchun, 130000, Jilin, China.

Published: June 2023

AI Article Synopsis

  • Hepatocellular carcinoma (HCC) is a major cancer-related cause of death globally, particularly in China, with early-stage detection significantly improving patient outcomes.
  • Traditional screening methods like ultrasound, CT, and serum AFP have limitations in diagnosing HCC at early stages due to low sensitivity.
  • Liquid biopsy, which involves analyzing cell-free DNA (cfDNA) and circulating tumor DNA (ctDNA) from blood, has emerged as a promising, noninvasive approach for the early detection of HCC and is the focus of recent research advancements.

Article Abstract

Hepatocellular carcinoma ranks fourth in cancer-related causes of death worldwide and second in China. Patients with hepatocellular carcinoma (HCC) at the early stage have a better prognosis compared to HCC patients at the late stage. Therefore, early screening for HCC is critical for clinical treatment decisions and improving the prognosis of patients. Ultrasound (US), computed tomography (CT), and serum alpha fetoprotein (AFP) have been used to screen HCC, but HCC is still difficult to be diagnosed in the early stage due to the low sensitivity of the above methods. It is urgent to find a method with high sensitivity and specificity for the early diagnosis of HCC. Liquid biopsy is a noninvasive detection method using blood or other bodily fluids. Cell-free DNA (cfDNA) and circulating tumor DNA (ctDNA) are important biomarkers for liquid biopsy. Recently, HCC screening methods using the application of cfDNA and ctDNA have become the hot spot of early HCC diagnostics. In this mini review, we summarize the latest research progress of liquid biopsy based on blood cfDNA in early screening of HCC.

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Source
http://dx.doi.org/10.1007/s10637-023-01363-6DOI Listing

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