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Abstract 4934: Detection of HBV-host junction DNA sequences in urine of patients with hepatocellular carcinoma
Journal article   Peer reviewed

Abstract 4934: Detection of HBV-host junction DNA sequences in urine of patients with hepatocellular carcinoma

Selena Lin, Evan Trauger, Benjamin Song, Ling Lan, Patrick Jongeneel, Emilie Thompson, Malcolm Hoffman, Surbhi Jain, Ting-Tsung Chang, Timothy Block, …
Cancer research (Chicago, Ill.), v 76(14_Supplement), pp 4934-4934
15 Jul 2016

Abstract

Hepatitis B virus
Human urine has been shown to contain DNA from circulation. In this study, we aim to provide unambiguous evidence that urine contains hepatocellular carcinoma (HCC)-derived DNA, and thus can be used for detecting HCC-associated DNA markers. We used novel hepatitis B virus (HBV)-host junction sequences (HBV-JSs), created by viral integration in the human genome, as unique markers to track the HBV-integrated DNA from tumor tissues to their corresponding urine samples. An HBV DR1-2 enriched Next-Generation sequencing (NGS) assay was developed to identify the major HBV-JSs in 15 HBV-HCC tissues. Upon validation of the major HBV-JSs by Sanger sequencing, a short-amplicon PCR assay tailed for each HBV-JS was developed to test the junctions existence in the corresponding urine DNA. 15 major HBV-JSs were identified by the HBV DR1-2 enriched NGS assay from 15 HBV related HCC (HBV-HCC) tissues, 13 of which were validated by Sanger sequencing. By using HBV-JS specific short-amplicon junction PCR assays, we detected and confirmed six of nine HBV-JSs for which there were matching urine samples. Urine contains detectable major HBV-JSs derived from HCC, and thus can be used for liquid biopsies to study not only the complexities of HBV-JS species during chronic HBV infection and carcinogenesis, but also other HCC-related DNA modifications for the early detection of HCC and disease management.

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Oncology
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