4.7 Article

The Landscape of Aberrant Alternative Splicing Events in Steatotic Liver Graft Post Transplantation via Transcriptome-Wide Analysis

Journal

Publisher

MDPI
DOI: 10.3390/ijms24098216

Keywords

liver transplantation using steatotic graft; tumor recurrence; alternative splicing events; metabolism and immune cells; cancer hallmarks

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The application of steatotic liver graft has been increased due to donor shortage and prevalence of non-alcoholic fatty liver disease. However, steatotic livers are vulnerable to inflammatory injury, which may lead to cancer recurrence. This study identified differential alternative splicing events (ASEs) in steatotic liver grafts and their association with tumor recurrence. The differential ASEs were associated with HCC patients' survival and were enriched in metabolic pathways and immune cell distribution. The cancer hallmarks were also enriched in steatotic liver grafts and linked to differential ASEs. This work provides new insights into the relationship between steatotic liver graft injury and tumor recurrence, as well as potential markers for prognosis and therapy.
The application of steatotic liver graft has been increased significantly due to the severe donor shortage and prevalence of non-alcoholic fatty liver disease. However, steatotic donor livers are vulnerable to acute phase inflammatory injury, which may result in cancer recurrence. Alternative splicing events (ASEs) are critical for diverse transcriptional variants in hepatocellular carcinoma (HCC). Here, we aimed to depict the landscape of ASEs, as well as to identify the differential ASEs in steatotic liver graft and their association with tumor recurrence after transplantation. The overall portrait of intragraft transcripts and ASEs were elucidated through RNA sequencing with the liver graft biopsies from patients and rat transplant models. Various differential ASEs were identified in steatotic liver grafts. CYP2E1, ADH1A, CYP2C8, ADH1C, and HGD, as corresponding genes to the common pathways involved differential ASEs in human and rats, were significantly associated with HCC patients' survival. The differential ASEs related RNA-binding proteins (RBPs) were enriched in metabolic pathways. The altered immune cell distribution, particularly macrophages and neutrophils, were perturbated by differential ASEs. The cancer hallmarks were enriched in steatotic liver grafts and closely associated with differential ASEs. Our work identified the differential ASE network with metabolic RBPs, immune cell distribution, and cancer hallmarks in steatotic liver grafts. We verified the link between steatotic liver graft injury and tumor recurrence at post-transcriptional level, offered new evidence to explore metabolism and immune responses, and provided the potential prognostic and therapeutic markers for tumor recurrence.

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