Lee Nikki P, Wu Haiyang, Ng Kevin T P, Luo Ruibang, Lam Tak-Wah, Lo Chung-Mau, Man Kwan
Department of Surgery, The University of Hong Kong, Hong Kong, China.
Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang University, Hangzhou 310003, China.
Biomedicines. 2018 Apr 6;6(2):41. doi: 10.3390/biomedicines6020041.
Liver transplantation remains the treatment of choice for a selected group of hepatocellular carcinoma (HCC) patients. However, the long-term benefit is greatly hampered by post-transplant HCC recurrence. Our previous studies have identified liver graft injury as an acute phase event leading to post-transplant tumor recurrence.
To re-examine this acute phase event at the molecular level and in an unbiased way, RNA sequencing (RNA-Seq) was performed on liver graft biopsies obtained from the transplant recipients two hours after portal vein reperfusion with an aim to capture frequently altered pathways that account for post-transplant tumor recurrence. Liver grafts from recurrent recipients ( = 6) were sequenced and compared with those from recipients without recurrence ( = 5).
RNA expression profiles comparison pointed to several frequently altered pathways, among which pathways related to cell adhesion molecules were the most involved. Subsequent validation using quantitative polymerase chain reaction confirmed the differential involvement of two cell adhesion molecules (hemochromatosis) and and their related molecules in the acute phase event.
This whole transcriptome strategy unravels the molecular landscape of liver graft gene expression alterations, which can identify key pathways and genes that are involved in acute phase liver graft injury that may lead to post-transplant tumor recurrence.
肝移植仍然是特定肝细胞癌(HCC)患者的首选治疗方法。然而,移植后HCC复发极大地阻碍了其长期疗效。我们之前的研究已确定肝移植损伤是导致移植后肿瘤复发的急性期事件。
为了在分子水平上以无偏倚的方式重新审视这一急性期事件,对门静脉再灌注两小时后从移植受者获取的肝移植活检组织进行RNA测序(RNA-Seq),旨在捕捉导致移植后肿瘤复发的常见改变通路。对复发受者(n = 6)的肝移植组织进行测序,并与未复发受者(n = 5)的肝移植组织进行比较。
RNA表达谱比较指出了几个常见改变的通路,其中与细胞粘附分子相关的通路最为相关。随后使用定量聚合酶链反应进行的验证证实了两种细胞粘附分子(血色素沉着症)和及其相关分子在急性期事件中的差异参与情况。
这种全转录组策略揭示了肝移植基因表达改变的分子格局,可识别参与急性期肝移植损伤的关键通路和基因,这些损伤可能导致移植后肿瘤复发。