Huang Kuang-Tzu, Kuo I-Ying, Tsai Ming-Chao, Wu Chun-Hsien, Hsu Li-Wen, Chen Li-Yu, Kung Chao-Pin, Cheng Yu-Fan, Goto Shigeru, Chou Yu-Wei, Chen Chao-Long, Lin Chih-Che, Chen Kuang-Den
Institute for Translational Research in Biomedicine, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan; Liver Transplantation Center, Department of Surgery, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan.
Liver Transplantation Center, Department of Surgery, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, Taiwan.
Mol Ther Nucleic Acids. 2017 Dec 15;9:274-283. doi: 10.1016/j.omtn.2017.10.002. Epub 2017 Oct 7.
Hepatocellular carcinoma (HCC) is one of the most common and aggressive malignancies worldwide. Treatment outcomes remain poor mainly due to lack of good diagnostic/prognostic markers and limited therapeutic strategies. We previously characterized aberrant activation of the TF/FVII/PAR2 pathway, which subsequently results in decreased autophagy, as a crucial event in malignant progression of HCC. Here, we identified miR-135a as a highly upregulated miRNA in HCC in response to TF/FVII/PAR2 activation. Analyzing 103 HCC patient specimens, we confirmed that miR-135a was frequently elevated in HCC tissues with higher FVII expression compared to adjacent non-cancerous counterparts. Increased miR-135a levels in HCC were also associated with tumor staging, recurrence, microvascular invasion, and decreased disease-free survival. We subsequently identified Atg14, a key component that regulates the formation of autophagosome as a direct target of miR-135a. Ectopic expression of miR-135a suppressed Atg14 levels and inhibited the autophagic processes. Our results indicate strong positive correlations between miR-135a levels and malignant behaviors in HCC patients and also suggest novel functions of miR-135a in regulation of autophagy, which could be useful as a potential target for prognostic and therapeutic uses.
肝细胞癌(HCC)是全球最常见且侵袭性最强的恶性肿瘤之一。主要由于缺乏良好的诊断/预后标志物以及治疗策略有限,治疗效果仍然较差。我们之前将TF/FVII/PAR2通路的异常激活(随后导致自噬减少)描述为HCC恶性进展中的关键事件。在此,我们鉴定出miR-135a是HCC中因TF/FVII/PAR2激活而高度上调的一种微小RNA。通过分析103例HCC患者标本,我们证实与相邻非癌组织相比,miR-135a在FVII表达较高的HCC组织中经常升高。HCC中miR-135a水平升高还与肿瘤分期、复发、微血管侵犯以及无病生存期缩短相关。我们随后鉴定出Atg14(一种调节自噬体形成的关键成分)是miR-135a的直接靶标。miR-135a的异位表达抑制了Atg14水平并抑制了自噬过程。我们的结果表明miR-135a水平与HCC患者的恶性行为之间存在强正相关,并且还提示了miR-135a在自噬调节中的新功能,这可能作为预后和治疗用途的潜在靶点。