Passman Adam M, Low Jasmine, London Roslyn, Tirnitz-Parker Janina E E, Miyajima Atsushi, Tanaka Minoru, Strick-Marchand Helene, Darlington Gretchen J, Finch-Edmondson Megan, Ochsner Scott, Zhu Cornelia, Whelan James, Callus Bernard A, Yeoh George C T
School of Chemistry and Biochemistry, The University of Western Australia, Crawley, WA 6009, Australia; The Centre for Medical Research, Harry Perkins Institute of Medical Research, Nedlands, WA 6009, Australia.
School of Chemistry and Biochemistry, The University of Western Australia, Crawley, WA 6009, Australia; ARC Centre of Excellence in Plant Energy Biology, The University of Western Australia, Crawley, WA 6009, Australia.
Stem Cells Int. 2016;2016:5702873. doi: 10.1155/2016/5702873. Epub 2016 Oct 3.
Liver progenitor cells (LPCs) can proliferate extensively, are able to differentiate into hepatocytes and cholangiocytes, and contribute to liver regeneration. The presence of LPCs, however, often accompanies liver disease and hepatocellular carcinoma (HCC), indicating that they may be a cancer stem cell. Understanding LPC biology and establishing a sensitive, rapid, and reliable method to detect their presence in the liver will assist diagnosis and facilitate monitoring of treatment outcomes in patients with liver pathologies. A transcriptomic meta-analysis of over 400 microarrays was undertaken to compare LPC lines against datasets of muscle and embryonic stem cell lines, embryonic and developed liver (DL), and HCC. Three gene clusters distinguishing LPCs from other liver cell types were identified. Pathways overrepresented in these clusters denote the proliferative nature of LPCs and their association with HCC. Our analysis also revealed 26 novel markers, LPC markers, including and , and eight known LPC markers, including and . These markers specified the presence of LPCs in pathological liver tissue by qPCR and correlated with LPC abundance determined using immunohistochemistry. These results showcase the value of global transcript profiling to identify pathways and markers that may be used to detect LPCs in injured or diseased liver.
肝祖细胞(LPCs)能够广泛增殖,可分化为肝细胞和胆管细胞,并参与肝脏再生。然而,LPCs的存在常与肝脏疾病和肝细胞癌(HCC)相伴,这表明它们可能是癌症干细胞。了解LPC生物学特性并建立一种灵敏、快速且可靠的方法来检测其在肝脏中的存在,将有助于肝脏疾病患者的诊断并便于监测治疗效果。我们对400多个微阵列进行了转录组元分析,以将LPC系与肌肉和胚胎干细胞系、胚胎及发育肝脏(DL)以及HCC的数据集进行比较。确定了三个区分LPCs与其他肝细胞类型的基因簇。这些簇中过度表达的通路表明了LPCs的增殖特性及其与HCC的关联。我们的分析还揭示了26个新的标记物,即LPC标记物,包括 和 ,以及8个已知的LPC标记物,包括 和 。这些标记物通过定量PCR确定了病理肝脏组织中LPCs的存在,并与使用免疫组织化学测定的LPC丰度相关。这些结果展示了全局转录谱分析在识别可用于检测受损或患病肝脏中LPCs的通路和标记物方面的价值。