| Literature DB >> 27673353 |
Shu-Xiang Cui1, Xin-Feng Yu2, Xian-Jun Qu2.
Abstract
Des-γ-carboxyprothrombin (DCP), an abnormal prothrombin produced in human hepatocellular carcinoma (HCC), plays crucial roles in the progression of HCC. DCP binding to cellular mesenchymal-epithelial transition factor (c-Met) is an initial event and consequently stimulates HCC through the increase of c-Met-Janus kinase 1- signal transducers and activators of transcription pathways. DCP stimulates HCC invasion through activation of matrix metalloproteinase via upregulation of extracellular signal-regulated kinase-mitogen-activated protein kinase (MAPK) pathway. DCP stimulates HCC angiogenesis through activation of the DCP-kinase insert domain receptor-phospholipaseC-γ-MAPK pathway. Identification of these pathways is important for designing the therapeutic strategy for HCC.Entities:
Keywords: Human hepatocellular carcinoma (HCC); KDR–PLC-γ–MAPK pathway; angiogenesis; angiogenic stimulator; autologous growth factor; c-Met–JAK–STAT3 pathway; des-γ-carboxyprothrombin (DCP)
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Year: 2016 PMID: 27673353 DOI: 10.1080/07357907.2016.1227445
Source DB: PubMed Journal: Cancer Invest ISSN: 0735-7907 Impact factor: 2.176