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Loss of c-Jun N-terminal Kinase 1 and 2 Function in Liver Epithelial Cells Triggers Biliary Hyperproliferation Resembling Cholangiocarcinoma. | LitMetric

AI Article Synopsis

Article Abstract

Targeted inhibition of the c-Jun N-terminal kinases (JNKs) has shown therapeutic potential in intrahepatic cholangiocarcinoma (CCA)-related tumorigenesis. However, the cell-type-specific role and mechanisms triggered by JNK in liver parenchymal cells during CCA remain largely unknown. Here, we aimed to investigate the relevance of JNK1 and JNK2 function in hepatocytes in two different models of experimental carcinogenesis, the dethylnitrosamine (DEN) model and in nuclear factor kappa B essential modulator (NEMO) mice, focusing on liver damage, cell death, compensatory proliferation, fibrogenesis, and tumor development. Moreover, regulation of essential genes was assessed by reverse transcription polymerase chain reaction, immunoblottings, and immunostainings. Additionally, specific inhibition in hepatocytes of NEMO/JNK1 mice was performed using small interfering (si) RNA (si) nanodelivery. Finally, active signaling pathways were blocked using specific inhibitors. Compound deletion of and in hepatocytes diminished hepatocellular carcinoma (HCC) in both the DEN model and in NEMO mice but in contrast caused massive proliferation of the biliary ducts. Indeed, deficiency in hepatocytes of NEMO (NEMO/JNK) animals caused elevated fibrosis, increased apoptosis, increased compensatory proliferation, and elevated inflammatory cytokines expression but reduced HCC. Furthermore, si treatment in NEMO/JNK1 mice recapitulated the phenotype of NEMO/JNK mice. Next, we sought to investigate the impact of molecular pathways in response to compound JNK deficiency in NEMO mice. We found that NEMO/JNK livers exhibited overexpression of the interleukin-6/signal transducer and activator of transcription 3 pathway in addition to epidermal growth factor receptor (EGFR)-rapidly accelerated fibrosarcoma (Raf)-mitogen-activated protein kinase kinase (MEK)-extracellular signal-regulated kinase (ERK) cascade. The functional relevance was tested by administering lapatinib, which is a dual tyrosine kinase inhibitor of erythroblastic oncogene B-2 (ErbB2) and EGFR signaling, to NEMO/JNK mice. Lapatinib effectively inhibited cystogenesis, improved transaminases, and effectively blocked EGFR-Raf-MEK-ERK signaling. : We define a novel function of JNK1/2 in cholangiocyte hyperproliferation. This opens new therapeutic avenues devised to inhibit pathways of cholangiocarcinogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7262317PMC
http://dx.doi.org/10.1002/hep4.1495DOI Listing

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