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Differentiation-inducing Therapeutic Effect of Notch Inhibition in Reversing Malignant Transformation of Liver Normal Stem Cells Via MET

Overview
Journal Oncotarget
Specialty Oncology
Date 2018 May 4
PMID 29721169
Citations 7
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Abstract

Background: Liver cancer stem cells (LCSCs) are the key factors for cancer metastasis, recurrent, and drug resistance. LCSCs are originated from either hepatocytes dedifferentiation or differentiation arresting of liver normal stem cells (LNSCs). Differentiation-inducing therapy is a novel strategy in solid tumors. Furthermore, Notch signaling pathway has been proved to play important role in the process of hepatocytes differentiation. In previous study, a malignant transformation cellular model of LNSCs has been built up, and in this study we are trying to illustrate whether inhibition of Notch can reverse this malignant tendency and drive these malignant cells back to differentiate into mature hepatocytes.

Results: Inhibition of Notch signaling pathway can down-regulate the stemness-related cancer markers, lower the proliferative status, alleviate the invasive characteristic, or attenuate the metastasis tendency. What is more, it can help the malignantly transformed cells to regain the mature hepatic function of glucagon synthesis, urea metabolism, albumin production, and indocyanine-green (ICG) clearance.

Materials And Methods: HOX transcript antisense RNA (HOTAIR) expression was enhanced in LNSCs via lentivirus transduction to set up the malignant transformation cellular model. Then, a Notch inhibitor was applied to induce malignantly transformed cells differentiate into mature hepatocytes, and malignant abilities of proliferation, invasiveness, tumorigenesis as well as mature hepatocyte function were observed and compared.

Conclusions: The data demonstrate that the anti-tumor effects of Notch inhibition may lie not only on killing the cancer cells or LCSCs directly, it can also induce the LCSCs differentiation into mature hepatocytes via mesenchymal-epithelial transition (MET) progress or downgrade the malignancy.

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References
1.
Yimlamai D, Christodoulou C, Galli G, Yanger K, Pepe-Mooney B, Gurung B . Hippo pathway activity influences liver cell fate. Cell. 2014; 157(6):1324-1338. PMC: 4136468. DOI: 10.1016/j.cell.2014.03.060. View

2.
Zhang Y, Song W, Zhang F, Liu W, Dou K . Differentiation-inducing activity of hydroxycamptothecin on cancer stem-like cells derived from hepatocellular carcinoma. Dig Dis Sci. 2011; 56(8):2473-81. DOI: 10.1007/s10620-011-1601-6. View

3.
Lu J, Zhou Y, Hu T, Zhang H, Shen M, Cheng P . Notch Signaling Coordinates Progenitor Cell-Mediated Biliary Regeneration Following Partial Hepatectomy. Sci Rep. 2016; 6:22754. PMC: 4782135. DOI: 10.1038/srep22754. View

4.
Wang T, Chen T, Liang H, Yan H, Lin N, Liu L . Notch inhibition promotes fetal liver stem/progenitor cells differentiation into hepatocytes via the inhibition of HNF-1β. Cell Tissue Res. 2014; 357(1):173-84. DOI: 10.1007/s00441-014-1825-9. View

5.
Tofilon P, Vines C, Milas L . Enhancement of in vitro chemotherapeutic activity by dimethylsulfoxide. Clin Exp Metastasis. 1985; 3(2):141-50. DOI: 10.1007/BF01758962. View