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  4. Sonic hedgehog pathway inhibitor mitigates mouse hepatocellular carcinoma
 
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Sonic hedgehog pathway inhibitor mitigates mouse hepatocellular carcinoma

Journal
American journal of surgery
Journal Volume
210
Journal Issue
3
Pages
554-560
Date Issued
2015
Author(s)
CHI-JUEI JENG  
DOI
10.1016/j.amjsurg.2015.03.001
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-84945994105&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/391019
Abstract
Background Hepatocellular carcinoma (HCC) is a leading cause of death in Asian countries. Sonic hedgehog (Shh) pathway plays a role in hepatocarcinogenesis. We investigated the treatment effect of mouse HCC with Shh inhibitor GDC-0449. Methods Mouse hepatoma ML-1 cells were implanted in B6 mice. Fifteen days later, GDC-0449 (vismodegib), antagonist of smoothened, was used to treat HCC-bearing mice. The tumor size and liver histopathological features were analyzed, as well as gene expression in Shh pathways. Results GDC-0449 treatment effectively reduced tumor size and cell infiltration of the HCC in mice. Gene expression of Shh pathway molecules was altered, including upregulated Shh expression and downregulated smoothened expression in tumor fractions after GDC-0449 treatment. Conclusion GDC-0449 could effectively mitigate HCC growth in vivo. ? 2015 Elsevier Inc. All rights reserved.
Subjects
GDC-0449; Gli-1; Ptch-1; Shh; Smo; Sonic hedgehog pathway
SDGs

[SDGs]SDG3

Other Subjects
messenger RNA; sonic hedgehog protein; transcription factor Gli1; vismodegib; anilide; antineoplastic agent; cell surface receptor; G protein coupled receptor; GLI1 protein, human; messenger RNA; patched receptors; pyridine derivative; Shh protein, mouse; Smo protein, mouse; sonic hedgehog protein; transcription factor; vismodegib; animal cell; animal experiment; animal model; animal tissue; Article; cancer growth; cancer size; cell infiltration; controlled study; down regulation; drug efficacy; drug megadose; gene expression; histopathology; in vivo study; liver carcinogenesis; liver cell carcinoma; male; mouse; nonhuman; priority journal; protein expression; real time polymerase chain reaction; upregulation; animal; antagonists and inhibitors; C57BL mouse; Carcinoma, Hepatocellular; genetics; Liver Neoplasms, Experimental; metabolism; pathology; randomization; Anilides; Animals; Antineoplastic Agents; Carcinoma, Hepatocellular; Down-Regulation; Gene Expression; Hedgehog Proteins; Liver Neoplasms, Experimental; Male; Mice, Inbred C57BL; Pyridines; Random Allocation; Receptors, Cell Surface; Receptors, G-Protein-Coupled; RNA, Messenger; Transcription Factors; Up-Regulation
Type
journal article

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