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Sorafenib with ASC-J9 ® synergistically suppresses the HCC progression via altering the pSTAT3-CCL2/Bcl2 signals.

Authors :
Xu J
Lin H
Li G
Sun Y
Shi L
Ma WL
Chen J
Cai X
Chang C
Source :
International journal of cancer [Int J Cancer] 2017 Feb 01; Vol. 140 (3), pp. 705-717. Date of Electronic Publication: 2016 Nov 09.
Publication Year :
2017

Abstract

Sorafenib is currently used as a standard treatment to suppress the progression of hepatocellular carcinoma (HCC), especially in advanced stages. However, patients who receive Sorafenib treatment eventually develop resistance without clear mechanisms. There is a great need for better efficacy of Sorafenib treatment in combination with other therapies. Here, we demonstrated that the treatment combining Sorafenib with ASC-J9 <superscript>®</superscript> could synergistically suppress HCC progression via altering cell-cycle regulation, apoptosis and invasion. Mechanism dissection suggests that while Sorafenib impacts little or even slightly increases the activated/phosphorylated STAT3 (p-STAT3), a key stimulator to promote the HCC progression, adding ASC-J9 <superscript>®</superscript> significantly suppresses the p-STAT3 expression and its downstream genes including CCL2 and Bcl2. Interrupting these signals via constitutively active STAT3 partially reverses the synergistic suppression of Sorafenib-ASC-J9 <superscript>®</superscript> combination on HCC progression. In vivo studies further confirmed the synergistic effect of Sorafenib-ASC-J9 <superscript>®</superscript> combination. Together, these results suggest the newly developed Sorafenib-ASC-J9 <superscript>®</superscript> combination is a novel therapy to better suppress HCC progression.<br /> (© 2016 The Authors International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.)

Details

Language :
English
ISSN :
1097-0215
Volume :
140
Issue :
3
Database :
MEDLINE
Journal :
International journal of cancer
Publication Type :
Academic Journal
Accession number :
27668844
Full Text :
https://doi.org/10.1002/ijc.30446