Combination treatment with sorafenib and wh-4 additively suppresses the proliferation of liver cancer cells

被引:3
作者
Chen, Su-Hong [1 ,2 ]
Xu, Dan-Dan [2 ]
Zhou, Peng-Jun [1 ]
Wang, Yao [1 ]
Liu, Qiu-Ying [1 ]
Ren, Zhe [1 ]
Liu, Zhong [1 ]
Wang, Xia [2 ]
Huang, Hui-Qing [2 ]
Xue, Xue [2 ]
Wang, Ying [3 ]
Wang, Yi-Fei [1 ]
机构
[1] Jinan Univ, Coll Life Sci & Technol, 601 West Huangpu Rd, Guangzhou 510632, Guangdong, Peoples R China
[2] Guangdong Food & Drug Vocat Coll, Coll Biotechnol, Guangzhou 510520, Guangdong, Peoples R China
[3] Zhongkai Univ Agr & Engn, Coll Food Sci & Technol, 501 Zhongkai Rd, Guangzhou 510225, Guangdong, Peoples R China
关键词
sorafenib; wh-4; combination treatment; proliferation; hepatocellular carcinoma cells; HUMAN HEPATOCELLULAR-CARCINOMA; HEAT-SHOCK PROTEINS; HSP90; INHIBITOR; MULTIDRUG-RESISTANCE; GROWTH; SNX-2112; APOPTOSIS; PATHWAY; EXPRESSION; JAK/STAT;
D O I
10.3892/etm.2022.11156
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Sorafenib is currently used to treat hepatocellular carcinoma (HCC). However, the development of chemoresistance to sorafenib is a major limitation for sorafenib-based therapy in patients with HCC. In the present study, the effect of the combination therapy of sorafenib and wh-4 on the proliferation of liver cancer cells was investigated. The results showed that sorafenib with wh-4 additively suppressed the proliferation of liver cancer cells. The colony formation of liver cancer cells decreased significantly in response to the combination treatment of sorafenib with wh-4, and it also induced the apoptosis of liver cancer cells. Western blot analysis demonstrated decreased expression of Bcl2, and increased expression of Bax in liver cancer cells treated with a combination of sorafenib and wh-4. Moreover, the migration of liver cancer cells was inhibited. The combination treatment of sorafenib with wh-4 reduced the expression levels of ABCB1 and ABCG2 which are responsible for resistance. Finally, STAT3 overexpression abolished the proliferation inhibition effect of sorafenib with wh-4 on liver cancer cells, and sorafenib and wh-4 suppressed the proliferation of liver cancer cells by STAT3 pathway. Together, these results suggest that sorafenib-wh4 combination treatment is a potential novel therapeutic approach to suppress the proliferation of liver cancer cells.
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页数:10
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共 64 条
[1]  
[Anonymous], 2018, Oncotarget, DOI DOI 10.18632/ONCOTARGET.23843
[2]   Antitumor Activity of SNX-2112, a Synthetic Heat Shock Protein-90 Inhibitor, in MET-Amplified Tumor Cells with or without Resistance to Selective MET Inhibition [J].
Bachleitner-Hofmann, Thomas ;
Sun, Mark Y. ;
Chen, Chin-Tung ;
Liska, David ;
Zeng, Zhaoshi ;
Viale, Agnes ;
Olshen, Adam B. ;
Mittlboeck, Martina ;
Christensen, James G. ;
Rosen, Neal ;
Solit, David B. ;
Weiser, Martin R. .
CLINICAL CANCER RESEARCH, 2011, 17 (01) :122-133
[3]   Discovery of benzamide tetrahydro-4H-carbazol-4-ones as novel small molecule inhibitors of Hsp90 [J].
Barta, Thomas E. ;
Veal, James M. ;
Rice, John W. ;
Partridge, Jeffrey M. ;
Fadden, R. Patrick ;
Ma, Wei ;
Jenks, Matthew ;
Geng, Lifeng ;
Hanson, Gunnar J. ;
Huang, Kenneth H. ;
Barabasz, Amy F. ;
Foley, Briana E. ;
Otto, James ;
Hall, Steven E. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (12) :3517-3521
[4]   Multi-kinase inhibitors can associate with heat shock proteins through their NH2-termini by which they suppress chaperone function [J].
Booth, Laurence ;
Shuch, Brian ;
Albers, Thomas ;
Roberts, Jane L. ;
Tavallai, Mehrad ;
Proniuk, Stefan ;
Zukiwski, Alexander ;
Wang, Dasheng ;
Chen, Ching-Shih ;
Bottaro, Don ;
Ecroyd, Heath ;
Lebedyeva, Iryna O. ;
Dent, Paul .
ONCOTARGET, 2016, 7 (11) :12975-12996
[5]   HSP82 IS AN ESSENTIAL PROTEIN THAT IS REQUIRED IN HIGHER CONCENTRATIONS FOR GROWTH OF CELLS AT HIGHER TEMPERATURES [J].
BORKOVICH, KA ;
FARRELLY, FW ;
FINKELSTEIN, DB ;
TAULIEN, J ;
LINDQUIST, S .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (09) :3919-3930
[6]   Efficacy and safety of sorafenib in patients with advanced hepatocellular carcinoma according to baseline status: Subset analyses of the phase III Sorafenib Asia-Pacific trial [J].
Cheng, Ann-Lii ;
Guan, Zhongzhen ;
Chen, Zhendong ;
Tsao, Chao-Jung ;
Qin, Shukui ;
Kim, Jun Suk ;
Yang, Tsai-Sheng ;
Tak, Won Young ;
Pan, Hongming ;
Yu, Shiying ;
Xu, Jianming ;
Fang, Fang ;
Zou, Jessie ;
Lentini, Giuseppe ;
Voliotis, Dimitris ;
Kang, Yoon-Koo .
EUROPEAN JOURNAL OF CANCER, 2012, 48 (10) :1452-1465
[7]   Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial [J].
Cheng, Ann-Lii ;
Kang, Yoon-Koo ;
Chen, Zhendong ;
Tsao, Chao-Jung ;
Qin, Shukui ;
Kim, Jun Suk ;
Luo, Rongcheng ;
Feng, Jifeng ;
Ye, Shenglong ;
Yang, Tsai-Sheng ;
Xu, Jianming ;
Sun, Yan ;
Liang, Houjie ;
Liu, Jiwei ;
Wang, Jiejun ;
Tak, Won Young ;
Pan, Hongming ;
Burock, Karin ;
Zou, Jessie ;
Voliotis, Dimitris ;
Guan, Zhongzhen .
LANCET ONCOLOGY, 2009, 10 (01) :25-34
[8]   Role of the novel HSP90 inhibitor AUY922 in hepatocellular carcinoma: Potential for therapy [J].
Cheng, Wei ;
Ainiwaer, Aimudula ;
Xiao, Lei ;
Cao, Qian ;
Wu, Ge ;
Yang, Ying ;
Mao, Rui ;
Bao, Yongxing .
MOLECULAR MEDICINE REPORTS, 2015, 12 (02) :2451-2456
[9]   A randomized phase II study of paclitaxel alone versus paclitaxel plus sorafenib in second- and third-line treatment of patients with HER2-negative metastatic breast cancer (PASO) [J].
Decker, Thomas ;
Overkamp, Friedrich ;
Roesel, Siegfried ;
Nusch, Arnd ;
Goehler, Thomas ;
Indorf, Martin ;
Sahlmann, Joerg ;
Trarbach, Tanja .
BMC CANCER, 2017, 17
[10]   A prospective clinical trial on sorafenib treatment of hepatocellular carcinoma before liver transplantation [J].
Eilard, Malin Sternby ;
Andersson, Mats ;
Naredi, Peter ;
Geronymakis, Charalampos ;
Lindner, Per ;
Cahlin, Christian ;
Bennet, William ;
Rizell, Magnus .
BMC CANCER, 2019, 19 (1)