Effects of low concentrations of Regorafenib and Sorafenib on human HCC cell AFP, migration, invasion, and growth in vitro

被引:49
作者
Carr, Brian I. [1 ]
D'Alessandro, Rosalba [1 ]
Refolo, Maria G. [1 ]
Iacovazzi, Palma A. [2 ]
Lippolis, Catia [1 ]
Messa, Caterina [1 ]
Cavallini, Aldo [1 ]
Correale, Mario [2 ]
Di Carlo, Antonio [2 ]
机构
[1] IRCCS S de Bellis, Natl Inst Digest Dis, Biochem Lab, I-70013 Castellana Grotte, BA, Italy
[2] IRCCS S de Bellis, Natl Inst Digest Dis, Clin Pathol Lab, I-70013 Castellana Grotte, BA, Italy
关键词
ALPHA-FETOPROTEIN RESPONSE; RAF/MEK/ERK PATHWAY; TOXICITIES; INHIBITOR; SURVIVAL; TARGETS;
D O I
10.1002/jcp.24291
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Sorafenib was shown in clinical trial to enhance survival in hepatocellular carcinoma (HCC) patients, but with minimal tumor shrinkage. To correlate several indices of HCC growth at various drug concentrations, HCC cells were grown in various low concentrations of two multikinase inhibitors, Regorafenib (Stivarga) and Sorafenib (Nexavar) and their effects were examined on alpha-fetoprotein (AFP), cell growth, migration, and invasion. In two AFP positive human HCC cell lines, AFP was inhibited at 0.11 mu M drug concentrations. Cell migration and invasion were also inhibited at similar low drug concentrations. However, 10-fold higher drug concentrations were required to inhibit cell growth in both AFP positive and negative cells. To investigate this concentration discrepancy of effects, cells were then grown for prolonged times and sub-cultured in low drug concentrations and then their growth was re-tested. The growth in these drug-exposed cells was found to be slower than cells without prior drug exposure and they were also more sensitive to subsequent drug challenge. Evidence was also found for changes in cell signaling pathways in these slow-growth cells. Low multikinase inhibitor concentrations thus modulate several aspects of HCC cell biology. J. Cell. Physiol. 228: 13441350, 2013. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:1344 / 1350
页数:7
相关论文
共 17 条
[1]   Sorafenib (BAY 43-9006, Nexavar®), a dual-action inhibitor that targets RAF/MEK/ERK pathway in tumor cells and tyrosine kinases VEGFR/PDGFR in tumor vasculature [J].
Adnane, Lila ;
Trail, Pamela A. ;
Taylor, Ian ;
Wilhelm, Scott M. .
REGULATORS AND EFFECTORS OF SMALL GTPASES: RAS FAMILY, 2006, 407 :597-+
[2]   Fluoro-Sorafenib (Regorafenib) effects on hepatoma cells: Growth inhibition, quiescence, and recovery [J].
Carr, Brian I. ;
Cavallini, Aldo ;
Lippolis, Catia ;
D'Alessandro, Rosalba ;
Messa, Caterina ;
Refolo, Maria G. ;
Tafaro, Angela .
JOURNAL OF CELLULAR PHYSIOLOGY, 2013, 228 (02) :292-297
[3]   Tumor and liver determinants of prognosis in unresectable hepatocellular carcinoma: a large case cohort study [J].
Carr, Brian I. ;
Pancoska, Petr ;
Branch, Robert A. .
HEPATOLOGY INTERNATIONAL, 2010, 4 (01) :396-405
[4]   Severe clinical toxicities are correlated with survival in patients with advanced renal cell carcinoma treated with sunitinib and sorafenib [J].
Di Fiore, F. ;
Rigal, O. ;
Menager, C. ;
Michel, P. ;
Pfister, C. .
BRITISH JOURNAL OF CANCER, 2011, 105 (12) :1811-1813
[5]   Field-Practice Study of Sorafenib Therapy for Hepatocellular Carcinoma: A Prospective Multicenter Study in Italy [J].
Iavarone, Massimo ;
Cabibbo, Giuseppe ;
Piscaglia, Fabio ;
Zavaglia, Claudio ;
Grieco, Antonio ;
Villa, Erica ;
Camma, Calogero ;
Colombo, Massimo ;
Sangiovanni, Angelo ;
Vavassori, Sara ;
Romeo, Raffaella ;
Di Marco, Vito ;
Craxi, Antonio ;
Borghi, Alberto ;
Granito, Alessandro ;
Bolondi, Luigi ;
Airoldi, Aldo ;
Pinzello, Giovambattista ;
Biolato, Marco ;
Racco, Simona ;
Pompili, Maurizio ;
Lei, Barbara ;
De Maria, Nicola .
HEPATOLOGY, 2011, 54 (06) :2055-2063
[6]   Sorafenib Dose Escalation in the Treatment of Advanced Hepatocellular Carcinoma [J].
Kim, Jeong Eun ;
Ryoo, Baek-Yeol ;
Ryu, Min-Hee ;
Chang, Heung-Moon ;
Suh, Dong Jin ;
Lee, Han Chu ;
Lim, Young-Suk ;
Kim, Kang Mo ;
Kang, Yoon-Koo .
ONCOLOGY, 2012, 82 (02) :119-125
[7]   In vitro scratch assay:: a convenient and inexpensive method for analysis of cell migration in vitro [J].
Liang, Chun-Chi ;
Park, Ann Y. ;
Guan, Jun-Lin .
NATURE PROTOCOLS, 2007, 2 (02) :329-333
[8]   Sorafenib blocks the RAF/MEK/ERK pathway, inhibits tumor angiogenesis, and induces tumor cell apoptosis in hepatocellular carcinoma model PLC/PRF/5 [J].
Liu, Li ;
Cao, Yichen ;
Chen, Charles ;
Zhang, Xiaomei ;
McNabola, Angela ;
Wilkie, Dean ;
Wilhelm, Scott ;
Lynch, Mark ;
Carter, Christopher .
CANCER RESEARCH, 2006, 66 (24) :11851-11858
[9]   Sorafenib in advanced hepatocellular carcinoma [J].
Llovet, Josep M. ;
Ricci, Sergio ;
Mazzaferro, Vincenzo ;
Hilgard, Philip ;
Gane, Edward ;
Blanc, Jean-Frederic ;
Cosme de Oliveira, Andre ;
Santoro, Armando ;
Raoul, Jean-Luc ;
Forner, Alejandro ;
Schwartz, Myron ;
Porta, Camillo ;
Zeuzem, Stefan ;
Bolondi, Luigi ;
Greten, Tim F. ;
Galle, Peter R. ;
Seitz, Jean-Francois ;
Borbath, Ivan ;
Haussinger, Dieter ;
Giannaris, Tom ;
Shan, Minghua ;
Moscovici, Marius ;
Voliotis, Dimitris ;
Bruix, Jordi .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 359 (04) :378-390
[10]   Alpha-fetoprotein response correlates with EASL response and survival in solitary hepatocellular carcinoma treated with transarterial therapies: A subgroup analysis [J].
Memon, Khairuddin ;
Kulik, Laura ;
Lewandowski, Robert J. ;
Wang, Edward ;
Ryu, Robert K. ;
Riaz, Ahsun ;
Nikolaidis, Paul ;
Miller, Frank H. ;
Yaghmai, Vahid ;
Baker, Talia ;
Abecassis, Michael ;
Benson, Al B., III ;
Mulcahy, Mary F. ;
Omary, Reed A. ;
Salem, Riad .
JOURNAL OF HEPATOLOGY, 2012, 56 (05) :1112-1120