Current Status of Gene Therapy in Hepatocellular Carcinoma

被引:55
作者
Reghupaty, Saranya Chidambaranathan [1 ]
Sarkar, Devanand [1 ]
机构
[1] Virginia Commonwealth Univ, Inst Mol Med VIMM, Massey Canc Ctr, Dept Human & Mol Genet, Richmond, VA 23298 USA
关键词
HCC; gene therapy; clinical trials; nanoparticles; viruses; EPITHELIAL-MESENCHYMAL TRANSITION; MESOPOROUS SILICA NANOPARTICLES; TUMOR-SUPPRESSOR; LIPID NANOPARTICLES; CELL-PROLIFERATION; DOWN-REGULATION; GROWTH-FACTOR; CO-DELIVERY; METASTASIS; EXPRESSION;
D O I
10.3390/cancers11091265
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is the fifth most common cancer and the second leading cause of cancer related deaths world-wide. Liver transplantation, surgical resection, trans-arterial chemoembolization, and radio frequency ablation are effective strategies to treat early stage HCC. Unfortunately, HCC is usually diagnosed at an advanced stage and there are not many treatment options for late stage HCC. First-line therapy for late stage HCC includes sorafenib and lenvatinib. However, these treatments provide only an approximate three month increase in survival. Besides, they cannot specifically target cancer cells that lead to a wide array of side effects. Patients on these drugs develop resistance within a few months and have to rely on second-line therapy that includes regorafenib, pembrolizumab, nivolumab, and cabometyx. These disadvantages make gene therapy approach to treat HCC an attractive option. The two important questions that researchers have been trying to answer in the last 2-3 decades are what genes should be targeted and what delivery systems should be used. The objective of this review is to analyze the changing landscape of HCC gene therapy, with a focus on these two questions.
引用
收藏
页数:21
相关论文
共 108 条
[1]  
[Anonymous], 2018, Med Lett Drugs Ther, V60, pe122
[2]  
[Anonymous], 2017, MED LETT DRUGS THER, V59, P177
[3]   Indoleamine 2,3-dioxygenase: As a potential prognostic marker and immunotherapeutic target for hepatocellular carcinoma [J].
Asghar, Kashif ;
Farooq, Asim ;
Zulfiqar, Bilal ;
Rashid, Muhammad Usman .
WORLD JOURNAL OF GASTROENTEROLOGY, 2017, 23 (13) :2286-2293
[4]   Cell-Specific Delivery of Diverse Cargos by Bacteriophage MS2 Virus-like Particles [J].
Ashley, Carlee E. ;
Carnes, Eric C. ;
Phillips, Genevieve K. ;
Durfee, Paul N. ;
Buley, Mekensey D. ;
Lino, Christopher A. ;
Padilla, David P. ;
Phillips, Brandy ;
Carter, Mark B. ;
Willman, Cheryl L. ;
Brinker, C. Jeffrey ;
Caldeira, Jerri do Carmo ;
Chackerian, Bryce ;
Wharton, Walker ;
Peabody, David S. .
ACS NANO, 2011, 5 (07) :5729-5745
[5]   Lentivirus-mediated RNAi knockdown of insulin- like growth factor-1 receptor inhibits the growth and invasion of hepatocellular carcinoma via down-regulating midkine expression [J].
Bie, Cai Qun ;
Liu, Xu You ;
Cao, Ming Rong ;
Huang, Qiu Yan ;
Tang, Hui Jun ;
Wang, Min ;
Cao, Guo Li ;
Yi, Ting Zhuang ;
Wu, Sheng Lan ;
Xu, Wei Jie ;
Tang, Shao Hui .
ONCOTARGET, 2016, 7 (48) :79291-79304
[6]   Nanoparticle-formulated siRNA targeting integrins inhibits hepatocellular carcinoma progression in mice [J].
Bogorad, Roman L. ;
Yin, Hao ;
Zeigerer, Anja ;
Nonaka, Hidenori ;
Ruda, Vera M. ;
Zerial, Marino ;
Anderson, Daniel G. ;
Koteliansky, Victor .
NATURE COMMUNICATIONS, 2014, 5
[7]   Recent developments of c-Met as a therapeutic target in hepatocellular carcinoma [J].
Bouattour, Mohamed ;
Raymond, Eric ;
Qin, Shukui ;
Cheng, Ann-Lii ;
Stammberger, Uz ;
Locatelli, Giuseppe ;
Faivre, Sandrine .
HEPATOLOGY, 2018, 67 (03) :1132-1149
[8]   The emerging therapeutic potential of the oncolytic immunotherapeutic Pexa-Vec (JX-594) [J].
Breitbach, Caroline J. ;
Bell, John C. ;
Hwang, Tae-Ho ;
Kirn, David H. ;
Burke, James .
ONCOLYTIC VIROTHERAPY, 2015, 4 :25-31
[9]  
Breitbach CJ, 2015, METHODS MOL BIOL, V1317, P341, DOI 10.1007/978-1-4939-2727-2_19
[10]   Glypican-3: A novel serum and histochemical marker for hepatocellular carcinoma [J].
Capurro, M ;
Wanless, IR ;
Sherman, M ;
Deboer, G ;
Shi, W ;
Miyoshi, E ;
Filmus, J .
GASTROENTEROLOGY, 2003, 125 (01) :89-97