Targeting liver cancer stem cells for the treatment of hepatocellular carcinoma

被引:31
作者
Li, Na [2 ]
Zhu, Ying [1 ]
机构
[1] Dalian Med Univ, Affiliated Hosp 1, Dept Infect Dis, Dalian 116011, Liaoning, Peoples R China
[2] Dalian Med Univ, Affiliated Hosp 1, Dalian, Peoples R China
基金
中国国家自然科学基金;
关键词
drug resistance; HCC treatment; hepatocellular carcinoma; liver cancer stem cells; targeting LCSCs; PROMOTES SELF-RENEWAL; EPITHELIAL-MESENCHYMAL TRANSITION; POTENTIAL THERAPEUTIC TARGET; TUMOR-INITIATING CELLS; DRUG-RESISTANCE; DOWN-REGULATION; MALIGNANT-TRANSFORMATION; SYNERGISTIC INHIBITION; TRANSCRIPTION FACTOR; SIGNALING PATHWAY;
D O I
10.1177/1756284818821560
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Liver cancer is one of the most common malignant tumors and prognosis remains poor. It has been increasingly recognized that liver cancer stem cells (LCSCs) are responsible for the carcinogenesis, recurrence, metastasis and chemoresistance of hepatocellular carcinoma (HCC). Targeting LCSCs is promising to be a new direction for the treatment of HCC. Herein, we summarize the potentially therapeutic targets in LCSCs at the level of genes, molecules and cells, such as knockout of oncogenes or oncoproteins, restoring the silent tumor suppressor genes, inhibition of the transcription factors and regulation of noncoding RNAs (including microRNAs and long noncoding RNAs) in LCSCs at the genetic level; inhibition of markers and blockade of the key signaling pathways of LCSCs at the molecular level; and inhibiting autophagy and application of oncolytic adenoviruses in LCSCs at the cellular level. Moreover, we analyze the potential targets in LCSCs to eliminate chemoresistance of HCC. Thereinto, the suppression of autophagy and Nanog by chloroquine and shRNA respectively may be the most promising targeting approaches. These targets may provide novel therapeutic strategies for the treatment of HCC by targeting LCSCs.
引用
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页数:22
相关论文
共 158 条
[1]   Oncolytic Adenoviruses in Cancer Treatment [J].
Alemany, Ramon .
BIOMEDICINES, 2014, 2 (01) :36-49
[2]   Inflammatory related gene IKKα, IKKβ, IKKγ cooperates to determine liver cancer stem cells progression by altering telomere via heterochromatin protein 1-HOTAIR axis [J].
An, Jiahui ;
Wu, Mengying ;
Xin, Xiaoru ;
Lin, Zhuojia ;
Li, Xiaonan ;
Zheng, Qidi ;
Gui, Xin ;
Li, Tianming ;
Pu, Hu ;
Li, Haiyan ;
Lu, Dongdong .
ONCOTARGET, 2016, 7 (31) :50131-50149
[3]   TWISTing an embryonic transcription factor into an oncoprotein [J].
Ansieau, S. ;
Morel, A-P ;
Hinkal, G. ;
Bastid, J. ;
Puisieux, A. .
ONCOGENE, 2010, 29 (22) :3173-3184
[4]   Ptpn11/Shp2 Acts as a Tumor Suppressor in Hepatocellular Carcinogenesis [J].
Bard-Chapeau, Emilie A. ;
Li, Shuangwei ;
Ding, Jin ;
Zhang, Sharon S. ;
Zhu, Helen H. ;
Princen, Frederic ;
Fang, Diane D. ;
Han, Tao ;
Bailly-Maitre, Beatrice ;
Poli, Valeria ;
Varki, Nissi M. ;
Wang, Hongyang ;
Feng, Gen-Sheng .
CANCER CELL, 2011, 19 (05) :629-639
[5]  
Barh D, 2010, CURR ONCOL, V17, P70
[6]   Numb prevents a complete epithelial-mesenchymal transition by modulating Notch signalling [J].
Bocci, Federico ;
Jolly, Mohit K. ;
Tripathi, Satyendra C. ;
Aguilar, Mitzi ;
Hanash, Samir M. ;
Levine, Herbert ;
Onuchic, Jose N. .
JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2017, 14 (136)
[7]   The emerging role of p53 in stem cells [J].
Bonizzi, Giuseppina ;
Cicalese, Angelo ;
Insinga, Alessandra ;
Pelicci, Pier Giuseppe .
TRENDS IN MOLECULAR MEDICINE, 2012, 18 (01) :6-12
[8]  
Caiazza Carmen, 2016, Microrna, V5, P113
[9]   The phosphoinositide 3-kinase pathway [J].
Cantley, LC .
SCIENCE, 2002, 296 (5573) :1655-1657
[10]   Octamer 4/MicroRNA-1246 Signaling Axis Drives Wnt/β-Catenin Activation in Liver Cancer Stem Cells [J].
Chai, Stella ;
Ng, Kai-Yu ;
Tong, Man ;
Lau, Eunice Y. ;
Lee, Terence K. ;
Chan, Kwok Wah ;
Yuan, Yun-Fei ;
Cheung, Tan-To ;
Cheung, Siu-Tim ;
Wang, Xiao-Qi ;
Wong, Nathalie ;
Lo, Chung-Mau ;
Man, Kwan ;
Guan, Xin-Yuan ;
Ma, Stephanie .
HEPATOLOGY, 2016, 64 (06) :2062-2076