Epigenetics of cancer stem cells: Pathways and therapeutics

被引:96
作者
Shukla, Samriddhi [1 ]
Meeran, Syed Musthapa [1 ]
机构
[1] CSIR, Cent Drug Res Inst, Div Endocrinol, Lab Canc Epigenet, Lucknow 226031, Uttar Pradesh, India
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2014年 / 1840卷 / 12期
关键词
Cancer stem cell; Epigenetic reprogramming; DNA methylation; Chromatin remodelling; Chemo-resistance; Chemotherapy; EPITHELIAL-MESENCHYMAL TRANSITION; CHROMATIN REMODELING COMPLEXES; ACUTE MYELOID-LEUKEMIA; BREAST-CANCER; DNA METHYLATION; SELF-RENEWAL; STEM/PROGENITOR CELLS; TUMOR PROGRESSION; SOMATIC-CELLS; PLURIPOTENCY;
D O I
10.1016/j.bbagen.2014.09.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Epigenetic alterations including DNA methylation and histone modifications are the key factors in the differentiation of stem cells into different tissue subtypes. The generation of cancer stem cells (CSCs) in the process of carcinogenesis may also involve similar kind of epigenetic reprogramming where, in contrast, it leads to the loss of expression of genes specific to the differentiated state and regaining of stem cell-specific characteristics. The most important predicament with treatment of cancers includes the non-responsive quiescent CSC. Scope of review: The distinctive capabilities of the CSCs make cancer treatment even more difficult as this population of cells tends to remain quiescent for longer intervals and then gets reactivated leading to tumor relapse. Therefore, the current review is aimed to focus on recent advances in understanding the relation of epigenetic reprogramming to the generation, self-renewal and proliferation of CSCs. Major conclusion: CSC-targeted therapeutic approaches would improve the chances of patient survival by reducing the frequency of tumor relapse. Differentiation therapy is an emerging therapeutic approach in which the CSCs are induced to differentiate from their quiescent state to a mature differentiated form, through activation of differentiation-related signalling pathways, miRNA-mediated alteration and epigenetic differentiation therapy. Thus, understanding the origin of CSC and their epigenetic regulation is crucial to develop treatment strategy against not only for the heterogeneous population of cancer cells but also to CSCs. General significance: Characterizing the epigenetic marks of CSCs and the associated signalling cascades might help in developing therapeutic strategies against chemo-resistant cancers. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:3494 / 3502
页数:9
相关论文
共 117 条
[1]  
Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940
[2]   A gene expression signature shared by human mature oocytes and embryonic stem cells [J].
Assou, Said ;
Cerecedo, Doris ;
Tondeur, Sylvie ;
Pantesco, Veronique ;
Hovatta, Outi ;
Klein, Bernard ;
Hamamah, Samir ;
De Vos, John .
BMC GENOMICS, 2009, 10
[3]   Epigenetic regulation of CD133 and tumorigenicity of CD133+ovarian cancer cells [J].
Baba, T. ;
Convery, P. A. ;
Matsumura, N. ;
Whitaker, R. S. ;
Kondoh, E. ;
Perry, T. ;
Huang, Z. ;
Bentley, R. C. ;
Mori, S. ;
Fujii, S. ;
Marks, J. R. ;
Berchuck, A. ;
Murphy, S. K. .
ONCOGENE, 2009, 28 (02) :209-218
[4]   Epigenetic regulation of ABCG2 gene is associated with susceptibility to xenobiotic exposure [J].
Babu, Kavitha ;
Zhang, Jinbi ;
Moloney, Stephanie ;
Pleasants, Tony ;
McLean, Cameron A. ;
Phua, Sin H. ;
Sheppard, Allan M. .
JOURNAL OF PROTEOMICS, 2012, 75 (12) :3410-3418
[5]   A decade of exploring the cancer epigenome - biological and translational implications [J].
Baylin, Stephen B. ;
Jones, Peter A. .
NATURE REVIEWS CANCER, 2011, 11 (10) :726-734
[6]   Role of the cytosine DNA-methyltransferase and p16INK4a genes in the development of mouse lung tumors [J].
Belinsky, SA .
EXPERIMENTAL LUNG RESEARCH, 1998, 24 (04) :463-479
[7]   A bivalent chromatin structure marks key developmental genes in embryonic stem cells [J].
Bernstein, BE ;
Mikkelsen, TS ;
Xie, XH ;
Kamal, M ;
Huebert, DJ ;
Cuff, J ;
Fry, B ;
Meissner, A ;
Wernig, M ;
Plath, K ;
Jaenisch, R ;
Wagschal, A ;
Feil, R ;
Schreiber, SL ;
Lander, ES .
CELL, 2006, 125 (02) :315-326
[8]   Reprogramming towards pluripotency requires AID-dependent DNA demethylation [J].
Bhutani, Nidhi ;
Brady, Jennifer J. ;
Damian, Mara ;
Sacco, Alessandra ;
Corbel, Stephane Y. ;
Blau, Helen M. .
NATURE, 2010, 463 (7284) :1042-U57
[9]   The roles of transforming growth factor-β, Wnt, Notch and hypoxia on liver progenitor cells in primary liver tumours (Review) [J].
Bogaerts, Eliene ;
Heindryckx, Femke ;
Vandewynckel, Yves-Paul ;
Van Grunsven, Leo A. ;
Van Vlierberghe, Hans .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2014, 44 (04) :1015-1022
[10]   Notch signalling in cancer stem cells [J].
Bolos, Victoria ;
Blanco, Moises ;
Medina, Vanessa ;
Aparicio, Guadalupe ;
Diaz-Prado, Silvia ;
Grande, Enrique .
CLINICAL & TRANSLATIONAL ONCOLOGY, 2009, 11 (01) :11-19