Shukla Samriddhi, Meeran Syed Musthapa
Laboratory of Cancer Epigenetics, Division of Endocrinology, CSIR-Central Drug Research Institute, Lucknow, India.
Laboratory of Cancer Epigenetics, Division of Endocrinology, CSIR-Central Drug Research Institute, Lucknow, India.
Biochim Biophys Acta. 2014 Dec;1840(12):3494-3502. doi: 10.1016/j.bbagen.2014.09.017. Epub 2014 Sep 18.
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.
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.
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.
Characterizing the epigenetic marks of CSCs and the associated signalling cascades might help in developing therapeutic strategies against chemo-resistant cancers.
包括DNA甲基化和组蛋白修饰在内的表观遗传改变是干细胞分化为不同组织亚型的关键因素。在致癌过程中癌症干细胞(CSCs)的产生可能也涉及类似的表观遗传重编程,然而,这会导致分化状态特异性基因表达的丧失以及干细胞特异性特征的重新获得。癌症治疗面临的最重要困境包括对治疗无反应的静止CSC。
CSCs的独特能力使癌症治疗更加困难,因为这群细胞往往会长时间保持静止,然后重新激活导致肿瘤复发。因此,本综述旨在聚焦于理解表观遗传重编程与CSCs的产生、自我更新和增殖之间关系的最新进展。
以CSCs为靶点的治疗方法将通过降低肿瘤复发频率来提高患者存活几率。分化疗法是一种新兴的治疗方法,其中通过激活分化相关信号通路、miRNA介导的改变和表观遗传分化疗法,诱导CSCs从静止状态分化为成熟的分化形式。因此,了解CSCs的起源及其表观遗传调控对于制定针对异质性癌细胞群体以及CSCs的治疗策略至关重要。
表征CSCs的表观遗传标记和相关信号级联可能有助于开发针对化疗耐药癌症的治疗策略。