Ffrench Brendan, Gasch Claudia, O'Leary John J, Gallagher Michael F
Department of Histopathology, Trinity College Dublin, Trinity Centre for Health Sciences, St James Hospital, Dublin 8, Ireland.
Mol Cancer. 2014 Dec 11;13:262. doi: 10.1186/1476-4598-13-262.
Despite decades of research, ovarian cancer is still associated with unacceptably high mortality rates, which must be addressed by novel therapeutic approaches. One avenue through which this may be achieved is targeting of tumor-initiating 'Cancer Stem Cells' (CSCs). CSCs are sufficient to generate primary and recurrent disease through extensive rounds of asymmetric division, which maintain the CSC pool while producing the tissues that form the bulk of the tumor. CSCs thrive in the harsh tumor niche, are generally refractory to therapeutic intervention and closely-linked to the Epithelial-Mesenchymal Transition process, which facilitates invasion and metastasis. While it is well-accepted that CSC-targeting must be assessed as a novel therapeutic avenue, few ovarian CSC models have been developed due to perceived and actual difficulties associated with the process of 'CSC Discovery'. In this article we review contemporary approaches to CSC Discovery and argue that this process should start with an understanding of the specific challenges associated with clinical intervention, laying the pipeline backwards towards CSC Discovery. Such an approach would expedite the bridging of the gap between laboratory isolation and clinical targeting of ovarian CSCs.
尽管经过了数十年的研究,卵巢癌的死亡率仍然高得令人难以接受,必须通过新的治疗方法来解决这一问题。实现这一目标的一条途径是靶向肿瘤起始的“癌症干细胞”(CSCs)。癌症干细胞足以通过大量的不对称分裂产生原发性和复发性疾病,这种分裂在维持癌症干细胞库的同时,产生构成肿瘤主体的组织。癌症干细胞在恶劣的肿瘤微环境中茁壮成长,通常对治疗干预具有抗性,并且与上皮-间质转化过程密切相关,该过程促进侵袭和转移。虽然人们普遍认为必须将靶向癌症干细胞作为一种新的治疗途径进行评估,但由于“癌症干细胞发现”过程中存在的实际困难和人们所感知到的困难,很少有卵巢癌癌症干细胞模型被开发出来。在本文中,我们回顾了当代癌症干细胞发现的方法,并认为这个过程应该从了解与临床干预相关的具体挑战开始,朝着癌症干细胞发现逆向构建流程。这样的方法将加快弥合卵巢癌癌症干细胞实验室分离和临床靶向之间的差距。