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Developing ovarian cancer stem cell models: laying the pipeline from discovery to clinical intervention

机译:建立卵巢癌干细胞模型:铺设从发现到临床干预的管道

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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.
机译:尽管进行了数十年的研究,但卵巢癌仍然伴随着令人无法接受的高死亡率,这必须通过新颖的治疗方法来解决。可以实现这一目标的途径之一是针对肿瘤引发的“癌干细胞”(CSC)。 CSCs通过广泛的不对称分裂过程足以产生原发性和复发性疾病,这种分裂维持了CSC池,同时产生了构成肿瘤大部分的组织。 CSC在恶劣的肿瘤环境中iche壮成长,通常对治疗干预不具抵抗力,并且与上皮-间充质转化过程密切相关,上皮-间质转化过程促进了侵袭和转移。虽然必须将靶向CSC的治疗作为一种新颖的治疗途径进行评估,但是由于与“ CSC发现”过程相关的感知和实际困难,很少开发出卵巢CSC模型。在本文中,我们回顾了当代CSC发现的方法,并认为该过程应从对与临床干预相关的特定挑战的理解开始,从而向CSC Discovery倒退。这种方法将加速缩小实验室隔离与卵巢癌干细胞临床靶向之间的差距。

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