Cancer stem cell (a)symmetry & plasticity: Tumorigenesis and therapy

被引:70
|
作者
Najafi, Masoud [1 ]
Mortezaee, Keywan [2 ]
Ahadi, Reza [3 ]
机构
[1] Kermanshah Univ Med Sci, Sch Paramed Sci, Radiol & Nucl Med Dept, Kermanshah, Iran
[2] Kurdistan Univ Med Sci, Sch Med, Dept Anat, Sanandaj, Iran
[3] Iran Univ Med Sci, Sch Med, Dept Anat, Tehran, Iran
关键词
Cancer stem cell (CSC); Niche; Plasticity; Asymmetric division (AD); Symmetric division (SD); Dedifferentiation; Tumor microenvironment (TME); Resistance; Stemness; Quiescence; Epithelial-mesenchymal transition (EMT); Numb; TUMOR-INITIATING CELLS; HETEROGENEITY; HOMEOSTASIS; METASTASIS; PHENOTYPE; CHROMATIN; DIVISION; NICHE; ZEB1; MODE;
D O I
10.1016/j.lfs.2019.05.076
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cancer stem cells (CSCs) are self-renewal population localized within cancer niches and play critical roles in tumor initiation, recurrence and metastasis. Despite extensive research, challenges about identity of CSCs and combating them in cancer therapy still remain steady. Cellular plasticity is a cardinal feature of tumor microenvironment (TME) tremendously influencing tumor aggressive behavior. Plasticity and CSC a (symmetry) are interconnecting processes essential for shaping a cancer through nurturing a wide number of cells with tumor promoting capacities. The plastic nature of TME cellularity infers that destemming just CSCs is not sufficient in respect with therapy, especially for high-grade cancers-instead, deploying mechanisms to retard tumor type-dependent TME-CSC interplay is a suggested strategy for making a durable remission of cancer. This requires extending our understanding about CSC divisional profiling and plasticity in order to find critical drivers in cancer progression.
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页数:6
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