Cancer stem cell in breast cancer therapeutic resistance

被引:259
作者
Bai, Xupeng [1 ,2 ]
Ni, Jie [1 ,2 ]
Beretov, Julia [1 ,2 ,3 ]
Graham, Peter [1 ,2 ]
Li, Yong [1 ,2 ,4 ]
机构
[1] St George Hosp, Canc Care Ctr, Kogarah, NSW 2217, Australia
[2] UNSW Sydney, Fac Med, St George & Sutherland Clin Sch, Kensington, NSW 2052, Australia
[3] St George Hosp, NSW Hlth Pathol, Anat Pathol, Kogarah, NSW 2217, Australia
[4] Zhengzhou Univ, Sch Basic Med Sci, Zhengzhou 450001, Henan, Peoples R China
关键词
Breast cancer; Cancer stem cell; Pathway; Resistance; Recurrence; INITIATING CELLS; TUMOR-CELLS; MAMMARY-TUMORS; GROWTH; METASTASIS; PROMOTES; MARKER; EXPRESSION; CD44; IDENTIFICATION;
D O I
10.1016/j.ctrv.2018.07.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Development of therapeutic resistance and metastasis is a major challenge with current breast cancer (BC) therapy. Mounting evidence suggests that a subpopulation of cancer stem cells (CSCs) contribute to the cancer therapeutic resistance and metastasis, leading to the recurrence and death in patients. Breast cancer stem cells (BCSCs) are not only a consequence of mutations that overactivate the self-renewal ability of normal stem cells or committed progenitors but also a result of the de-differentiation of cancer cells induced by somatic mutations or microenvironmental components under treatment. Eradication of BCSCs may bring hope and relief to patients whose lives are threatened by recurrent BCs. Therefore, a better understanding of the generation, regulatory mechanisms, and identification of CSCs in BC therapeutic resistance and metastasis will be imperative for developing BCSC-targeted strategies. Here we summarize the latest studies about cell surface markers and signalling pathways that sustain the sternness of BCSC and discuss the associations of mechanisms behind these traits with phenotype and behavior changes in BCSCs. More importantly, their implications for future study are also evaluated and potential BCSC-targeted strategies are proposed to break through the limitation of current therapies.
引用
收藏
页码:152 / 163
页数:12
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