Guo Wenjun
Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine, Department of Cell Biology, Albert Einstein College of Medicine, New York, New York, USA
Stem Cells Transl Med. 2014 Aug;3(8):942-8. doi: 10.5966/sctm.2014-0020. Epub 2014 Jun 5.
Accumulating evidence has shown that cancer stem cells (CSCs), the cancer cells that have long-term proliferative potential and the ability to regenerate tumors with phenotypically heterogeneous cell types, are important mediators of tumor metastasis and cancer relapse. In breast cancer, these cells often possess attributes of cells that have undergone an epithelial-mesenchymal transition (EMT). Signaling networks mediated by microRNAs and EMT-inducing transcription factors connect the EMT program with the core stem cell regulatory machineries. These signaling networks are also regulated by extrinsic niche signals that induce and maintain CSCs, contributing to metastatic colonization and promoting the reactivation of dormant tumor cells. Targeting these CSC pathways is likely to improve the efficacy of conventional chemo- and radiotherapies.
越来越多的证据表明,癌症干细胞(CSCs),即具有长期增殖潜力且能够再生出具有表型异质性细胞类型肿瘤的癌细胞,是肿瘤转移和癌症复发的重要介质。在乳腺癌中,这些细胞通常具有经历上皮-间质转化(EMT)的细胞的特征。由微小RNA和诱导EMT的转录因子介导的信号网络将EMT程序与核心干细胞调节机制联系起来。这些信号网络也受外在微环境信号的调节,这些信号诱导并维持癌症干细胞,促成转移灶形成并促进休眠肿瘤细胞的重新激活。靶向这些癌症干细胞途径可能会提高传统化疗和放疗的疗效。