Epithelial-to-mesenchymal transition and the cancer stem cell phenotype: insights from cancer biology with therapeutic implications for colorectal cancer

被引:98
|
作者
Findlay, V. J. [1 ]
Wang, C. [2 ]
Watson, D. K. [1 ,3 ,4 ]
Camp, E. R. [2 ,4 ,5 ]
机构
[1] Med Univ S Carolina, Dept Pathol & Lab Med, Charleston, SC 29425 USA
[2] Med Univ S Carolina, Dept Surg, Div Surg Oncol, Charleston, SC 29425 USA
[3] Med Univ S Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[4] Med Univ S Carolina, Hollings Canc Ctr, Charleston, SC 29425 USA
[5] Med Univ S Carolina, Ralph H Johnson VA Med Ctr, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
EPIDERMAL-GROWTH-FACTOR; E-CADHERIN; DOWN-REGULATION; MIR-200; FAMILY; PREOPERATIVE CHEMORADIATION; TUMOR-REGRESSION; DRUG-RESISTANCE; FACTOR RECEPTOR; C-MYC; MICRORNA;
D O I
10.1038/cgt.2014.15
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Although mortality from colorectal cancer (CRC) is decreasing, CRC is still the second highest cause of cancer-related deaths in America. Chemotherapy and radiation therapy now have central roles in our strategies to fight cancer, although we continue to lack novel strategies overcoming therapeutic resistance. Molecular mechanisms of therapeutic resistance in CRC continue to be under intense investigation. In this review, we highlight the recent evidence linking epithelial-to-mesenchynnal transition (EMT) with aggressive tumor biology as well as with the cancer stem cells (CSCs) across multiple organ systems including colon cancer. Furthermore, in the era of neo-adjuvant treatment, the clinical implications are concerning that our treatments may have the potential to induce more aggressive cancer cells through EMT, perhaps even generating CSCs more capable of metastasis and further resistant to treatment. This concern and potential reality highlights the critical need for further understanding the impact of clinical therapy on the pathobiology of cancer and further supports the need to therapeutically target the CSC. Besides serving as potential biomarkers for aggressive tumor biology and therapeutic resistance, EMT and CSC molecular pathways may highlight novel therapeutic targets as strategies for improving the response to conventional anti-neoplastic agents translating into improved oncologic outcomes.
引用
收藏
页码:181 / 187
页数:7
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