IL-4-mediated drug resistance in colon cancer stem cells

被引:113
作者
Todaro, Matilde [1 ]
Alea, Mileidys Perez [1 ]
Scopelliti, Alessandro [1 ]
Medema, Jan Paul [2 ]
Stassi, Giorgio [1 ]
机构
[1] Dept Surg & Oncol Sci, Palermo, Italy
[2] Acad Med Ctr, LEXOR Lab Exp Oncol & Radiobiol, Amsterdam, Netherlands
关键词
colon carcinoma; cancer stem cells (CSCs); CD133; musashi-1 (Msi-1); interleukin-4 (IL-4); apoptosis; tumor chemoresistance;
D O I
10.4161/cc.7.3.5389
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cancer stem cells are defined as cells able to both extensively self-renew and differentiate into progenitors. Cancer stem cells are thus likely to be responsible for maintaining or spreading a cancer, and may be the most relevant targets for cancer therapy. The CD133 glycoprotein was recently described as a reliable cancer stem-like cell marker in colon carcinoma. CD133(+) cells are both necessary and sufficient to initiate tumor growth in animal models. The CD133(+) cell population and spheroid cultures contain cells expressing the stem cell marker Musashi-1 which is involved in maintenance of stem cell fate in several tissues and importantly, this expression is maintained in stem-like cells derived from xenografted tumors. Here we discuss the potential use of the CD133 antigen in concert with Musashi-1 as markers to identify the colon cancer stem cell population. Since the upregulation of IL-4 cytokine was recently demonstrated to constitute an important mechanism that protects the tumorigenic CD133(+) cells from apoptosis, the potential benefits of standard chemotherapeutic treatments in combination with IL-4 inhibitors in the context of human colon carcinoma, are also discussed.
引用
收藏
页码:309 / 313
页数:5
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