Identification and expansion of the tumorigenic lung cancer stem cell population

被引:1349
作者
Eramo, A. [1 ]
Lotti, F. [2 ]
Sette, G.
Pilozzi, E. [3 ]
Biffoni, M.
Di Virgilio, A. [4 ]
Conticello, C. [2 ]
Ruco, L.
Peschle, C. [1 ]
De Maria, R. [1 ]
机构
[1] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[2] Mediterranean Inst Oncol, Dept Expt Oncol, Catania, Italy
[3] Univ Roma La Sapienza, St Andreas Hosp, Dept Expt Med, Rome, Italy
[4] Ist Super Sanita, Serv Biotechnol & Anim Welfare, I-00161 Rome, Italy
关键词
cancer stem cells; stem cell markers; lung cancer; CD133; pulmonary stem cells; tumor sphere;
D O I
10.1038/sj.cdd.4402283
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lung carcinoma is often incurable and remains the leading cancer killer in both men and women. Recent evidence indicates that tumors contain a small population of cancer stem cells that are responsible for tumor maintenance and spreading. The identification of the tumorigenic population that sustains lung cancer may contribute significantly to the development of effective therapies. Here, we found that the tumorigenic cells in small cell and non-small cell lung cancer are a rare population of undifferentiated cells expressing CD133, an antigen present in the cell membrane of normal and cancer-primitive cells of the hematopoietic, neural, endothelial and epithelial lineages. Lung cancer CD133(+) cells were able to grow indefinitely as tumor spheres in serum-free medium containing epidermal growth factor and basic fibroblast growth factor. The injection of 10 4 lung cancer CD133(+) cells in immunocompromised mice readily generated tumor xenografts phenotypically identical to the original tumor. Upon differentiation, lung cancer CD133(+) cells acquired the specific lineage markers, while loosing the tumorigenic potential together with CD133 expression. Thus, lung cancer contains a rare population of CD133(+) cancer stem-like cells able to self-renew and generates an unlimited progeny of non-tumorigenic cells. Molecular and functional characterization of such a tumorigenic population may provide valuable information to be exploited in the clinical setting.
引用
收藏
页码:504 / 514
页数:11
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