Stem cells for lung cancer?

被引:74
作者
Berns, A [1 ]
机构
[1] Netherlands Canc Inst, Div Mol Genet, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Ctr Biomed Genet, NL-1066 CX Amsterdam, Netherlands
关键词
D O I
10.1016/j.cell.2005.06.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Stem cells are believed to be crucial players in tumor development. There is much interest in identifying those compartments that harbor stem cells involved in lung cancer, given the high incidence and recurrence rate of this disease. In this issue of Cell, Kim and colleagues describe a niche in the bronchioal-veolar duct junction of adult mouse lung that harbors stem cells from which adenocarcinomas are likely to arise (Kim et al., 2005). They enriched, propagated, and differentiated these stem cells in vitro and found that they were activated by the oncogenic protein K-ras. This study provides exciting insights into how the stem cell compartment operates during both normal lung-tissue homeostasis and the development of lung cancer. The new work offers perspectives on possible therapeutic interventions to combat lung cancer.
引用
收藏
页码:811 / 813
页数:3
相关论文
共 11 条
[1]
Human acute myeloid leukemia is organized as a hierarchy that originates from a primitive hematopoietic cell [J].
Bonnet, D ;
Dick, JE .
NATURE MEDICINE, 1997, 3 (07) :730-737
[2]
Terminal bronchioles harbor a unique airway stem cell population that localizes to the bronchoalveolar duct junction [J].
Giangreco, A ;
Reynolds, SD ;
Stripp, BR .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (01) :173-182
[3]
Tumor induction by an endogenous K-ras oncogene is highly dependent on cellular context [J].
Guerra, C ;
Mijimolle, N ;
Dhawahir, A ;
Dubus, P ;
Barradas, M ;
Serrano, M ;
Campuzano, V ;
Barbacid, M .
CANCER CELL, 2003, 4 (02) :111-120
[4]
Basal cells are a multipotent progenitor capable of renewing the bronchial epithelium [J].
Hong, KU ;
Reynolds, SD ;
Watkins, S ;
Fuchs, E ;
Stripp, BR .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 164 (02) :577-588
[5]
Analysis of lung tumor initiation and progression using conditional expression of oncogenic K-ras [J].
Jackson, EL ;
Willis, N ;
Mercer, K ;
Bronson, RT ;
Crowley, D ;
Montoya, R ;
Jacks, T ;
Tuveson, DA .
GENES & DEVELOPMENT, 2001, 15 (24) :3243-3248
[6]
Chronic versus acute myelogenous leukemia:: A question of self-renewal [J].
Jamieson, CHM ;
Weissman, IL ;
Passegué, E .
CANCER CELL, 2004, 6 (06) :531-533
[7]
KIM CFB, 2005, CELL, P121
[8]
EGFR mutations in lung cancer:: Correlation with clinical response to gefitinib therapy [J].
Paez, JG ;
Jänne, PA ;
Lee, JC ;
Tracy, S ;
Greulich, H ;
Gabriel, S ;
Herman, P ;
Kaye, FJ ;
Lindeman, N ;
Boggon, TJ ;
Naoki, K ;
Sasaki, H ;
Fujii, Y ;
Eck, MJ ;
Sellers, WR ;
Johnson, BE ;
Meyerson, M .
SCIENCE, 2004, 304 (5676) :1497-1500
[9]
Applying the principles of stem-cell biology to cancer [J].
Pardal, R ;
Clarke, MF ;
Morrison, SJ .
NATURE REVIEWS CANCER, 2003, 3 (12) :895-902
[10]
Conditional Clara cell ablation reveals a self-renewing progenitor function of pulmonary neuroendocrine cells [J].
Reynolds, SD ;
Hong, KU ;
Giangreco, A ;
Mango, GW ;
Guron, C ;
Morimoto, Y ;
Stripp, BR .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2000, 278 (06) :L1256-L1263