Notch signaling in lung cancer

被引:5
作者
Galluzzo, Paola
Bocchetta, Maurizio [1 ]
机构
[1] Loyola Univ, Dept Pathol, Chicago Med Ctr, Maywood, IL 60153 USA
关键词
cancer progenitor cells; cancer stem cells; hypoxia; lung cancer; Notch signaling; Notch signaling inhibition; HYPOXIA-INDUCIBLE FACTORS; STEM-CELLS; NEUROENDOCRINE DIFFERENTIATION; PROGENITOR CELLS; SIDE POPULATION; GROWTH; ADENOCARCINOMA; ACTIVATION; PATHWAY; TRANSLOCATION;
D O I
10.1586/ERA.10.158
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the leading cause of cancer-related deaths in the Western world. The lungs can be affected by a number of histologically diverse malignancies. Nonetheless, the vast majority of lung cancers are classified as non-small-cell lung cancer (NSCLC). Despite extensive research on different therapeutic regimens, the overall 5-year survival of patients diagnosed with NSCLC (all stages) is a dismal 15%. Although strongly correlated with tobacco smoke, there is an increasing NSCLC morbidity in individuals who have never smoked. The pattern of genetic lesions found in NSCLC derived from smokers and never-smokers appears to be different. This fact led to the hypothesis that different, still unidentified carcinogens are responsible for lung cancer onset in never-smokers. All the aforementioned considerations compel the scientific community to find novel therapeutic targets to fight such a deadly disease. In recent years critical pathways governing embryonic development have been increasingly linked to cancer. Here we will focus on the role of Notch signaling in lung cancer. Notch receptors' activity can be blocked through the use of different strategies, thus representing a promising alternative/complement to the arsenal of therapeutic strategies currently used to treat lung cancer.
引用
收藏
页码:533 / 540
页数:8
相关论文
共 59 条
[1]  
Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940
[2]   Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760
[3]   ADAM17 Regulates Epidermal Growth Factor Receptor Expression through the Activation of Notch1 in Non-Small Cell Lung Cancer [J].
Baumgart, Anja ;
Seidl, Stefan ;
Vlachou, Petros ;
Michel, Lars ;
Mitova, Nadya ;
Schatz, Nicole ;
Specht, Katja ;
Koch, Ina ;
Schuster, Tibor ;
Grundler, Rebekka ;
Kremer, Marcus ;
Fend, Falko ;
Siveke, Jens T. ;
Peschel, Christian ;
Duyster, Justus ;
Dechow, Tobias .
CANCER RESEARCH, 2010, 70 (13) :5368-5378
[4]   Tumor hypoxia in cancer therapy [J].
Brown, J. Martin .
OXYGEN BIOLOGY AND HYPOXIA, 2007, 435 :297-+
[5]   ABC transporters as phenotypic markers and functional regulators of stem cells [J].
Bunting, KD .
STEM CELLS, 2002, 20 (01) :11-20
[6]   Oxygen concentration determines the biological effects of NOTCH-1 signaling in adenocarcinoma of the lung [J].
Chen, Yuanbin ;
De Marco, Melissa A. ;
Graziani, Irene ;
Gazdar, Adi F. ;
Strack, Peter R. ;
Miele, Lucio ;
Bocchetta, Maurizio .
CANCER RESEARCH, 2007, 67 (17) :7954-7959
[7]   Notch-1 signaling facilitates survivin expression in human non-small cell lung cancer cells [J].
Chen, Yuqing ;
Li, Dianming ;
Liu, Hongli ;
Xu, Huanbai ;
Zheng, Honghua ;
Qian, Feng ;
Li, Wei ;
Zhao, Chengling ;
Wang, Zhenhuan ;
Wang, Xiaojing .
CANCER BIOLOGY & THERAPY, 2011, 11 (01) :14-21
[8]   BIM mediates EGFR tyrosine kinase inhibitor-induced apoptosis in lung cancers with oncogenic EGFR mutations [J].
Costa, Daniel B. ;
Halmos, Balazs ;
Kumar, Amit ;
Schumer, Susan T. ;
Huberman, Mark S. ;
Boggon, Titus J. ;
Tenen, Daniel G. ;
Kobayashi, Susumu .
PLOS MEDICINE, 2007, 4 (10) :1669-1680
[9]   Chromosome 19 translocation, overexpression of Notch3, and human lung cancer [J].
Dang, TP ;
Gazdar, AF ;
Virmani, AK ;
Sepetavec, T ;
Hande, KR ;
Minna, JD ;
Roberts, JR ;
Carbone, DP .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (16) :1355-1357
[10]   Constitutive activation of Notch3 inhibits terminal epithelial differentiation in lungs of transgenic mice [J].
Dang, TP ;
Eichenberger, S ;
Gonzalez, A ;
Olson, S ;
Carbone, DP .
ONCOGENE, 2003, 22 (13) :1988-1997